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Mammalian musculoskeletal regeneration is associated with reduced inflammatory cytokines and an influx of T cells

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What this work says

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

inferredcites →https://doi.org/10.1002/dvdy.10239openalex-snapshot

Regeneration or scarring: An immunologic perspective

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Global analysis of gene expression in Xenopus hindlimbs during stage‐dependent complete and incomplete regeneration

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Comparative and developmental study of the immune system in Xenopus

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Dedifferentiation and the role of sall4 in reprogramming and patterning during amphibian limb regeneration

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Rapid induction and clearance of TGFβ1 is an early response to wounding in the mouse embryo

inferredcites →https://doi.org/10.1002/jez.1402220212openalex-snapshot

Cyclophosphamide‐induced leukopenia and suppression of limb regeneration in the adult newt, Notophthalmus viridescens

inferredcites →https://doi.org/10.1002/jmor.20155openalex-snapshot

Skin wound healing in different aged Xenopus laevis

inferredcites →https://doi.org/10.1002/reg2.50openalex-snapshot

Ear wound regeneration in the African spiny mouse Acomys cahirinus

inferredcites →https://doi.org/10.1002/reg2.77openalex-snapshot

Macrophages and fibroblasts during inflammation and tissue repair in models of organ regeneration

inferredcites →https://doi.org/10.1002/sctm.17-0213openalex-snapshot

Concise Review: Translating Regenerative Biology into Clinically Relevant Therapies: Are We on the Right Path?

inferredcites →https://doi.org/10.1007/bf00848570openalex-snapshot

Limb regeneration of the adult newt (Notophthalmus viridescens) in the absence of the spleen

inferredcites →https://doi.org/10.1016/0022-4804(82)90110-xopenalex-snapshot

Thymic inhibition of wound healing: Abrogation by adult thymectomy

inferredcites →https://doi.org/10.1016/0022-4804(83)90112-9openalex-snapshot

Cyclosporine a impairs wound healing in rats

inferredcites →https://doi.org/10.1016/b978-0-12-369439-3.x5000-4openalex-snapshot

Principles of Regenerative Biology

inferredcites →https://doi.org/10.1016/b978-0-12-800180-6.00004-9openalex-snapshot

New Insights into Vertebrate Skin Regeneration

inferredcites →https://doi.org/10.1016/j.actbio.2017.01.056openalex-snapshot

Promoting tissue regeneration by modulating the immune system

inferredcites →https://doi.org/10.1016/j.ajpath.2013.02.032openalex-snapshot

Macrophages Are Essential for the Early Wound Healing Response and the Formation of a Fibrovascular Scar

inferredcites →https://doi.org/10.1016/j.celrep.2016.07.041openalex-snapshot

STAT3 Regulates Self-Renewal of Adult Muscle Satellite Cells during Injury-Induced Muscle Regeneration

inferredcites →https://doi.org/10.1016/j.dci.2016.02.015openalex-snapshot

Inflammation and immunity in organ regeneration

inferredcites →https://doi.org/10.1016/j.devcel.2017.11.010openalex-snapshot

Zebrafish Regulatory T Cells Mediate Organ-Specific Regenerative Programs

inferredcites →https://doi.org/10.1016/j.diff.2014.02.002openalex-snapshot

Scar-free wound healing and regeneration in amphibians: Immunological influences on regenerative success

inferredcites →https://doi.org/10.1016/j.exer.2009.07.012openalex-snapshot

Reactive oxygen species (ROS) are essential mediators in epidermal growth factor (EGF)-stimulated corneal epithelial cell proliferation, adhesion, migration, and wound healing

inferredcites →https://doi.org/10.1016/j.jdermsci.2009.09.005openalex-snapshot

Scarless healing of oral mucosa is characterized by faster resolution of inflammation and control of myofibroblast action compared to skin wounds in the red Duroc pig model

inferredcites →https://doi.org/10.1016/j.jss.2014.12.026openalex-snapshot

Celecoxib inhibits early cutaneous wound healing

inferredcites →https://doi.org/10.1016/j.lfs.2016.04.017openalex-snapshot

Selective inhibition of COX-2 improves cutaneous wound healing of pressure ulcers in mice through reduction of iNOS expression

inferredcites →https://doi.org/10.1016/j.mcn.2013.06.005openalex-snapshot

STAT3 integrates cytokine and neurotrophin signals to promote sympathetic axon regeneration

inferredcites →https://doi.org/10.1016/j.tcb.2005.09.002openalex-snapshot

Inflammatory cells during wound repair: the good, the bad and the ugly

inferredcites →https://doi.org/10.1016/j.ydbio.2017.08.007openalex-snapshot

The blastema and epimorphic regeneration in mammals

inferredcites →https://doi.org/10.1016/s0002-9440(10)61717-8openalex-snapshot

Wound Healing in MIP-1α−/− and MCP-1−/− Mice

inferredcites →https://doi.org/10.1016/s0012-1606(05)80018-1openalex-snapshot

Immunohistochemical localization of growth factors in fetal wound healing

inferredcites →https://doi.org/10.1016/s0022-2143(96)90023-2openalex-snapshot

Cyclooxygenase 2 induction: Molecular mechanism and pathophysiologic roles

inferredcites →https://doi.org/10.1016/s0167-5699(05)80005-2openalex-snapshot

The involvement of TNF, IL-1 and IL-6 in the immune response to protozoan parasites

inferredcites →https://doi.org/10.1016/s0891-5849(03)00318-6openalex-snapshot

T cell receptor-stimulated generation of hydrogen peroxide inhibits MEK-ERK activation and lck serine phosphorylation

inferredcites →https://doi.org/10.1016/s1074-7613(03)00296-6openalex-snapshot

The IL-12 Family of Heterodimeric Cytokines

inferredcites →https://doi.org/10.1021/jm960803qopenalex-snapshot

Synthesis and Biological Evaluation of the 1,5-Diarylpyrazole Class of Cyclooxygenase-2 Inhibitors: Identification of 4-[5-(4-Methylphenyl)-3- (trifluoromethyl)-1 H -pyrazol-1-yl]benzenesulfonamide (SC-58635, Celecoxib)

inferredcites →https://doi.org/10.1038/jid.2011.245openalex-snapshot

Autocrine Regulation of Re-Epithelialization After Wounding by Chemokine Receptors CCR1, CCR10, CXCR1, CXCR2, and CXCR3

inferredcites →https://doi.org/10.1038/nature11499openalex-snapshot

Skin shedding and tissue regeneration in African spiny mice (Acomys)

inferredcites →https://doi.org/10.1038/nature17655openalex-snapshot

Normalizing the environment recapitulates adult human immune traits in laboratory mice

inferredcites →https://doi.org/10.1038/ncb2659openalex-snapshot

Amputation-induced reactive oxygen species are required for successful Xenopus tadpole tail regeneration

inferredcites →https://doi.org/10.1038/ncomms11164openalex-snapshot

Comparative analysis of ear-hole closure identifies epimorphic regeneration as a discrete trait in mammals

inferredcites →https://doi.org/10.1038/ncomms14811openalex-snapshot

The comparative immunology of wild and laboratory mice, Mus musculus domesticus

inferredcites →https://doi.org/10.1038/ncomms3633openalex-snapshot

Cross-talk between KLF4 and STAT3 regulates axon regeneration

inferredcites →https://doi.org/10.1038/ni1117-1271bopenalex-snapshot

Erratum: Corrigendum: IL-6 as a keystone cytokine in health and disease

inferredcites →https://doi.org/10.1038/s41536-017-0027-yopenalex-snapshot

Heart regeneration in the salamander relies on macrophage-mediated control of fibroblast activation and the extracellular landscape

inferredcites →https://doi.org/10.1038/s41598-017-09334-7openalex-snapshot

De novo transcriptome assembly for the spiny mouse (Acomys cahirinus)

inferredcites →https://doi.org/10.1038/srep02084openalex-snapshot

Sustained production of ROS triggers compensatory proliferation and is required for regeneration to proceed

inferredcites →https://doi.org/10.1042/bj3340297openalex-snapshot

Interleukin-6-type cytokine signalling through the gp130/Jak/STAT pathway

inferredcites →https://doi.org/10.1046/j.1523-1747.2000.00034.xopenalex-snapshot

Delayed Wound Healing in CXCR2 Knockout Mice

inferredcites →https://doi.org/10.1046/j.1524-475x.2003.11106.xopenalex-snapshot

Reduction of scar formation in full‐thickness wounds with topical celecoxib treatment

inferredcites →https://doi.org/10.1073/pnas.1012016107openalex-snapshot

Induction of regulatory T cells by macrophages is dependent on production of reactive oxygen species

inferredcites →https://doi.org/10.1073/pnas.1300290110openalex-snapshot

Macrophages are required for adult salamander limb regeneration

inferredcites →https://doi.org/10.1073/pnas.1800618115openalex-snapshot

T reg cells limit IFN-γ production to control macrophage accrual and phenotype during skeletal muscle regeneration

inferredcites →https://doi.org/10.1084/jem.187.4.601openalex-snapshot

Abnormalities in Monocyte Recruitment and Cytokine Expression in Monocyte Chemoattractant Protein 1–deficient Mice

inferredcites →https://doi.org/10.1089/jir.2008.0027openalex-snapshot

Monocyte Chemoattractant Protein-1 (MCP-1): An Overview

inferredcites →https://doi.org/10.1093/bib/bbx108openalex-snapshot

MAFFT online service: multiple sequence alignment, interactive sequence choice and visualization

inferredcites →https://doi.org/10.1093/intimm/dxw006openalex-snapshot

CD4 + T-cell subsets in inflammatory diseases: beyond the T h 1/T h 2 paradigm

inferredcites →https://doi.org/10.1093/nar/gkf436openalex-snapshot

MAFFT: a novel method for rapid multiple sequence alignment based on fast Fourier transform

inferredcites →https://doi.org/10.1096/fj.00-0073comopenalex-snapshot

Impaired cutaneous wound healing in interleukin‐6‐deficient and immunosuppressed mice

inferredcites →https://doi.org/10.1096/fj.08-117721openalex-snapshot

Signal transducer and activator of transcription 3 is a transcriptional factor regulating the gene expression of SALL4

inferredcites →https://doi.org/10.1097/00000658-198904000-00015openalex-snapshot

The Effect of In Vivo T Helper and T Suppressor Lymphocyte Depletion on Wound Healing

inferredcites →https://doi.org/10.1101/cshperspect.a016295openalex-snapshot

IL-6 in Inflammation, Immunity, and Disease

inferredcites →https://doi.org/10.1111/j.1365-3016.2008.00969.xopenalex-snapshot

Assays with lower detection limits: implications for epidemiological investigations

inferredcites →https://doi.org/10.1111/j.1440-1711.2006.01440.xopenalex-snapshot

Increased IL‐4 production and attenuated proliferative and pro‐inflammatory responses of splenocytes from wild‐caught rats (Rattus norvegicus)

inferredcites →https://doi.org/10.1111/j.1469-7580.2006.00626.xopenalex-snapshot

Regeneration, tissue injury and the immune response

inferredcites →https://doi.org/10.1111/wrr.12385openalex-snapshot

Cellular events during scar‐free skin regeneration in the spiny mouse, Acomys

inferredcites →https://doi.org/10.1126/science.276.5309.75openalex-snapshot

Wound Healing--Aiming for Perfect Skin Regeneration

inferredcites →https://doi.org/10.1126/science.aam7928openalex-snapshot

Inflammation and metabolism in tissue repair and regeneration

inferredcites →https://doi.org/10.1126/scitranslmed.3004754openalex-snapshot

Terminally Differentiated CD8 + T Cells Negatively Affect Bone Regeneration in Humans

inferredcites →https://doi.org/10.1128/jcm.32.10.2441-2447.1994openalex-snapshot

Determination of parallelism and nonparallelism in bioassay dilution curves

inferredcites →https://doi.org/10.1146/annurev.immunol.25.022106.141557openalex-snapshot

IL-17 Family Cytokines and the Expanding Diversity of Effector T Cell Lineages

inferredcites →https://doi.org/10.1172/jci72181openalex-snapshot

Macrophages are required for neonatal heart regeneration

inferredcites →https://doi.org/10.1177/154405910308200810openalex-snapshot

Differential Injury Responses in Oral Mucosal and Cutaneous Wounds

inferredcites →https://doi.org/10.1186/1471-2164-11-471openalex-snapshot

Positional differences in the wound transcriptome of skin and oral mucosa

inferredcites →https://doi.org/10.1186/s12859-017-1934-zopenalex-snapshot

ImageJ2: ImageJ for the next generation of scientific image data

inferredcites →https://doi.org/10.1189/jlb.0212072openalex-snapshot

Trauma equals danger—damage control by the immune system

inferredcites →https://doi.org/10.1189/jlb.0802397openalex-snapshot

Essential involvement of IL-6 in the skin wound-healing process as evidenced by delayed wound healing in IL-6-deficient mice

inferredcites →https://doi.org/10.1242/dev.098459openalex-snapshot

Macrophages modulate adult zebrafish tail fin regeneration

inferredcites →https://doi.org/10.1242/dev.142034openalex-snapshot

Early bioelectric activities mediate redox-modulated regeneration

inferredcites →https://doi.org/10.1242/dev.150086openalex-snapshot

Macrophages are required to coordinate mouse digit tip regeneration

inferredcites →https://doi.org/10.1242/jcs.107.5.1159openalex-snapshot

Macrophage recruitment during limb development and wound healing in the embryonic and foetal mouse

inferredcites →https://doi.org/10.1371/journal.pone.0079804openalex-snapshot

Central Role for MCP-1/CCL2 in Injury-Induced Inflammation Revealed by In Vitro, In Silico, and Clinical Studies

inferredcites →https://doi.org/10.1371/journal.pone.0080477openalex-snapshot

Changes in the Inflammatory Response to Injury and Its Resolution during the Loss of Regenerative Capacity in Developing Xenopus Limbs

inferredcites →https://doi.org/10.1371/journal.pone.0091146openalex-snapshot

Reactive Oxygen Species Prevent Imiquimod-Induced Psoriatic Dermatitis through Enhancing Regulatory T Cell Function

inferredcites →https://doi.org/10.2353/ajpath.2006.060010openalex-snapshot

Kupffer Cells and Their Mediators

inferredcites →https://doi.org/10.2353/ajpath.2009.081002openalex-snapshot

A Transgenic Mouse Model of Inducible Macrophage Depletion

inferredcites →https://doi.org/10.2353/ajpath.2009.090248openalex-snapshot

Selective and Specific Macrophage Ablation Is Detrimental to Wound Healing in Mice

inferredcites →https://doi.org/10.3389/fimmu.2017.01481openalex-snapshot

The Immunology of Wild Rodents: Current Status and Future Prospects

inferredcites →https://doi.org/10.4049/jimmunol.0901929openalex-snapshot

Differences in Wound Healing in Mice with Deficiency of IL-6 versus IL-6 Receptor

inferredcites →https://doi.org/10.4049/jimmunol.0903356openalex-snapshot

Differential Roles of Macrophages in Diverse Phases of Skin Repair

inferredcites →https://doi.org/10.4049/jimmunol.1302821openalex-snapshot

CCL2 Shapes Macrophage Polarization by GM-CSF and M-CSF: Identification of CCL2/CCR2-Dependent Gene Expression Profile

inferredcites →https://doi.org/10.4049/jimmunol.1303486openalex-snapshot

CD8 T Cells Are Involved in Skeletal Muscle Regeneration through Facilitating MCP-1 Secretion and Gr1high Macrophage Infiltration

inferredcites →https://doi.org/10.4049/jimmunol.1502139openalex-snapshot

Cutting Edge: Regulatory T Cells Facilitate Cutaneous Wound Healing

inferredcites →https://doi.org/10.4155/bio-2017-0084openalex-snapshot

Parallelism Experiments to Evaluate Matrix Effects, Selectivity and Sensitivity in Ligand-Binding Assay Method Development: Pros and Cons

inferredcites →https://doi.org/10.7554/elife.24623openalex-snapshot

Macrophages are necessary for epimorphic regeneration in African spiny mice

What points at this work

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

inferred← citeshttps://doi.org/10.1016/j.gde.2020.05.019openalex-snapshot

Regeneration in the spiny mouse, Acomys, a new mammalian model

inferred← citeshttps://doi.org/10.1016/j.regen.2019.100026openalex-snapshot

Healing power: The mammalian macrophage in skeletal regeneration, scar formation, and regenerative medicine

inferred← citeshttps://doi.org/10.1101/pdb.top100966openalex-snapshot

Xenopus , a Model to Study Wound Healing and Regeneration: Experimental Approaches

inferred← citeshttps://doi.org/10.1242/dev.167718openalex-snapshot

Model systems for regeneration: the spiny mouse, Acomys cahirinus

inferred← citeshttps://doi.org/10.1371/journal.pone.0241617openalex-snapshot

Spiny mice (Acomys) exhibit attenuated hallmarks of aging and rapid cell turnover after UV exposure in the skin epidermis

inferred← citeshttps://doi.org/10.17760/d20383670openalex-snapshot

Tissue repair and stress responses of aged skin epidermis

inferred← citeshttps://doi.org/10.3389/fimmu.2020.01695openalex-snapshot

Complex Tissue Regeneration in Mammals Is Associated With Reduced Inflammatory Cytokines and an Influx of T Cells

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