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Acute Lung Injury: How Macrophages Orchestrate Resolution of Inflammation and Tissue Repair

https://doi.org/10.3389/fimmu.2011.00065
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1 of the 175 references listed on this page is in the Retraction Watch database as retracted (export 2026-10-21): 10.1056/nejmoa1101324 (notice 2018-10-17).

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Saturated‐efferocytosis generates pro‐resolving CD11b low macrophages: Modulation by resolvins and glucocorticoids
inferredcites →https://doi.org/10.1002/jcb.21142openalex-snapshot
Key developmental regulators change during hyperoxia‐induced injury and recovery in adult mouse lung
inferredcites →https://doi.org/10.1007/978-1-59259-794-9_15openalex-snapshot
TNF-Related Apoptosis-Inducing Ligand (TRAIL)
inferredcites →https://doi.org/10.1007/bf03216395openalex-snapshot
Acute lung injury
inferredcites →https://doi.org/10.1007/s00134-007-0662-7openalex-snapshot
Alveolar fluid clearance in acute lung injury: what have we learned from animal models and clinical studies?
inferredcites →https://doi.org/10.1007/s10495-010-0504-xopenalex-snapshot
Impairment of phagocytosis of apoptotic cells and its role in chronic airway diseases
inferredcites →https://doi.org/10.1007/s10753-011-9337-1openalex-snapshot
Time-Dependent Alterations of VEGF and Its Signaling Molecules in Acute Lung Injury in a Rat Model of Sepsis
inferredcites →https://doi.org/10.1007/s11033-009-9876-9openalex-snapshot
Fas inhibition attenuates lipopolysaccharide-induced apoptosis and cytokine release of rat type II alveolar epithelial cells
inferredcites →https://doi.org/10.1007/s12026-008-8049-6openalex-snapshot
Neutrophil apoptosis and the resolution of infection
inferredcites →https://doi.org/10.1016/j.bbamem.2007.08.018openalex-snapshot
Crosstalk of tight junction components with signaling pathways
inferredcites →https://doi.org/10.1016/j.clim.2010.06.017openalex-snapshot
Alternatively activated alveolar macrophages in pulmonary fibrosis—mediator production and intracellular signal transduction
inferredcites →https://doi.org/10.1016/j.imbio.2011.01.001openalex-snapshot
Macrophages in skin injury and repair
inferredcites →https://doi.org/10.1016/j.immuni.2009.06.024openalex-snapshot
The Kinase Akt1 Controls Macrophage Response to Lipopolysaccharide by Regulating MicroRNAs
inferredcites →https://doi.org/10.1016/j.immuni.2010.05.007openalex-snapshot
Alternative Activation of Macrophages: Mechanism and Functions
inferredcites →https://doi.org/10.1016/j.it.2006.10.004openalex-snapshot
Angiopoietins: a link between angiogenesis and inflammation
inferredcites →https://doi.org/10.1016/j.it.2007.02.007openalex-snapshot
Resolvins and protectins in the termination program of acute inflammation
inferredcites →https://doi.org/10.1016/j.plipres.2010.09.002openalex-snapshot
Resolvins: Natural agonists for resolution of pulmonary inflammation
inferredcites →https://doi.org/10.1016/j.pupt.2011.04.001openalex-snapshot
Resolvin D1 protects mice from LPS-induced acute lung injury
inferredcites →https://doi.org/10.1016/j.smim.2009.01.005openalex-snapshot
Immune homeostasis in the respiratory tract and its impact on heterologous infection
inferredcites →https://doi.org/10.1016/j.stem.2011.05.008openalex-snapshot
Notch and Basal Cells Take Center Stage during Airway Epithelial Regeneration
inferredcites →https://doi.org/10.1016/j.tcb.2003.10.004openalex-snapshot
Cues for apoptotic cell engulfment: eat-me, don't eat-me and come-get-me signals
inferredcites →https://doi.org/10.1016/s0002-9440(10)61175-3openalex-snapshot
Lipoxins Induce Actin Reorganization in Monocytes and Macrophages But Not in Neutrophils
inferredcites →https://doi.org/10.1016/s0002-9440(10)63594-8openalex-snapshot
Transgenic Overexpression of Granulocyte Macrophage-Colony Stimulating Factor in the Lung Prevents Hyperoxic Lung Injury
inferredcites →https://doi.org/10.1016/s0002-9440(10)64455-0openalex-snapshot
Fas and Fas Ligand Are Up-Regulated in Pulmonary Edema Fluid and Lung Tissue of Patients with Acute Lung Injury and the Acute Respiratory Distress Syndrome
inferredcites →https://doi.org/10.1016/s0248-4900(99)90280-0openalex-snapshot
Phagocytosis of apoptotic cells by macrophages
inferredcites →https://doi.org/10.1038/35037722openalex-snapshot
Corpse clearance defines the meaning of cell death
inferredcites →https://doi.org/10.1038/37022openalex-snapshot
Immunosuppressive effects of apoptotic cells
inferredcites →https://doi.org/10.1038/89759openalex-snapshot
Lipid mediator class switching during acute inflammation: signals in resolution
inferredcites →https://doi.org/10.1038/gt.2010.28openalex-snapshot
IL-10 delivery by AAV5 vector attenuates inflammation in mice with pseudomonas pneumonia
inferredcites →https://doi.org/10.1038/mi.2010.6openalex-snapshot
Control of RSV-induced lung injury by alternatively activated macrophages is IL-4Rα-, TLR4-, and IFN-β-dependent
inferredcites →https://doi.org/10.1038/nature05877openalex-snapshot
Resolvin E1 and protectin D1 activate inflammation-resolution programmes
inferredcites →https://doi.org/10.1038/nature06307openalex-snapshot
Identification of Tim4 as a phosphatidylserine receptor
inferredcites →https://doi.org/10.1038/nature08296openalex-snapshot
Nucleotides released by apoptotic cells act as a find-me signal to promote phagocytic clearance
inferredcites →https://doi.org/10.1038/ni.1637openalex-snapshot
A critical function for CD200 in lung immune homeostasis and the severity of influenza infection
inferredcites →https://doi.org/10.1038/ni.1920openalex-snapshot
The Jmjd3-Irf4 axis regulates M2 macrophage polarization and host responses against helminth infection
inferredcites →https://doi.org/10.1038/ni.1990openalex-snapshot
IRF5 promotes inflammatory macrophage polarization and TH1-TH17 responses
inferredcites →https://doi.org/10.1038/nm1770openalex-snapshot
Persistent activation of an innate immune response translates respiratory viral infection into chronic lung disease
inferredcites →https://doi.org/10.1038/nri2294openalex-snapshot
Resolving inflammation: dual anti-inflammatory and pro-resolution lipid mediators
inferredcites →https://doi.org/10.1038/nri2448openalex-snapshot
Exploring the full spectrum of macrophage activation
inferredcites →https://doi.org/10.1038/nri2470openalex-snapshot
Annexin A1 and glucocorticoids as effectors of the resolution of inflammation
inferredcites →https://doi.org/10.1038/nri2779openalex-snapshot
Phagocyte partnership during the onset and resolution of inflammation
inferredcites →https://doi.org/10.1038/nri978openalex-snapshot
Alternative activation of macrophages
inferredcites →https://doi.org/10.1042/cs1040027openalex-snapshot
The inflammatory macrophage: a story of Jekyll and Hyde
inferredcites →https://doi.org/10.1055/s-0031-1272254openalex-snapshot
Exudate macrophages attenuate lung injury by the release of IL-1 receptor antagonist in gram-negative pneumonia
inferredcites →https://doi.org/10.1055/s-2005-925488openalex-snapshot
The inflammatory versus constitutive trafficking of mononuclear phagocytes into the alveolar space of mice is associated with drastic changes in their gene expression profiles
inferredcites →https://doi.org/10.1056/nejmoa1101324openalex-snapshot
RETRACTED: Evidence for Human Lung Stem Cells
inferredcites →https://doi.org/10.1073/pnas.0605298103openalex-snapshot
NF-κB-dependent induction of microRNA miR-146, an inhibitor targeted to signaling proteins of innate immune responses
inferredcites →https://doi.org/10.1073/pnas.0809784106openalex-snapshot
Tolerance and M2 (alternative) macrophage polarization are related processes orchestrated by p50 nuclear factor κB
inferredcites →https://doi.org/10.1073/pnas.0908641106openalex-snapshot
A CREB-C/EBPβ cascade induces M2 macrophage-specific gene expression and promotes muscle injury repair
inferredcites →https://doi.org/10.1073/pnas.0909207107openalex-snapshot
Evidence of an epithelial stem/progenitor cell hierarchy in the adult mouse lung
inferredcites →https://doi.org/10.1073/pnas.1015623108openalex-snapshot
Modulation of cardiac macrophages by phosphatidylserine-presenting liposomes improves infarct repair
inferredcites →https://doi.org/10.1073/pnas.160041997openalex-snapshot
Influenza virus inhibits amiloride-sensitive Na + channels in respiratory epithelia
inferredcites →https://doi.org/10.1073/pnas.202296999openalex-snapshot
Lipoxin A 4 and aspirin-triggered 15-epi-lipoxin A 4 inhibit peroxynitrite formation, NF-κB and AP-1 activation, and IL-8 gene expression in human leukocytes
inferredcites →https://doi.org/10.1074/jbc.272.11.6972openalex-snapshot
Lipoxin A4 Stable Analogs Are Potent Mimetics That Stimulate Human Monocytes and THP-1 Cells via a G-protein-linked Lipoxin A4 Receptor
inferredcites →https://doi.org/10.1074/jbc.m410561200openalex-snapshot
Interleukin-1β Decreases Expression of the Epithelial Sodium Channel α-Subunit in Alveolar Epithelial Cells via a p38 MAPK-dependent Signaling Pathway
inferredcites →https://doi.org/10.1074/jbc.m508342200openalex-snapshot
Apoptotic Cells, at All Stages of the Death Process, Trigger Characteristic Signaling Events That Are Divergent from and Dominant over Those Triggered by Necrotic Cells
inferredcites →https://doi.org/10.1074/jbc.m605146200openalex-snapshot
Apoptotic Cells, through Transforming Growth Factor-β, Coordinately Induce Anti-inflammatory and Suppress Pro-inflammatory Eicosanoid and NO Synthesis in Murine Macrophages
inferredcites →https://doi.org/10.1074/jbc.m706586200openalex-snapshot
Migration to Apoptotic “Find-me” Signals Is Mediated via the Phagocyte Receptor G2A
inferredcites →https://doi.org/10.1080/08916930701357463openalex-snapshot
The affirmative response of the innate immune system to apoptotic cells
inferredcites →https://doi.org/10.1083/jcb1755oia10openalex-snapshot
Oxidized phosphatidylserine–CD36 interactions play an essential role in macrophage-dependent phagocytosis of apoptotic cells
inferredcites →https://doi.org/10.1083/jcb1795oia13openalex-snapshot
The healing myocardium sequentially mobilizes two monocyte subsets with divergent and complementary functions
inferredcites →https://doi.org/10.1084/jem.188.12.2313openalex-snapshot
Complement-dependent Clearance of Apoptotic Cells by Human Macrophages
inferredcites →https://doi.org/10.1084/jem.20020760openalex-snapshot
Resolvins
inferredcites →https://doi.org/10.1084/jem.20041310openalex-snapshot
Role of ChemR23 in directing the migration of myeloid and plasmacytoid dendritic cells to lymphoid organs and inflamed skin
inferredcites →https://doi.org/10.1084/jem.20042031openalex-snapshot
Stereochemical assignment, antiinflammatory properties, and receptor for the omega-3 lipid mediator resolvin E1
inferredcites →https://doi.org/10.1084/jem.20060370openalex-snapshot
Oxidized phosphatidylserine–CD36 interactions play an essential role in macrophage-dependent phagocytosis of apoptotic cells
inferredcites →https://doi.org/10.1084/jem.20070885openalex-snapshot
The healing myocardium sequentially mobilizes two monocyte subsets with divergent and complementary functions
inferredcites →https://doi.org/10.1084/jem.20071601openalex-snapshot
Synthetic chemerin-derived peptides suppress inflammation through ChemR23
inferredcites →https://doi.org/10.1084/jem.20080201openalex-snapshot
Lung epithelial apoptosis in influenza virus pneumonia: the role of macrophage-expressed TNF-related apoptosis-inducing ligand
inferredcites →https://doi.org/10.1084/jem.20081880openalex-snapshot
Maresins: novel macrophage mediators with potent antiinflammatory and proresolving actions
inferredcites →https://doi.org/10.1084/jem.20082048openalex-snapshot
Alternatively activated macrophage-derived RELM-α is a negative regulator of type 2 inflammation in the lung
inferredcites →https://doi.org/10.1084/jem.20082058openalex-snapshot
Efferocytosis impairs pulmonary macrophage and lung antibacterial function via PGE2/EP2 signaling
inferredcites →https://doi.org/10.1084/jem.20101157openalex-snapshot
Find-me and eat-me signals in apoptotic cell clearance: progress and conundrums
inferredcites →https://doi.org/10.1086/500954openalex-snapshot
Functional Tumor Necrosis Factor–Related Apoptosis‐Inducing Ligand Production by Avian Influenza Virus–Infected Macrophages
inferredcites →https://doi.org/10.1091/mbc.12.4.919openalex-snapshot
Distinct Modes of Macrophage Recognition for Apoptotic and Necrotic Cells Are Not Specified Exclusively by Phosphatidylserine Exposure
inferredcites →https://doi.org/10.1096/fasebj.21.5.a131-copenalex-snapshot
Resolvin E1 promotes mucosal surface clearance of neutrophils: a new paradigm for inflammatory resolution
inferredcites →https://doi.org/10.1096/fj.04-1853fjeopenalex-snapshot
Life after corpse engulfment: phagocytosis of apoptotic cells leads to VEGF secretion and cell growth
inferredcites →https://doi.org/10.1096/fj.07-8473comopenalex-snapshot
Resolvin E1 promotes mucosal surface clearance of neutrophils: a new paradigm for inflammatory resolution
inferredcites →https://doi.org/10.1096/fj.10-178939openalex-snapshot
Acute skeletal muscle injury: CCL2 expression by both monocytes and injured muscle is required for repair
inferredcites →https://doi.org/10.1096/fj.10-179473openalex-snapshot
Macrophages programmed by apoptotic cells promote angiogenesis via prostaglandin E 2
inferredcites →https://doi.org/10.1097/01.ccm.0000253811.74112.b6openalex-snapshot
Immunomodulation by n-3- versus n-6-rich lipid emulsions in murine acute lung injury—Role of platelet-activating factor receptor
inferredcites →https://doi.org/10.1111/j.1749-6632.2009.05136.xopenalex-snapshot
New immune pathways from chronic post‐viral lung disease
inferredcites →https://doi.org/10.1113/jphysiol.2006.109579openalex-snapshot
The alveolar type I cells: the new knight of the alveolus?
inferredcites →https://doi.org/10.1124/pr.58.3.4openalex-snapshot
The Lipoxin Receptor ALX: Potent Ligand-Specific and Stereoselective Actions in Vivo
inferredcites →https://doi.org/10.1126/science.1087621openalex-snapshot
Phosphatidylserine Receptor Is Required for Clearance of Apoptotic Cells
inferredcites →https://doi.org/10.1126/science.1142883openalex-snapshot
Monitoring of Blood Vessels and Tissues by a Population of Monocytes with Patrolling Behavior
inferredcites →https://doi.org/10.1126/science.1178331openalex-snapshot
Development of Monocytes, Macrophages, and Dendritic Cells
inferredcites →https://doi.org/10.1126/science.289.5482.1202openalex-snapshot
Inflammation Dampened by Gelatinase A Cleavage of Monocyte Chemoattractant Protein-3
inferredcites →https://doi.org/10.1126/science.294.5548.1871openalex-snapshot
Prostaglandins and Leukotrienes: Advances in Eicosanoid Biology
inferredcites →https://doi.org/10.1128/iai.01270-10openalex-snapshot
Effect of Cytokine Interplay on Macrophage Polarization during Chronic Pulmonary Infection with Cryptococcus neoformans
inferredcites →https://doi.org/10.1136/thx.51.8.781openalex-snapshot
Effect of exposure to silica on human alveolar macrophages in supporting growth activity in type II epithelial cells.
inferredcites →https://doi.org/10.1146/annurev-cellbio-100109-104040openalex-snapshot
Epithelial Progenitor Cells in Lung Development, Maintenance, Repair, and Disease
inferredcites →https://doi.org/10.1146/annurev.immunol.26.021607.090326openalex-snapshot
Monocyte-Mediated Defense Against Microbial Pathogens
inferredcites →https://doi.org/10.1146/annurev.physiol.010908.163250openalex-snapshot
The Contribution of Epithelial Sodium Channels to Alveolar Function in Health and Disease
inferredcites →https://doi.org/10.1152/ajpheart.00235.2002openalex-snapshot
ω-3 Fatty acids suppress monocyte adhesion to human endothelial cells: role of endothelial PAF generation
inferredcites →https://doi.org/10.1152/ajplung.00011.2004openalex-snapshot
Influenza virus inhibits ENaC and lung fluid clearance
inferredcites →https://doi.org/10.1152/ajplung.00016.2006openalex-snapshot
GM-CSF and the impaired pulmonary innate immune response following hyperoxic stress
inferredcites →https://doi.org/10.1152/ajplung.00122.2010openalex-snapshot
New concepts of IL-10-induced lung fibrosis: fibrocyte recruitment and M 2 activation in a CCL2/CCR2 axis
inferredcites →https://doi.org/10.1152/ajplung.00159.2010openalex-snapshot
The Rac1/JNK pathway is critical for EGFR-dependent barrier formation in human airway epithelial cells
inferredcites →https://doi.org/10.1152/ajplung.00361.2009openalex-snapshot
Epithelial repair mechanisms in the lung
inferredcites →https://doi.org/10.1152/ajplung.00525.2007openalex-snapshot
Surface expression of CD74 by type II alveolar epithelial cells: a potential mechanism for macrophage migration inhibitory factor-induced epithelial repair
inferredcites →https://doi.org/10.1152/ajplung.1997.273.4.l715openalex-snapshot
GM-CSF enhances lung growth and causes alveolar type II epithelial cell hyperplasia in transgenic mice
inferredcites →https://doi.org/10.1152/ajplung.90433.2008openalex-snapshot
Genome-wide transcriptional profiling of mononuclear phagocytes recruited to mouse lungs in response to alveolar challenge with the TLR2 agonist Pam3CSK4
inferredcites →https://doi.org/10.1152/ajplung.90453.2008openalex-snapshot
Insulin receptor substrate-1/2 mediates IL-4-induced migration of human airway epithelial cells
inferredcites →https://doi.org/10.1155/2010/634145openalex-snapshot
Role of Bone Marrow-Derived Monocytes/Macrophages in the Repair of Mucosal Damage Caused by Irradiation and/or Anticancer Drugs in Colitis Model
inferredcites →https://doi.org/10.1159/000136335openalex-snapshot
The Role of Neutrophils and Monocytes in Innate Immunity
inferredcites →https://doi.org/10.1161/circresaha.107.161067openalex-snapshot
Interleukin-1β Causes Acute Lung Injury via αvβ5 and αvβ6 Integrin–Dependent Mechanisms
inferredcites →https://doi.org/10.1161/circulationaha.110.978627openalex-snapshot
Early Macrophage Recruitment and Alternative Activation Are Critical for the Later Development of Hypoxia-Induced Pulmonary Hypertension
inferredcites →https://doi.org/10.1164/ajrccm-conference.2011.183.1_meetingabstracts.a2073openalex-snapshot
Rac1/JNK Pathway Is Critical For EGFR-Dependent Barrier Formation In Human Airway Epithelial Cells
inferredcites →https://doi.org/10.1164/ajrccm.163.6.2004035openalex-snapshot
Alveolar Fluid Clearance Is Impaired in the Majority of Patients with Acute Lung Injury and the Acute Respiratory Distress Syndrome
inferredcites →https://doi.org/10.1164/ajrccm.164.10.2104013openalex-snapshot
Cytokine Balance in the Lungs of Patients with Acute Respiratory Distress Syndrome
inferredcites →https://doi.org/10.1164/rccm.200501-155ocopenalex-snapshot
Reactive Species Mediate Inhibition of Alveolar Type II Sodium Transport during Mycoplasma Infection
inferredcites →https://doi.org/10.1164/rccm.200509-1518ocopenalex-snapshot
A Vicious Circle of Alveolar Macrophages and Fibroblasts Perpetuates Pulmonary Fibrosis via CCL18
inferredcites →https://doi.org/10.1164/rccm.200711-1661ocopenalex-snapshot
Surfactant Proteins A and D Suppress Alveolar Macrophage Phagocytosis via Interaction with SIRPα
inferredcites →https://doi.org/10.1164/rccm.200803-455ocopenalex-snapshot
Influenza A Virus Inhibits Alveolar Fluid Clearance in BALB/c Mice
inferredcites →https://doi.org/10.1164/rccm.200807-1064ocopenalex-snapshot
Acute Lung Injury Is Reduced in fat-1 Mice Endogenously Synthesizing n-3 Fatty Acids
inferredcites →https://doi.org/10.1164/rccm.200810-1601ocopenalex-snapshot
15-Epi-lipoxin A4 Inhibits Myeloperoxidase Signaling and Enhances Resolution of Acute Lung Injury
inferredcites →https://doi.org/10.1164/rccm.200811-1794ocopenalex-snapshot
Overexpression of Fibroblast Growth Factor-10 during Both Inflammatory and Fibrotic Phases Attenuates Bleomycin-induced Pulmonary Fibrosis in Mice
inferredcites →https://doi.org/10.1164/rccm.200812-1837ocopenalex-snapshot
Macrophage Tumor Necrosis Factor-α Induces Epithelial Expression of Granulocyte–Macrophage Colony-stimulating Factor: Impact on Alveolar Epithelial Repair
inferredcites →https://doi.org/10.1164/rccm.201002-0181ocopenalex-snapshot
Epithelial Cell Death Is an Important Contributor to Oxidant-mediated Acute Lung Injury
inferredcites →https://doi.org/10.1164/rccm.201009-1431ocopenalex-snapshot
Exudate Macrophages Attenuate Lung Injury by the Release of IL-1 Receptor Antagonist in Gram-negative Pneumonia
inferredcites →https://doi.org/10.1164/rccm.201010-1719ocopenalex-snapshot
Ly6Chi Monocytes Direct Alternatively Activated Profibrotic Macrophage Regulation of Lung Fibrosis
inferredcites →https://doi.org/10.1165/ajrcmb.16.4.9115748openalex-snapshot
Heparin-Binding EGF-Like Growth Factor is a Mitogen for Rat Alveolar Type II Cells
inferredcites →https://doi.org/10.1165/ajrcmb.24.5.4292openalex-snapshot
Alveolar Macrophages that Phagocytose Apoptotic Neutrophils Produce Hepatocyte Growth Factor during Bacterial Pneumonia in Mice
inferredcites →https://doi.org/10.1165/ajrcmb.25.6.4659openalex-snapshot
Interleukin-13 Induces Proliferation of Human Airway Epithelial Cells In Vitro via a Mechanism Mediated by Transforming Growth Factor- α
inferredcites →https://doi.org/10.1165/rcmb.2005-0246ocopenalex-snapshot
Role of Granulocyte Macrophage Colony-Stimulating Factor during Gram-Negative Lung Infection with Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1165/rcmb.2006-0174ocopenalex-snapshot
GM-CSF Regulates a PU.1-Dependent Transcriptional Program Determining the Pulmonary Response to LPS
inferredcites →https://doi.org/10.1165/rcmb.2007-0010ocopenalex-snapshot
PKR Regulates TLR2/TLR4-Dependent Signaling in Murine Alveolar Macrophages
inferredcites →https://doi.org/10.1165/rcmb.2008-0423ocopenalex-snapshot
MCP-1 Antibody Treatment Enhances Damage and Impedes Repair of the Alveolar Epithelium in Influenza Pneumonitis
inferredcites →https://doi.org/10.1165/rcmb.2009-0100ocopenalex-snapshot
Potential Role of Soluble TRAIL in Epithelial Injury in Children with Severe RSV Infection
inferredcites →https://doi.org/10.1165/rcmb.2010-0471ocopenalex-snapshot
Recruited Exudative Macrophages Selectively Produce CXCL10 after Noninfectious Lung Injury
inferredcites →https://doi.org/10.1172/jci1112openalex-snapshot
Macrophages that have ingested apoptotic cells in vitro inhibit proinflammatory cytokine production through autocrine/paracrine mechanisms involving TGF-beta, PGE2, and PAF.
inferredcites →https://doi.org/10.1172/jci116673openalex-snapshot
Keratinocyte growth factor and hepatocyte growth factor/scatter factor are heparin-binding growth factors for alveolar type II cells in fibroblast-conditioned medium.
inferredcites →https://doi.org/10.1172/jci30595openalex-snapshot
Infectious disease, the innate immune response, and fibrosis
inferredcites →https://doi.org/10.1172/jci36150openalex-snapshot
Macrophage diversity in renal injury and repair
inferredcites →https://doi.org/10.1172/jci36498openalex-snapshot
CD4+CD25+Foxp3+ Tregs resolve experimental lung injury in mice and are present in humans with acute lung injury
inferredcites →https://doi.org/10.1172/jci45444openalex-snapshot
Krüppel-like factor 4 regulates macrophage polarization
inferredcites →https://doi.org/10.1172/jci57673openalex-snapshot
Integrin α6β4 identifies an adult distal lung epithelial population with regenerative potential in mice
inferredcites →https://doi.org/10.1177/1753425910369271openalex-snapshot
Review: Soluble innate immune pattern-recognition proteins for clearing dying cells and cellular components: implications on exacerbating or resolving inflammation
inferredcites →https://doi.org/10.1182/blood-2002-04-1102openalex-snapshot
GM-CSF, via PU.1, regulates alveolar macrophage FcγR-mediated phagocytosis and the IL-18/IFN-γ–mediated molecular connection between innate and adaptive immunity in the lung
inferredcites →https://doi.org/10.1182/blood-2007-12-129080openalex-snapshot
Macrophage-specific metalloelastase (MMP-12) truncates and inactivates ELR+ CXC chemokines and generates CCL2, -7, -8, and -13 antagonists: potential role of the macrophage in terminating polymorphonuclear leukocyte influx
inferredcites →https://doi.org/10.1182/blood-2008-06-162404openalex-snapshot
CX3CL1/fractalkine is released from apoptotic lymphocytes to stimulate macrophage chemotaxis
inferredcites →https://doi.org/10.1182/blood-2009-04-217620openalex-snapshot
Epigenetic regulation of the alternatively activated macrophage phenotype
inferredcites →https://doi.org/10.1182/blood.v100.4.1160.h81602001160_1160_1167openalex-snapshot
Matrix metalloproteinase processing of monocyte chemoattractant proteins generates CC chemokine receptor antagonists with anti-inflammatory properties in vivo
inferredcites →https://doi.org/10.1183/09031936.98.11030534openalex-snapshot
Expression of pro-inflammatory cytokines by flow-sorted alveolar macrophages in severe pneumonia
inferredcites →https://doi.org/10.1186/cc5042openalex-snapshot
The early responses of VEGF and its receptors during acute lung injury: implication of VEGF in alveolar epithelial cell survival
inferredcites →https://doi.org/10.1186/rr36openalex-snapshot
Alveolar epithelial type II cell: defender of the alveolus revisited
inferredcites →https://doi.org/10.1189/jlb.0211062openalex-snapshot
TNF-related apoptosis-inducing ligand (TRAIL) regulates inflammatory neutrophil apoptosis and enhances resolution of inflammation
inferredcites →https://doi.org/10.1203/00006450-200009000-00007openalex-snapshot
Preventing Endotoxin-Stimulated Alveolar Macrophages from Decreasing Epithelium Na+ Channel (ENaC) mRNA Levels and Activity
inferredcites →https://doi.org/10.1371/journal.ppat.1001304openalex-snapshot
Type I Interferon Signaling Regulates Ly6Chi Monocytes and Neutrophils during Acute Viral Pneumonia in Mice
inferredcites →https://doi.org/10.1378/chest.120.1_suppl.s60openalex-snapshot
Transforming Growth Factor-β1 Modifies Fibroblast Growth Factor-2 Production in Type II Cells
inferredcites →https://doi.org/10.1513/pats.200502-012acopenalex-snapshot
Protection of Epithelial Cells by Keratincoyte Growth Factor Signaling
inferredcites →https://doi.org/10.1513/pats.200710-160dropenalex-snapshot
What Differentiates Normal Lung Repair and Fibrosis?: Inflammation, Resolution of Repair, and Fibrosis
inferredcites →https://doi.org/10.1513/pats.200801-011awopenalex-snapshot
Hierarchical Organization of Lung Progenitor Cells: Is there An Adult Lung Tissue Stem Cell?
inferredcites →https://doi.org/10.1681/asn.2009060615openalex-snapshot
Distinct Macrophage Phenotypes Contribute to Kidney Injury and Repair
inferredcites →https://doi.org/10.2119/molmed.2011.00129openalex-snapshot
Myeloid Angiogenic Cells Act as Alternative M2 Macrophages and Modulate Angiogenesis through Interleukin-8
inferredcites →https://doi.org/10.2174/1389210204504764501openalex-snapshot
Airway Clearance of Apoptotic Cells in Copd
inferredcites →https://doi.org/10.2174/138945011794751609openalex-snapshot
Airway Clearance of Apoptotic Cells in COPD
inferredcites →https://doi.org/10.2741/2692openalex-snapshot
Macrophage activation and polarization
inferredcites →https://doi.org/10.3109/01902149709039233openalex-snapshot
Enhanced Production of an Egf-Like Growth Factor by Parenchymal Macrophages Following Bleomycin-Induced Pulmonary Injury
inferredcites →https://doi.org/10.4049/jimmunol.0901037openalex-snapshot
Mouse ChemR23 Is Expressed in Dendritic Cell Subsets and Macrophages, and Mediates an Anti-Inflammatory Activity of Chemerin in a Lung Disease Model
inferredcites →https://doi.org/10.4049/jimmunol.0901809openalex-snapshot
The Anti-Inflammatory and Proresolving Mediator Resolvin E1 Protects Mice from Bacterial Pneumonia and Acute Lung Injury
inferredcites →https://doi.org/10.4049/jimmunol.0902501openalex-snapshot
Production of Vascular Endothelial Growth Factors from Human Lung Macrophages Induced by Group IIA and Group X Secreted Phospholipases A2
inferredcites →https://doi.org/10.4049/jimmunol.0903378openalex-snapshot
Chemerin Peptides Promote Phagocytosis in a ChemR23- and Syk-Dependent Manner
inferredcites →https://doi.org/10.4049/jimmunol.164.4.1663openalex-snapshot
Cutting Edge: Lipoxins Rapidly Stimulate Nonphlogistic Phagocytosis of Apoptotic Neutrophils by Monocyte-Derived Macrophages
inferredcites →https://doi.org/10.4049/jimmunol.169.2.702openalex-snapshot
Phagocytosis of Apoptotic Cells by Macrophages Induces Novel Signaling Events Leading to Cytokine-Independent Survival and Inhibition of Proliferation: Activation of Akt and Inhibition of Extracellular Signal-Regulated Kinases 1 and 2
inferredcites →https://doi.org/10.4049/jimmunol.172.1.398openalex-snapshot
Essential Contribution of Monocyte Chemoattractant Protein-1/C-C Chemokine Ligand-2 to Resolution and Repair Processes in Acute Bacterial Pneumonia
inferredcites →https://doi.org/10.4049/jimmunol.172.2.880openalex-snapshot
Innate Immune Discrimination of Apoptotic Cells: Repression of Proinflammatory Macrophage Transcription Is Coupled Directly to Specific Recognition
inferredcites →https://doi.org/10.4049/jimmunol.175.3.1884openalex-snapshot
The Inflammatory versus Constitutive Trafficking of Mononuclear Phagocytes into the Alveolar Space of Mice Is Associated with Drastic Changes in Their Gene Expression Profiles
inferredcites →https://doi.org/10.4049/jimmunol.177.3.1817openalex-snapshot
Alveolar Epithelial Cells Direct Monocyte Transepithelial Migration upon Influenza Virus Infection: Impact of Chemokines and Adhesion Molecules
inferredcites →https://doi.org/10.4049/jimmunol.178.4.2000openalex-snapshot
Distinct Differentiation Potential of Blood Monocyte Subsets in the Lung
inferredcites →https://doi.org/10.4049/jimmunol.178.6.3912openalex-snapshot
Resolvin E1 Selectively Interacts with Leukotriene B4 Receptor BLT1 and ChemR23 to Regulate Inflammation
inferredcites →https://doi.org/10.4049/jimmunol.178.8.5001openalex-snapshot
Protective Role of Macrophages in Noninflammatory Lung Injury Caused by Selective Ablation of Alveolar Epithelial Type II Cells
inferredcites →https://doi.org/10.4049/jimmunol.179.8.5082openalex-snapshot
Modulation of miR-155 and miR-125b Levels following Lipopolysaccharide/TNF-α Stimulation and Their Possible Roles in Regulating the Response to Endotoxin Shock
inferredcites →https://doi.org/10.4049/jimmunol.181.6.3733openalex-snapshot
Macrophage Polarization in Bacterial Infections

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Comparison of treatment of COVID-19 with inhaled bromhexine, higher doses of colchicine and hymecromone with WHO-recommended paxlovid, molnupiravir, remdesivir, anti-IL-6 receptor antibodies and baricitinib
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Pharmacoengineering of Lipid Nanoarchitectonics in Modulating Particle Uptake by Lung Macrophages
inferred← citeshttps://doi.org/10.1002/adhm.202500695openalex-snapshot
Pulmonary Delivery of siRNA Anti‐TNFα‐loaded Lipid Nanoparticles for Rapid Recovery in Murine Acute Lung Injury
inferred← citeshttps://doi.org/10.1002/advs.202406060openalex-snapshot
ROS‐Driven Nanoventilator for MRSA‐Induced Acute Lung Injury Treatment via In Situ Oxygen Supply, Anti‐Inflammation and Immunomodulation
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Peroxisome proliferator‐activated receptor gamma coactivator‐1α/HSF1 axis effectively alleviates lipopolysaccharide‐induced acute lung injury via suppressing oxidative stress and inflammatory response
inferred← citeshttps://doi.org/10.1002/jcp.25316openalex-snapshot
MicroRNA Regulation of Acute Lung Injury and Acute Respiratory Distress Syndrome
inferred← citeshttps://doi.org/10.1002/jcp.29504openalex-snapshot
MicroRNA‐182 supplies negative feedback regulation to ameliorate lipopolysaccharide‐induced ALI in mice by targeting TLR4
inferred← citeshttps://doi.org/10.1002/mco2.70074openalex-snapshot
Acute respiratory distress syndrome (ARDS): from mechanistic insights to therapeutic strategies
inferred← citeshttps://doi.org/10.1002/ppul.23984openalex-snapshot
Airway cells from protracted bacterial bronchitis and bronchiectasis share similar gene expression profiles
inferred← citeshttps://doi.org/10.1002/ptr.7131openalex-snapshot
New perspectives on natural flavonoids on COVID ‐19‐induced lung injuries
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Solid Organ Injury
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The Inflammatory and Barrier Response After Polytrauma
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The Pathogenetic Role of DAMPs in Severe Infectious Diseases
inferred← citeshttps://doi.org/10.1007/978-3-031-55858-0_118-1openalex-snapshot
Antimicrobial Blue Light Photoinactivation of Lung Infections
inferred← citeshttps://doi.org/10.1007/978-3-031-65944-7_10openalex-snapshot
Macrophages in Lung Repair and Fibrosis
inferred← citeshttps://doi.org/10.1007/978-3-0348-0977-1_3openalex-snapshot
Idiopathic Pulmonary Fibrosis
inferred← citeshttps://doi.org/10.1007/978-3-319-64597-1_94-1openalex-snapshot
Monocytes and Macrophages in the Aged Lung and Heart
inferred← citeshttps://doi.org/10.1007/978-3-319-99375-1_94openalex-snapshot
Monocytes and Macrophages in the Aged Lung and Heart
inferred← citeshttps://doi.org/10.1007/s00011-020-01378-2openalex-snapshot
Macrophage polarization and its role in the pathogenesis of acute lung injury/acute respiratory distress syndrome
inferred← citeshttps://doi.org/10.1007/s00109-020-01961-4openalex-snapshot
Immuno-epidemiology and pathophysiology of coronavirus disease 2019 (COVID-19)
inferred← citeshttps://doi.org/10.1007/s00210-023-02501-wopenalex-snapshot
Effect of saffron, black seed, and their main constituents on inflammatory cytokine response (mainly TNF-α) and oxidative stress status: an aspect on pharmacological insights
inferred← citeshttps://doi.org/10.1007/s00428-021-03053-1openalex-snapshot
The pulmonary pathology of COVID-19
inferred← citeshttps://doi.org/10.1007/s00441-016-2521-8openalex-snapshot
Lung remodeling associated with recovery from acute lung injury
inferred← citeshttps://doi.org/10.1007/s10068-026-02140-wopenalex-snapshot
The inhibitory effects of Melicope pahangenesis T. G. Hartley extract on LPS-induced acute lung injury
inferred← citeshttps://doi.org/10.1007/s10439-013-0891-6openalex-snapshot
The Autodigestion Hypothesis for Shock and Multi-organ Failure
inferred← citeshttps://doi.org/10.1007/s10753-022-01692-3openalex-snapshot
Macrophage-Targeted Nanomedicines for ARDS/ALI: Promise and Potential
inferred← citeshttps://doi.org/10.1007/s10753-022-01726-wopenalex-snapshot
The Role of Macrophages and Alveolar Epithelial Cells in the Development of ARDS
inferred← citeshttps://doi.org/10.1007/s10787-017-0371-yopenalex-snapshot
Carbon monoxide-releasing molecule, CORM-3, modulates alveolar macrophage M1/M2 phenotype in vitro
inferred← citeshttps://doi.org/10.1007/s10787-026-02414-zopenalex-snapshot
Macrophage polarization plasticity in pulmonary fibrosis: a review from pathogenesis to therapeutic targeting
inferred← citeshttps://doi.org/10.1007/s11427-020-1902-3openalex-snapshot
The diversity of adult lung epithelial stem cells and their niche in homeostasis and regeneration
inferred← citeshttps://doi.org/10.1007/s12026-026-09789-9openalex-snapshot
ProBDNF promotes LPS-induced pro-inflammatory polarization of alveolar macrophages via the Notch1 signaling pathway
inferred← citeshttps://doi.org/10.1007/s12032-013-0774-6openalex-snapshot
Granulocyte–macrophage colony-stimulating factor: not just another haematopoietic growth factor
inferred← citeshttps://doi.org/10.1007/s12272-016-0716-xopenalex-snapshot
Protective effect of sesquiterpene lactone parthenolide on LPS-induced acute lung injury
inferred← citeshttps://doi.org/10.1007/s12325-022-02395-9openalex-snapshot
What Do We Need to Know About Rising Rates of Idiopathic Pulmonary Fibrosis? A Narrative Review and Update
inferred← citeshttps://doi.org/10.1016/b978-0-12-404577-4.00032-1openalex-snapshot
Pulmonary Macrophages
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.62165-7openalex-snapshot
Aging Lung
inferred← citeshttps://doi.org/10.1016/b978-0-323-95488-4.00238-2openalex-snapshot
Inflammatory Cells of the Lung: Macrophages
inferred← citeshttps://doi.org/10.1016/j.actbio.2024.03.031openalex-snapshot
Immunometabolic reprogramming of macrophages with inhalable CRISPR/Cas9 nanotherapeutics for acute lung injury intervention
inferred← citeshttps://doi.org/10.1016/j.ajpath.2014.09.005openalex-snapshot
In Vivo Depletion of CD206+ M2 Macrophages Exaggerates Lung Injury in Endotoxemic Mice
inferred← citeshttps://doi.org/10.1016/j.ajpath.2018.01.020openalex-snapshot
Trefoil Factor 2 Promotes Type 2 Immunity and Lung Repair through Intrinsic Roles in Hematopoietic and Nonhematopoietic Cells
inferred← citeshttps://doi.org/10.1016/j.ajpath.2018.02.004openalex-snapshot
The Four-and-a-Half LIM Domain Protein 2 Supports Influenza A Virus–Induced Lung Inflammation by Restricting the Host Adaptive Immune Response
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Alcohol and inflammatory responses: Summary of the 2013 Alcohol and Immunology Research Interest Group (AIRIG) meeting
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Alcohol and lung injury and immunity
inferred← citeshttps://doi.org/10.1016/j.alcohol.2018.09.001openalex-snapshot
Mesenchymal stem cell treatment attenuates liver and lung inflammation after ethanol intoxication and burn injury
inferred← citeshttps://doi.org/10.1016/j.bbrc.2018.04.161openalex-snapshot
Nrf2 activation protects against intratracheal LPS induced mouse/murine acute respiratory distress syndrome by regulating macrophage polarization
inferred← citeshttps://doi.org/10.1016/j.bcp.2018.12.010openalex-snapshot
Lung cancer stem cells: origin, features, maintenance mechanisms and therapeutic targeting
inferred← citeshttps://doi.org/10.1016/j.biocel.2024.106651openalex-snapshot
QSOX1 exerts anti-inflammatory effects in sepsis-induced acute lung injury: Regulation involving EGFR phosphorylation mediated M1 polarization of macrophages
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2013.09.103openalex-snapshot
Enhancement of bone regeneration by dual release of a macrophage recruitment agent and platelet-rich plasma from gelatin hydrogels
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2021.120986openalex-snapshot
A bilirubin-derived nanomedicine attenuates the pathological cascade of pulmonary fibrosis
inferred← citeshttps://doi.org/10.1016/j.biopha.2019.108748openalex-snapshot
Emerging role of extracellular vesicles in lung injury and inflammation
inferred← citeshttps://doi.org/10.1016/j.biopha.2020.109995openalex-snapshot
Amphiregulin inhibits TNF-α-induced alveolar epithelial cell death through EGFR signaling pathway
inferred← citeshttps://doi.org/10.1016/j.biopha.2021.111949openalex-snapshot
Salidroside attenuates acute lung injury via inhibition of inflammatory cytokine production
inferred← citeshttps://doi.org/10.1016/j.biopha.2024.117704openalex-snapshot
TNF signaling mediates lipopolysaccharide-induced lung epithelial progenitor cell responses in mouse lung organoids
inferred← citeshttps://doi.org/10.1016/j.celrep.2018.02.071openalex-snapshot
Telomere Dysfunction Disturbs Macrophage Mitochondrial Metabolism and the NLRP3 Inflammasome through the PGC-1α/TNFAIP3 Axis
inferred← citeshttps://doi.org/10.1016/j.celrep.2019.03.053openalex-snapshot
PAR2-Mediated cAMP Generation Suppresses TRPV4-Dependent Ca2+ Signaling in Alveolar Macrophages to Resolve TLR4-Induced Inflammation
inferred← citeshttps://doi.org/10.1016/j.cger.2017.06.002openalex-snapshot
Inflammaging and the Lung
inferred← citeshttps://doi.org/10.1016/j.clim.2021.108731openalex-snapshot
Invasive fungal disease and the immunocompromised host including allogeneic hematopoietic cell transplant recipients: Improved understanding and new strategic approach with sargramostim
inferred← citeshttps://doi.org/10.1016/j.colsurfb.2026.116115openalex-snapshot
Inhalable biomimetic apoptotic bodies enable targeted LXRα agonist delivery to lung macrophages for acute lung injury therapy
inferred← citeshttps://doi.org/10.1016/j.compbiomed.2025.111015openalex-snapshot
Modeling inflammation in allergic asthma: Exploring the role of mesenchymal stem cells in therapeutic strategies
inferred← citeshttps://doi.org/10.1016/j.cytogfr.2020.11.003openalex-snapshot
Macrophage-derived cytokines in pneumonia: Linking cellular immunology and genetics
inferred← citeshttps://doi.org/10.1016/j.drudis.2016.08.006openalex-snapshot
Macrophage polarization in response to epigenetic modifiers during infection and inflammation
inferred← citeshttps://doi.org/10.1016/j.drup.2024.101115openalex-snapshot
Dynamic immunoediting by macrophages in homologous recombination deficiency-stratified pancreatic ductal adenocarcinoma
inferred← citeshttps://doi.org/10.1016/j.ejpb.2022.11.017openalex-snapshot
Inhalation of L-arginine-modified liposomes targeting M1 macrophages to enhance curcumin therapeutic efficacy in ALI
inferred← citeshttps://doi.org/10.1016/j.etp.2013.02.004openalex-snapshot
Toxicological effects of cigarette smoke on Ana-1 macrophages in vitro
inferred← citeshttps://doi.org/10.1016/j.fitote.2025.106572openalex-snapshot
Liang-Ge-San drives macrophages toward M2 polarization for alleviating lipopolysaccharide-induced acute lung injury via activating the miR-21/PTEN axis
inferred← citeshttps://doi.org/10.1016/j.healun.2022.05.005openalex-snapshot
Interferon-stimulated and metallothionein-expressing macrophages are associated with acute and chronic allograft dysfunction after lung transplantation
inferred← citeshttps://doi.org/10.1016/j.ibmb.2023.103960openalex-snapshot
The tracheal immune system of insects - A blueprint for understanding epithelial immunity
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.135077openalex-snapshot
RETRACTED: Potential diagnostic biomarkers and Mapk14 protein expression: Autophagy-related genes linking immune infiltration in acute respiratory distress syndrome
inferred← citeshttps://doi.org/10.1016/j.imbio.2017.11.001openalex-snapshot
Macrophages: Their role, activation and polarization in pulmonary diseases
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TRIM59 alleviates acute respiratory distress syndrome by regulating inflammatory cytokines through RING domain
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Biology of lung macrophages in health and disease
inferred← citeshttps://doi.org/10.1016/j.injury.2022.04.009openalex-snapshot
Pathophysiology in patients with polytrauma
inferred← citeshttps://doi.org/10.1016/j.intimp.2018.03.029openalex-snapshot
C5a receptor1 inhibition alleviates influenza virus-induced acute lung injury
inferred← citeshttps://doi.org/10.1016/j.intimp.2019.02.005openalex-snapshot
BML-111 accelerates the resolution of inflammation by modulating the Nrf2/HO-1 and NF-κB pathways in rats with ventilator-induced lung injury
inferred← citeshttps://doi.org/10.1016/j.intimp.2019.105741openalex-snapshot
MCP-induced protein 1 attenuates sepsis-induced acute lung injury by modulating macrophage polarization via the JNK/c-Myc pathway
inferred← citeshttps://doi.org/10.1016/j.intimp.2022.108944openalex-snapshot
ACT001 suppressing M1 polarization against inflammation via NF-κB and STAT1 signaling pathways alleviates acute lung injury in mice
inferred← citeshttps://doi.org/10.1016/j.intimp.2023.110693openalex-snapshot
HSF1 enhances the attenuation of exosomes from mesenchymal stem cells to hemorrhagic shock induced lung injury by altering the protein profile of exosomes
inferred← citeshttps://doi.org/10.1016/j.intimp.2024.111991openalex-snapshot
Targeting BRD4 with PROTAC degrader ameliorates LPS-induced acute lung injury by inhibiting M1 alveolar macrophage polarization
inferred← citeshttps://doi.org/10.1016/j.intimp.2024.113674openalex-snapshot
Pharmacological inhibition of P300 with C646 ameliorates LPS-induced acute lung injury by modulating CXCL1 in M1 alveolar macrophages
inferred← citeshttps://doi.org/10.1016/j.jaci.2015.11.012openalex-snapshot
Activated prostaglandin D2 receptors on macrophages enhance neutrophil recruitment into the lung
inferred← citeshttps://doi.org/10.1016/j.jconrel.2020.06.036openalex-snapshot
Mesenchymal stromal cells and their secreted extracellular vesicles as therapeutic tools for COVID-19 pneumonia?
inferred← citeshttps://doi.org/10.1016/j.jep.2017.08.028openalex-snapshot
Anti-inflammatory effect of stem bark of Paulownia tomentosa Steud. in lipopolysaccharide (LPS)-stimulated RAW264.7 macrophages and LPS-induced murine model of acute lung injury
inferred← citeshttps://doi.org/10.1016/j.jep.2025.120683openalex-snapshot
Mechanism of Reynoutria Japonica Houtt and its active component luteolin in treating acute lung injury by targeting AKT1 to inhibit macrophage apoptosis and mitochondrial damage
inferred← citeshttps://doi.org/10.1016/j.jiac.2024.08.015openalex-snapshot
The suppression of nuclear factor kappa B/microRNA 222 axis alleviates lipopolysaccharide-induced acute lung injury through increasing the alkylglyceronephosphate synthase expression
inferred← citeshttps://doi.org/10.1016/j.jprot.2019.103451openalex-snapshot
Proteomic analysis of bronchoalveolar lavage fluid in rat exposed to TiO2 nanostructured aerosol by inhalation
inferred← citeshttps://doi.org/10.1016/j.jss.2020.06.062openalex-snapshot
Maresin1 Promotes M2 Macrophage Polarization Through Peroxisome Proliferator–Activated Receptor-γ Activation to Expedite Resolution of Acute Lung Injury
inferred← citeshttps://doi.org/10.1016/j.jtbi.2021.110738openalex-snapshot
Mathematical modeling of ventilator-induced lung inflammation
inferred← citeshttps://doi.org/10.1016/j.lfs.2020.117415openalex-snapshot
High-mobility group box 1 protein participates in acute lung injury by activating protein kinase R and inducing M1 polarization
inferred← citeshttps://doi.org/10.1016/j.lfs.2020.119010openalex-snapshot
Monocytes and macrophages in COVID-19: Friends and foes
inferred← citeshttps://doi.org/10.1016/j.micinf.2014.07.005openalex-snapshot
mTOR and autophagy in regulation of acute lung injury: a review and perspective
inferred← citeshttps://doi.org/10.1016/j.micpath.2023.106463openalex-snapshot
Amphiregulin in infectious diseases: Role, mechanism, and potential therapeutic targets
inferred← citeshttps://doi.org/10.1016/j.micpath.2023.106483openalex-snapshot
The long-lasting Ascaris suum antigens in the lungs shapes the tissue adaptation modifying the pulmonary architecture and immune response after infection in mice
inferred← citeshttps://doi.org/10.1016/j.molimm.2019.04.033openalex-snapshot
Chronic and low-level particulate matter exposure can sustainably mediate lung damage and alter CD4 T cells during acute lung injury
inferred← citeshttps://doi.org/10.1016/j.mucimm.2024.08.008openalex-snapshot
Deciphering the therapeutic potential of Myeloid-Specific JAK2 inhibition in acute respiratory distress syndrome
inferred← citeshttps://doi.org/10.1016/j.pharep.2016.09.021openalex-snapshot
Diethylcarbamazine attenuates LPS-induced acute lung injury in mice by apoptosis of inflammatory cells
inferred← citeshttps://doi.org/10.1016/j.pt.2017.12.007openalex-snapshot
Helminth Modulation of Lung Inflammation
inferred← citeshttps://doi.org/10.1016/j.redox.2024.103059openalex-snapshot
A novel role for the ROS-ATM-Chk2 axis mediated metabolic and cell cycle reprogramming in the M1 macrophage polarization
inferred← citeshttps://doi.org/10.1016/j.redox.2026.104337openalex-snapshot
Novel mitophagy activator TJ0113 restricts cytosolic mtDNA to suppress ZBP1-driven inflammation in acute lung injury
inferred← citeshttps://doi.org/10.1016/j.resp.2025.104451openalex-snapshot
Chrysin-loaded PLGA nanoparticle attenuates ferroptosis in lipopolysaccharide-induced indirect acute lung injury by upregulating Nrf2-dependent antioxidant responses
inferred← citeshttps://doi.org/10.1016/j.semcdb.2016.08.006openalex-snapshot
Tissue-specific contribution of macrophages to wound healing
inferred← citeshttps://doi.org/10.1016/j.stem.2017.03.024openalex-snapshot
Recruited Monocytes and Type 2 Immunity Promote Lung Regeneration following Pneumonectomy
inferred← citeshttps://doi.org/10.1016/j.taap.2018.04.033openalex-snapshot
Evaluation of the dose-response and fate in the lung and pleura of chrysotile-containing brake dust compared to chrysotile or crocidolite asbestos in a 28-day quantitative inhalation toxicology study
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Evaluating opportunities for advancing the use of alternative methods in risk assessment through the development of fit-for-purpose in vitro assays
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Single tire-derived pollutant (6-PPD) exposure triggers lung injury and mitochondrial disruption in mice
inferred← citeshttps://doi.org/10.1016/j.toxlet.2020.07.035openalex-snapshot
A review of Sulfur Mustard-induced pulmonary immunopathology: An Alveolar Macrophage Approach
inferred← citeshttps://doi.org/10.1016/j.toxlet.2020.11.006openalex-snapshot
Comparison of the biological impact of aerosol of e-vapor device with MESH® technology and cigarette smoke on human bronchial and alveolar cultures
inferred← citeshttps://doi.org/10.1016/j.trsl.2024.05.012openalex-snapshot
Interplay between pulmonary epithelial stem cells and innate immune cells contribute to the repair and regeneration of ALI/ARDS
inferred← citeshttps://doi.org/10.1016/j.vetimm.2021.110378openalex-snapshot
Interferon gamma, lipopolysaccharide, and modified-live viral vaccines stimulation alter the mRNA expression of tumor necrosis factor α, inducible nitric oxide synthase, and interferon β in bovine alveolar macrophages
inferred← citeshttps://doi.org/10.1016/j.ymthe.2023.01.003openalex-snapshot
Peptide-guided delivery improves the therapeutic efficacy and safety of glucocorticoid drugs for treating acute lung injury
inferred← citeshttps://doi.org/10.1021/acs.biomac.1c01447openalex-snapshot
Inhalable SARS-CoV-2 Mimetic Particles Induce Pleiotropic Antigen Presentation
inferred← citeshttps://doi.org/10.1021/acs.biomac.7b00572openalex-snapshot
Anti-Inflammatory Effect of Anti-TNF-α SiRNA Cationic Phosphorus Dendrimer Nanocomplexes Administered Intranasally in a Murine Acute Lung Injury Model
inferred← citeshttps://doi.org/10.1021/acs.est.2c09024openalex-snapshot
PM 2.5 Increases Systemic Inflammatory Cells and Associated Disease Risks by Inducing NRF2-Dependent Myeloid-Biased Hematopoiesis in Adult Male Mice
inferred← citeshttps://doi.org/10.1021/acs.jafc.5c00077openalex-snapshot
Malvidin Alleviates Lipopolysaccharide-Induced Acute Lung Injury by Modulating JAK2/STAT3 Signaling to Inhibit Macrophage M1 Polarization and Oxidative Stress
inferred← citeshttps://doi.org/10.1021/acsnano.6b07895openalex-snapshot
Pro-Inflammatory and Pro-Fibrogenic Effects of Ionic and Particulate Arsenide and Indium-Containing Semiconductor Materials in the Murine Lung
inferred← citeshttps://doi.org/10.1038/s41385-020-0321-7openalex-snapshot
Regulatory role of Gpr84 in the switch of alveolar macrophages from CD11blo to CD11bhi status during lung injury process
inferred← citeshttps://doi.org/10.1038/s41416-021-01309-wopenalex-snapshot
Cancer metastasis as a non-healing wound
inferred← citeshttps://doi.org/10.1038/s41419-019-1900-yopenalex-snapshot
Efficacy of pulmonary transplantation of engineered macrophages secreting IL-4 on acute lung injury in C57BL/6J mice
inferred← citeshttps://doi.org/10.1038/s41419-020-03320-0openalex-snapshot
The HIV protease inhibitor Saquinavir attenuates sepsis-induced acute lung injury and promotes M2 macrophage polarization via targeting matrix metalloproteinase-9
inferred← citeshttps://doi.org/10.1038/s41435-021-00140-wopenalex-snapshot
Role of DAMPs in respiratory virus-induced acute respiratory distress syndrome—with a preliminary reference to SARS-CoV-2 pneumonia
inferred← citeshttps://doi.org/10.1038/s41467-020-18466-wopenalex-snapshot
IL-33-ST2 axis regulates myeloid cell differentiation and activation enabling effective club cell regeneration
inferred← citeshttps://doi.org/10.1038/s41467-021-27428-9openalex-snapshot
Oxidative stress-induced FABP5 S-glutathionylation protects against acute lung injury by suppressing inflammation in macrophages
inferred← citeshttps://doi.org/10.1038/s41467-023-44421-6openalex-snapshot
Alveolar macrophage-expressed Plet1 is a driver of lung epithelial repair after viral pneumonia
inferred← citeshttps://doi.org/10.1038/s41467-024-48589-3openalex-snapshot
Vascular endothelial-derived SPARCL1 exacerbates viral pneumonia through pro-inflammatory macrophage activation
inferred← citeshttps://doi.org/10.1038/s41590-018-0064-8openalex-snapshot
Innate immune responses to trauma
inferred← citeshttps://doi.org/10.1038/s41598-019-38864-5openalex-snapshot
Intranasal and epicutaneous administration of Toll-like receptor 7 (TLR7) agonists provides protection against influenza A virus-induced morbidity in mice
inferred← citeshttps://doi.org/10.1039/d3nr04401gopenalex-snapshot
ICAM-1 targeted and ROS-responsive nanoparticles for the treatment of acute lung injury
inferred← citeshttps://doi.org/10.1042/bj20131510openalex-snapshot
miR-429 regulates alveolar macrophage inflammatory cytokine production and is involved in LPS-induced acute lung injury
inferred← citeshttps://doi.org/10.1042/bsr20192132openalex-snapshot
MiR-124-3p helps to protect against acute respiratory distress syndrome by targeting p65
inferred← citeshttps://doi.org/10.1042/cs20160259openalex-snapshot
Pulmonary immunity to viruses
inferred← citeshttps://doi.org/10.1055/s-0036-1584801openalex-snapshot
Human Influenza Virus Infections
inferred← citeshttps://doi.org/10.1055/s-0038-1669477openalex-snapshot
Macrophagic Stabilin-1 Restored Disruption of Vascular Integrity Caused by Sepsis
inferred← citeshttps://doi.org/10.1073/pnas.1821601116openalex-snapshot
STAT6 induces expression of Gas6 in macrophages to clear apoptotic neutrophils and resolve inflammation
inferred← citeshttps://doi.org/10.1073/pnas.2314747121openalex-snapshot
Precision treatment of viral pneumonia through macrophage-targeted lipid nanoparticle delivery
inferred← citeshttps://doi.org/10.1080/21655979.2022.2047406openalex-snapshot
Suppression of NOD-like receptor protein 3 inflammasome activation and macrophage M1 polarization by hederagenin contributes to attenuation of sepsis-induced acute lung injury in rats
inferred← citeshttps://doi.org/10.1089/ars.2013.5469openalex-snapshot
Lung Injury and Lung Cancer Caused by Cigarette Smoke-Induced Oxidative Stress: Molecular Mechanisms and Therapeutic Opportunities Involving the Ceramide-Generating Machinery and Epidermal Growth Factor Receptor
inferred← citeshttps://doi.org/10.1093/toxsci/kfw226openalex-snapshot
Editor’s Highlight: CCR2 Regulates Inflammatory Cell Accumulation in the Lung and Tissue Injury following Ozone Exposure
inferred← citeshttps://doi.org/10.1093/toxsci/kfy309openalex-snapshot
Role of Macrophages in Acute Lung Injury and Chronic Fibrosis Induced by Pulmonary Toxicants
inferred← citeshttps://doi.org/10.1096/fj.201802259ropenalex-snapshot
The α/β–hydrolase domain 6 inhibitor WWL70 decreases endotoxin‐induced lung inflammation in mice, potential contribution of 2‐arachidonoylglycerol, and lysoglycerophospholipids
inferred← citeshttps://doi.org/10.1096/fj.202301722ropenalex-snapshot
Lactate produced by alveolar type II cells suppresses inflammatory alveolar macrophages in acute lung injury
inferred← citeshttps://doi.org/10.1097/shk.0000000000000820openalex-snapshot
M2A and M2C Macrophage Subsets Ameliorate Inflammation and Fibroproliferation in Acute Lung Injury Through Interleukin 10 Pathway
inferred← citeshttps://doi.org/10.1097/shk.0000000000001601openalex-snapshot
Tissue-Resident Macrophages in the Control of Infection and Resolution of Inflammation
inferred← citeshttps://doi.org/10.1097/shk.0b013e318294f85aopenalex-snapshot
Protein Kinase C and Acute Respiratory Distress Syndrome
inferred← citeshttps://doi.org/10.1097/ta.0000000000004499openalex-snapshot
Lung contusion complicated by pneumonia worsens lung injury via the inflammatory effect of alveolar small extracellular vesicles on macrophages and epithelial cells
inferred← citeshttps://doi.org/10.1101/2021.03.03.433654openalex-snapshot
Pro-inflammatory alveolar macrophages associated with allograft dysfunction after lung transplantation
inferred← citeshttps://doi.org/10.1101/2025.05.16.654442openalex-snapshot
Long-term immune reprogramming of classical monocytes with altered ontogeny mediates enhanced lung injury in sepsis survivors
inferred← citeshttps://doi.org/10.1101/2025.10.16.682758openalex-snapshot
The Janus face of Selinexor (KPT-330) in bacterial infection: short-term protection versus long-term lethality
inferred← citeshttps://doi.org/10.1111/2049-632x.12189openalex-snapshot
Low-dose cisplatin administration to septic mice improves bacterial clearance and programs peritoneal macrophage polarization to M1 phenotype
inferred← citeshttps://doi.org/10.1111/j.1365-2613.2012.00833.xopenalex-snapshot
The role of macrophages in healing the wounded lung
inferred← citeshttps://doi.org/10.1111/jcmm.15481openalex-snapshot
MCTR1 enhances the resolution of lipopolysaccharide‐induced lung injury through STAT6‐mediated resident M2 alveolar macrophage polarization in mice
inferred← citeshttps://doi.org/10.1111/jcmm.15860openalex-snapshot
Mesenchymal stem cell–secreted extracellular vesicles carrying TGF‐β1 up‐regulate miR‐132 and promote mouse M2 macrophage polarization
inferred← citeshttps://doi.org/10.1111/jth.14685openalex-snapshot
Effects of nebulized antithrombin and heparin on inflammatory and coagulation alterations in an acute lung injury model in rats
inferred← citeshttps://doi.org/10.1111/jvim.17169openalex-snapshot
Time to resolution of airway inflammation caused by bronchoalveolar lavage in healthy horses
inferred← citeshttps://doi.org/10.1111/resp.14297openalex-snapshot
Targeting the human β c receptor inhibits inflammatory myeloid cells and lung injury caused by acute cigarette smoke exposure
inferred← citeshttps://doi.org/10.1126/scisignal.abd2533openalex-snapshot
The suppressive effects of Mer inhibition on inflammatory responses in the pathogenesis of LPS-induced ALI/ARDS
inferred← citeshttps://doi.org/10.1136/bmjresp-2023-001762openalex-snapshot
Protective role of the HSP90 inhibitor, STA-9090, in lungs of SARS-CoV-2-infected Syrian golden hamsters
inferred← citeshttps://doi.org/10.1146/annurev-immunol-082323-031852openalex-snapshot
The Interplay Between Innate Immunity and Nonimmune Cells in Lung Damage, Inflammation, and Repair
inferred← citeshttps://doi.org/10.1152/ajplung.00018.2015openalex-snapshot
Sex differences in the expression of lung inflammatory mediators in response to ozone
inferred← citeshttps://doi.org/10.1152/ajplung.00089.2015openalex-snapshot
TRIM72 modulates caveolar endocytosis in repair of lung cells
inferred← citeshttps://doi.org/10.1152/ajplung.00141.2016openalex-snapshot
Selective and inducible targeting of CD11b+mononuclear phagocytes in the murine lung with hCD68-rtTA transgenic systems
inferred← citeshttps://doi.org/10.1152/ajplung.00199.2018openalex-snapshot
Apoptosis signal-regulating kinase-1 promotes inflammasome priming in macrophages
inferred← citeshttps://doi.org/10.1152/ajplung.00232.2013openalex-snapshot
Novel concepts of acute lung injury and alveolar-capillary barrier dysfunction
inferred← citeshttps://doi.org/10.1152/ajplung.00341.2013openalex-snapshot
Diverse macrophage populations mediate acute lung inflammation and resolution
inferred← citeshttps://doi.org/10.1152/ajplung.00419.2015openalex-snapshot
Enhanced resolution of experimental ARDS through IL-4-mediated lung macrophage reprogramming
inferred← citeshttps://doi.org/10.1155/2013/435236openalex-snapshot
The Extent of Ventilator-Induced Lung Injury in Mice Partly Depends on Duration of Mechanical Ventilation
inferred← citeshttps://doi.org/10.1155/2013/457189openalex-snapshot
Hyperoxia Exacerbates Postnatal Inflammation-Induced Lung Injury in Neonatal BRP-39 Null Mutant Mice Promoting the M1 Macrophage Phenotype
inferred← citeshttps://doi.org/10.1155/2013/769214openalex-snapshot
Macrophage Heterogeneity in Respiratory Diseases
inferred← citeshttps://doi.org/10.1155/2014/749097openalex-snapshot
Ibuprofen Protects Ventilator-Induced Lung Injury by Downregulating Rho-Kinase Activity in Rats
inferred← citeshttps://doi.org/10.1155/2016/3735452openalex-snapshot
Mesenchymal Stem Cell-Educated Macrophages Ameliorate LPS-Induced Systemic Response
inferred← citeshttps://doi.org/10.1155/2018/1264913openalex-snapshot
The Role of Macrophages in the Pathogenesis of ALI/ARDS
inferred← citeshttps://doi.org/10.1155/2018/9269154openalex-snapshot
Mechanism of MCP-1 in Acute Lung Injury and Advanced Therapy by Drug-Loaded Dextrin Nanoparticle
inferred← citeshttps://doi.org/10.1155/2021/6666370openalex-snapshot
Mesenchymal Stem Cells and COVID-19: Cure, Prevention, and Vaccination
inferred← citeshttps://doi.org/10.1155/2021/8876484openalex-snapshot
Contribution of Thrombospondin‐1 and ‐2 to Lipopolysaccharide‐Induced Acute Respiratory Distress Syndrome
inferred← citeshttps://doi.org/10.1155/2021/8883962openalex-snapshot
Luteolin Regulates the Differentiation of Regulatory T Cells and Activates IL-10-Dependent Macrophage Polarization against Acute Lung Injury
inferred← citeshttps://doi.org/10.1155/2022/8450673openalex-snapshot
Gu-Ben-Zhi-Ke-Zhong-Yao Alleviated PM2.5-Induced Lung Injury via HMGB1/NF-κB Axis
inferred← citeshttps://doi.org/10.1155/2022/9470845openalex-snapshot
Detection of Radiolabeled Inflammatory Cell Macrophage Subpopulations in Chronic Respiratory Diseases: Results from Preliminary Analyses
inferred← citeshttps://doi.org/10.1155/2024/6631882openalex-snapshot
The Identification Distinct Antiviral Factors Regulated Influenza Pandemic H1N1 Infection
inferred← citeshttps://doi.org/10.1159/000522338openalex-snapshot
Lipidomic Profiling of Bronchoalveolar Lavage Fluid Extracellular Vesicles Indicates Their Involvement in Lipopolysaccharide-Induced Acute Lung Injury
inferred← citeshttps://doi.org/10.1160/th17-05-0347openalex-snapshot
Nebulized Heparin Attenuates Pulmonary Coagulopathy and Inflammation through Alveolar Macrophages in a Rat Model of Acute Lung Injury
inferred← citeshttps://doi.org/10.1165/rcmb.2014-0118ocopenalex-snapshot
Myeloid-Specific Fos-Related Antigen-1 Regulates Cigarette Smoke–Induced Lung Inflammation, Not Emphysema, in Mice
inferred← citeshttps://doi.org/10.1165/rcmb.2022-0089wsopenalex-snapshot
New Insights into Clinical and Mechanistic Heterogeneity of the Acute Respiratory Distress Syndrome: Summary of the Aspen Lung Conference 2021
inferred← citeshttps://doi.org/10.1167/iovs.65.10.22openalex-snapshot
Macrophages Modulate Optic Nerve Crush Injury Scar Formation and Retinal Ganglion Cell Function
inferred← citeshttps://doi.org/10.1172/jci.insight.123158openalex-snapshot
Anti–spike IgG causes severe acute lung injury by skewing macrophage responses during acute SARS-CoV infection
inferred← citeshttps://doi.org/10.1172/jci.insight.124061openalex-snapshot
Integrating molecular pathogenesis and clinical translation in sepsis-induced acute respiratory distress syndrome
inferred← citeshttps://doi.org/10.1172/jci.insight.182700openalex-snapshot
Gpnmb and Spp1 mark a conserved macrophage injury response masking fibrosis-specific programming in the lung
inferred← citeshttps://doi.org/10.1172/jci.insight.185834openalex-snapshot
Effect of aging on pulmonary cellular responses during mechanical ventilation
inferred← citeshttps://doi.org/10.1177/0261192920983015openalex-snapshot
Modulating the Barrier Function of Human Alveolar Epithelial (hAELVi) Cell Monolayers as a Model of Inflammation
inferred← citeshttps://doi.org/10.1177/0960327120926254openalex-snapshot
MicroRNA: Potential biomarker and target of therapy in acute lung injury
inferred← citeshttps://doi.org/10.1177/09636897221124485openalex-snapshot
Identification of Immune Infiltration and Effective Immune Biomarkers in Acute Lung Injury by Bioinformatics Analysis
inferred← citeshttps://doi.org/10.1177/09636897231196489openalex-snapshot
Repairing Mechanisms for Distal Airway Injuries and Related Targeted Therapeutics for Chronic Lung Diseases
inferred← citeshttps://doi.org/10.1177/15353702231157940openalex-snapshot
The inflammatory profiles of pulmonary alveolar macrophages and alveolar type 2 cells in SCD
inferred← citeshttps://doi.org/10.1177/2045893217752660openalex-snapshot
Injured lung endothelium: mechanisms of self‐repair and agonist‐assisted recovery (2017 Grover Conference Series)
inferred← citeshttps://doi.org/10.1183/09031936.00186214openalex-snapshot
Influenza virus-induced lung injury: pathogenesis and implications for treatment
inferred← citeshttps://doi.org/10.1183/16000617.0263-2023openalex-snapshot
The guardians of pulmonary harmony: alveolar macrophages orchestrating the symphony of lung inflammation and tissue homeostasis
inferred← citeshttps://doi.org/10.1186/s12861-015-0082-9openalex-snapshot
Evidence for lung epithelial stem cell niches
inferred← citeshttps://doi.org/10.1186/s12880-015-0059-yopenalex-snapshot
Intrapulmonary administration of bone-marrow derived M1/M2 macrophages to enhance the resolution of LPS-induced lung inflammation: noninvasive monitoring using free-breathing MR and CT imaging protocols
inferred← citeshttps://doi.org/10.1186/s12917-022-03446-7openalex-snapshot
Immune cell composition of the bronchoalveolar lavage fluid in healthy and respiratory diseased dromedary camels
inferred← citeshttps://doi.org/10.1186/s12931-018-0937-2openalex-snapshot
Lipoxin A4 receptor agonist BML-111 induces autophagy in alveolar macrophages and protects from acute lung injury by activating MAPK signaling
inferred← citeshttps://doi.org/10.1186/s12931-026-03627-0openalex-snapshot
Telomere damage-mediated senescence in alveolar epithelial type II cells but not in macrophages aggravates inflammation in acute lung injury
inferred← citeshttps://doi.org/10.1186/s12951-016-0164-2openalex-snapshot
An in vitro alveolar macrophage assay for predicting the short-term inhalation toxicity of nanomaterials
inferred← citeshttps://doi.org/10.1186/s12951-020-00593-7openalex-snapshot
Manipulation of macrophage polarization by peptide-coated gold nanoparticles and its protective effects on acute lung injury
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