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Microglia limit lesion expansion and promote functional recovery after spinal cord injury in mice

https://doi.org/10.1101/410258
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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/(sici)1096-9861(19970120)377:3<443::aid-cne10>3.0.co;2-sopenalex-snapshot
Cellular inflammatory response after spinal cord injury in sprague-dawley and lewis rats
inferredcites →https://doi.org/10.1002/ana.22421openalex-snapshot
The blood–spinal cord barrier: Morphology and Clinical Implications
inferredcites →https://doi.org/10.1002/ana.410270107openalex-snapshot
Inhibition of mononuclear phagocytes reduces ischemic injury in the spinal cord
inferredcites →https://doi.org/10.1002/cne.10736openalex-snapshot
Rats and mice exhibit distinct inflammatory reactions after spinal cord injury
inferredcites →https://doi.org/10.1002/cne.20827openalex-snapshot
Comparative analysis of lesion development and intraspinal inflammation in four strains of mice following spinal contusion injury
inferredcites →https://doi.org/10.1002/cne.22282openalex-snapshot
Regional heterogeneity in astrocyte responses following contusive spinal cord injury in mice
inferredcites →https://doi.org/10.1002/glia.22774openalex-snapshot
Macrophages in spinal cord injury: Phenotypic and functional change from exposure to myelin debris
inferredcites →https://doi.org/10.1006/exnr.1999.7118openalex-snapshot
Depletion of Hematogenous Macrophages Promotes Partial Hindlimb Recovery and Neuroanatomical Repair after Experimental Spinal Cord Injury
inferredcites →https://doi.org/10.1006/exnr.2002.7959openalex-snapshot
Both Dorsal and Ventral Spinal Cord Pathways Contribute to Overground Locomotion in the Adult Rat
inferredcites →https://doi.org/10.1016/0166-2236(96)10049-7openalex-snapshot
Microglia: a sensor for pathological events in the CNS
inferredcites →https://doi.org/10.1016/0306-4522(90)90229-wopenalex-snapshot
Heterogeneity in the distribution and morphology of microglia in the normal adult mouse brain
inferredcites →https://doi.org/10.1016/0306-4522(94)90220-8openalex-snapshot
Effects of silica on the outcome from experimental spinal cord injury: Implication of macrophages in secondary tissue damage
inferredcites →https://doi.org/10.1016/j.bbr.2006.11.042openalex-snapshot
Adaptation of a ladder beam walking task to assess locomotor recovery in mice following spinal cord injury
inferredcites →https://doi.org/10.1016/j.cmet.2017.05.015openalex-snapshot
Microglial Inflammatory Signaling Orchestrates the Hypothalamic Immune Response to Dietary Excess and Mediates Obesity Susceptibility
inferredcites →https://doi.org/10.1016/j.expneurol.2007.06.009openalex-snapshot
Inflammation and its role in neuroprotection, axonal regeneration and functional recovery after spinal cord injury
inferredcites →https://doi.org/10.1016/j.expneurol.2008.04.024openalex-snapshot
α4β1 integrin blockade after spinal cord injury decreases damage and improves neurological function
inferredcites →https://doi.org/10.1016/j.expneurol.2010.03.010openalex-snapshot
A combination immunomodulatory treatment promotes neuroprotection and locomotor recovery after contusion SCI
inferredcites →https://doi.org/10.1016/j.expneurol.2013.05.002openalex-snapshot
Mobilisation of the splenic monocyte reservoir and peripheral CX3CR1 deficiency adversely affects recovery from spinal cord injury
inferredcites →https://doi.org/10.1016/j.immuni.2013.02.012openalex-snapshot
Recruitment of Beneficial M2 Macrophages to Injured Spinal Cord Is Orchestrated by Remote Brain Choroid Plexus
inferredcites →https://doi.org/10.1016/j.nbd.2014.10.024openalex-snapshot
Hematogenous macrophage depletion reduces the fibrotic scar and increases axonal growth after spinal cord injury
inferredcites →https://doi.org/10.1016/j.neuroimage.2012.11.048openalex-snapshot
Vertebral landmarks for the identification of spinal cord segments in the mouse
inferredcites →https://doi.org/10.1016/j.neuron.2014.02.040openalex-snapshot
Colony-Stimulating Factor 1 Receptor Signaling Is Necessary for Microglia Viability, Unmasking a Microglia Progenitor Cell in the Adult Brain
inferredcites →https://doi.org/10.1016/j.neuron.2014.07.027openalex-snapshot
TNF and Increased Intracellular Iron Alter Macrophage Polarization to a Detrimental M1 Phenotype in the Injured Spinal Cord
inferredcites →https://doi.org/10.1016/s0165-3806(99)00113-3openalex-snapshot
Microglia derive from progenitors, originating from the yolk sac, and which proliferate in the brain
inferredcites →https://doi.org/10.1038/nature21029openalex-snapshot
Neurotoxic reactive astrocytes are induced by activated microglia
inferredcites →https://doi.org/10.1038/nn.3318openalex-snapshot
Microglia emerge from erythromyeloid precursors via Pu.1- and Irf8-dependent pathways
inferredcites →https://doi.org/10.1038/nn.3599openalex-snapshot
Identification of a unique TGF-β–dependent molecular and functional signature in microglia
inferredcites →https://doi.org/10.1038/nprot.2012.119openalex-snapshot
Three-dimensional imaging of solvent-cleared organs using 3DISCO
inferredcites →https://doi.org/10.1038/srep31545openalex-snapshot
Elimination of microglia improves cognitive function following cranial irradiation
inferredcites →https://doi.org/10.1073/pnas.1525528113openalex-snapshot
New tools for studying microglia in the mouse and human CNS
inferredcites →https://doi.org/10.1089/08977150360547099openalex-snapshot
Experimental Modeling of Spinal Cord Injury: Characterization of a Force-Defined Injury Device
inferredcites →https://doi.org/10.1089/neu.2006.23.635openalex-snapshot
Basso Mouse Scale for Locomotion Detects Differences in Recovery after Spinal Cord Injury in Five Common Mouse Strains
inferredcites →https://doi.org/10.1089/neu.2007.0426openalex-snapshot
A Graded Forceps Crush Spinal Cord Injury Model in Mice
inferredcites →https://doi.org/10.1089/neu.2011.1860openalex-snapshot
Prevention of Both Neutrophil and Monocyte Recruitment Promotes Recovery after Spinal Cord Injury
inferredcites →https://doi.org/10.1089/neu.2011.1976openalex-snapshot
CD11d Antibody Treatment Improves Recovery in Spinal Cord-Injured Mice
inferredcites →https://doi.org/10.1093/brain/awl296openalex-snapshot
The cellular inflammatory response in human spinal cords after injury
inferredcites →https://doi.org/10.1093/brain/awp322openalex-snapshot
Quantitative analysis of cellular inflammation after traumatic spinal cord injury: evidence for a multiphasic inflammatory response in the acute to chronic environment
inferredcites →https://doi.org/10.1093/jnen/60.7.676openalex-snapshot
Bone Marrow Chimeric Rats Reveal the Unique Distribution of Resident and Recruited Macrophages in the Contused Rat Spinal Cord
inferredcites →https://doi.org/10.1097/nen.0b013e3182479b41openalex-snapshot
Differential Detection and Distribution of Microglial and Hematogenous Macrophage Populations in the Injured Spinal Cord oflys-EGFP-kiTransgenic Mice
inferredcites →https://doi.org/10.1097/wco.0000000000000550openalex-snapshot
Emerging targets for reprograming the immune response to promote repair and recovery of function after spinal cord injury
inferredcites →https://doi.org/10.1126/science.1194637openalex-snapshot
Fate Mapping Analysis Reveals That Adult Microglia Derive from Primitive Macrophages
inferredcites →https://doi.org/10.1152/physrev.00011.2010openalex-snapshot
Physiology of Microglia
inferredcites →https://doi.org/10.1172/jci.insight.91229openalex-snapshot
Microglia mediate postoperative hippocampal inflammation and cognitive decline in mice
inferredcites →https://doi.org/10.1182/blood-2002-02-0569openalex-snapshot
A macrophage colony-stimulating factor receptor–green fluorescent protein transgene is expressed throughout the mononuclear phagocyte system of the mouse
inferredcites →https://doi.org/10.1186/s12974-015-0366-9openalex-snapshot
Colony-stimulating factor 1 receptor inhibition prevents microglial plaque association and improves cognition in 3xTg-AD mice
inferredcites →https://doi.org/10.1189/jlb.0303114openalex-snapshot
Microglia, macrophages, perivascular macrophages, and pericytes: a review of function and identification
inferredcites →https://doi.org/10.1371/journal.pmed.1000113openalex-snapshot
Infiltrating Blood-Derived Macrophages Are Vital Cells Playing an Anti-inflammatory Role in Recovery from Spinal Cord Injury in Mice
inferredcites →https://doi.org/10.1371/journal.pone.0122912openalex-snapshot
Characterizing Newly Repopulated Microglia in the Adult Mouse: Impacts on Animal Behavior, Cell Morphology, and Neuroinflammation
inferredcites →https://doi.org/10.1523/jneurosci.0337-15.2015openalex-snapshot
Toll-Like Receptors and Dectin-1, a C-Type Lectin Receptor, Trigger Divergent Functions in CNS Macrophages
inferredcites →https://doi.org/10.1523/jneurosci.0498-17.2017openalex-snapshot
Insights into the Dual Role of Inflammation after Spinal Cord Injury
inferredcites →https://doi.org/10.1523/jneurosci.0584-17.2017openalex-snapshot
Microglia Are Irrelevant for Neuronal Degeneration and Axon Regeneration after Acute Injury
inferredcites →https://doi.org/10.1523/jneurosci.1709-08.2008openalex-snapshot
STAT3 is a Critical Regulator of Astrogliosis and Scar Formation after Spinal Cord Injury
inferredcites →https://doi.org/10.1523/jneurosci.21-10-03392.2001openalex-snapshot
Proliferation of NG2-Positive Cells and Altered Oligodendrocyte Numbers in the Contused Rat Spinal Cord
inferredcites →https://doi.org/10.1523/jneurosci.2121-13.2013openalex-snapshot
Glial Scar Borders Are Formed by Newly Proliferated, Elongated Astrocytes That Interact to Corral Inflammatory and Fibrotic Cells via STAT3-Dependent Mechanisms after Spinal Cord Injury
inferredcites →https://doi.org/10.1523/jneurosci.22-01-00315.2002openalex-snapshot
Functional Redundancy of Ventral Spinal Locomotor Pathways
inferredcites →https://doi.org/10.1523/jneurosci.2751-16.2017openalex-snapshot
Macrophage Transcriptional Profile Identifies Lipid Catabolic Pathways That Can Be Therapeutically Targeted after Spinal Cord Injury
inferredcites →https://doi.org/10.1523/jneurosci.3257-09.2009openalex-snapshot
Identification of Two Distinct Macrophage Subsets with Divergent Effects Causing either Neurotoxicity or Regeneration in the Injured Mouse Spinal Cord
inferredcites →https://doi.org/10.1523/jneurosci.3547-03.2004openalex-snapshot
Reactive Astrocytes Protect Tissue and Preserve Function after Spinal Cord Injury
inferredcites →https://doi.org/10.1523/jneurosci.3953-16.2017openalex-snapshot
Proliferating NG2-Cell-Dependent Angiogenesis and Scar Formation Alter Axon Growth and Functional Recovery After Spinal Cord Injury in Mice
inferredcites →https://doi.org/10.1523/jneurosci.3992-08.2009openalex-snapshot
Macrophages Promote Axon Regeneration with Concurrent Neurotoxicity
inferredcites →https://doi.org/10.1523/jneurosci.5218-14.2015openalex-snapshot
The Complement Receptor C5aR Controls Acute Inflammation and Astrogliosis following Spinal Cord Injury
inferredcites →https://doi.org/10.1523/jneurosci.5343-03.2004openalex-snapshot
Transient Blockade of the CD11d/CD18 Integrin Reduces Secondary Damage after Spinal Cord Injury, Improving Sensory, Autonomic, and Motor Function

What points at this work

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

inferred← citeshttps://doi.org/10.1002/adma.202307747openalex-snapshot
Synergistic Pharmacological Therapy to Modulate Glial Cells in Spinal Cord Injury
inferred← citeshttps://doi.org/10.1002/adma.75202openalex-snapshot
Biomaterial‐Based Controlled Release Systems for Spinal Cord Remyelination
inferred← citeshttps://doi.org/10.1002/glia.70030openalex-snapshot
Microglial IKKβ Alters Central and Peripheral Immune Activity at Distinct Time Points After Spinal Cord Injury
inferred← citeshttps://doi.org/10.1016/j.jphs.2020.07.004openalex-snapshot
Microglia as therapeutic target in central nervous system disorders
inferred← citeshttps://doi.org/10.1016/j.neulet.2019.134370openalex-snapshot
Role of microglia in spinal cord injury
inferred← citeshttps://doi.org/10.1038/s41467-022-31797-0openalex-snapshot
Microglia coordinate cellular interactions during spinal cord repair in mice
inferred← citeshttps://doi.org/10.1038/s41593-020-0597-7openalex-snapshot
Microglia and macrophages promote corralling, wound compaction and recovery after spinal cord injury via Plexin-B2
inferred← citeshttps://doi.org/10.1080/02713683.2019.1669664openalex-snapshot
Neuroinflammation and Optic Nerve Regeneration: Where Do We Stand in Elucidating Underlying Cellular and Molecular Players?
inferred← citeshttps://doi.org/10.1101/2024.07.09.602797openalex-snapshot
Engineering Microglial Cells to Promote Spinal Cord Injury Recovery
inferred← citeshttps://doi.org/10.14245/ns.2244616.308openalex-snapshot
Surgical Considerations to Improve Recovery in Acute Spinal Cord Injury
inferred← citeshttps://doi.org/10.3389/fneur.2021.796704openalex-snapshot
Current Knowledge of Microglia in Traumatic Spinal Cord Injury
inferred← citeshttps://doi.org/10.3390/biomedicines10071673openalex-snapshot
Biomaterial-Mediated Factor Delivery for Spinal Cord Injury Treatment
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