Cited by 99Neuroinflammation and Neurodegeneration MechanismsNeurogenesis and neuroplasticity mechanismsMultiple Sclerosis Research Studies

A limited capacity for microglial repopulation in the adult brain

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Najafi, Allison R., Crapser, Joshua, Jiang, Shan, Ng, Winnie, Mortazavi, Ali, West, Brian L., Green, Kim N.·2018·Glia

Abstract

Microglia are the resident immune cell of the central nervous system (CNS), and serve to protect and maintain the local brain environment. Microglia are critically dependent on signaling through the colony‐stimulating factor 1 receptor (CSF1R); administration of CSF1R inhibitors that cross the blood brain barrier (BBB) lead to the elimination of up to 99% of microglia, depending on CNS exposure and treatment duration. Once microglia are depleted, withdrawal of inhibitor stimulates repopulation of the entire CNS with new cells, conceivably enabling a therapeutic strategy for beneficial renewal of the entire microglial tissue. We have explored the kinetics and limits of this repopulation event and show that the rate of microglial repopulation is proportional to the extent of microglial depletion – greater depletion of microglia results in more rapid repopulation. Using a CSF1R inhibitor formulation that eliminates approximately 99% of microglia within 7 days, we subjected mice to multiple rounds of elimination (7 days’ treatment) and repopulation (7 days’ recovery) and found that the brain only has the capacity for a single complete repopulation event; subsequent elimination and CSF1R inhibitor withdrawal fail to repopulate the brain. However, if the recovery time between, or after, cycles is extended sufficiently then the brain can ultimately repopulate. These kinetic studies define the opportunities and possible limits of the remarkable renewal capacities of microglia.

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References 49 · Cited by 99

Authors
Najafi, A. R., Crapser, J., Jiang, S., Ng, W., Mortazavi, A., West, B. L., & Green, K. N.
Affiliations
  • University of California, Irvine (US)
  • Plexxikon (United States) (US)
Corresponding author
Green, Kim N.
Venue
Glia
Publisher
Wiley
Published
2018-10-28
Volume
66
Issue
11
Pages
2385-2396
ISSN
  • 0894-1491 (ISSN-L)
  • 1098-1136
OpenAlex
W2899174889
Cited by
99
References
49
Citations by year
2026: 7 · 2025: 20 · 2024: 8 · 2023: 13 · 2022: 11 · 2021: 17 · 2020: 15 · 2019: 8
FWCI
4.49
Type
journal article
Language
en
Open access
Locations
  • Glia (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
  • eScholarship (California Digital Library) (submittedVersion)
Funders
National Institutes of Health (AG00096, AG016573, P50, R01NS083801)
Topics
  • Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
  • Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
  • Health Sciences › Medicine › Pathology and Forensic Medicine › Multiple Sclerosis Research Studies
Keywords
microglia, microglial repopulation, CSF1R inhibition, colony-stimulating factor 1 receptor, microglial depletion, blood-brain barrier, microglial homeostasis
MeSH terms
CX3C Chemokine Receptor 1, Aminopyridines, Animals, Brain, Calcium-Binding Proteins, Dose-Response Relationship, Drug, Glial Fibrillary Acidic Protein, Luminescent Proteins, Male, Mice, Inbred C57BL, Mice, Transgenic, Microfilament Proteins, Pyrroles, Signal Transduction, Receptors, Granulocyte-Macrophage Colony-Stimulating Factor, Cytokines, Microglia, Receptor, Platelet-Derived Growth Factor alpha, Gene Expression Profiling, Mice, Gene Ontology

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