Cited by 1,180Neuroinflammation and Neurodegeneration MechanismsNeurogenesis and neuroplasticity mechanismsSingle-cell and spatial transcriptomics

Microglia development follows a stepwise program to regulate brain homeostasis

Matcovitch-Natan, Orit, Winter, Deborah R., Giladi, Amir, Vargas Aguilar, Stephanie, Spinrad, Amit, Sarrazin, Sandrine, Ben-Yehuda, Hila, David, Eyal +16 more·2016·Science

Abstract

Microglia development follows a stepwise program: Microglia are cells that defend the central nervous system. However, because they migrate into the brain during development, the changes that they undergo, including those that affect gene expression, have been difficult to document. Matcovitch-Natan et al. transcriptionally profiled gene expression and analyzed epigenetic signatures of microglia at the single-cell level in the early postnatal life of mice. They identified three stages of microglia development, which are characterized by gene expression and linked with chromatin changes, occurring in sync with the developing brain. Furthermore, they showed that the proper development of microglia is affected by the microbiome. Science , this issue p. 789

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Crossref · 10.1126/science.aad8670

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82 of 82 references verified0 citation errors · 0 not checkable

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  • Microglial cells have distinct gene expression profiles during embryonic, early post-natal, and adult stages.

    “Gene expression studies have shown that microglial cells have distinct profiles during the embryonic, early post-natal, and adult stages (26).”
  • MAFB plays a key role in the final stages of microglial development from yolk sac progenitors, supporting the acquisition and maintenance of microglial identity.

    “MAFB is known to play a key role in the final stages of microglial development from yolk sac progenitors, supporting the acquisition and maintenance of microglial identity (19).”
  • MAFB promotes the final stages of microglial development from yolk sac progenitors, facilitating the acquisition and maintenance of microglia identity.

    “Additionally, it promotes the final stages of microglial development from yolk sac progenitors, facilitating the acquisition and maintenance of microglia identity (19).”
  • Intersecting developmentally determined and environment-dependent transcriptional networks establish microglia identity and function.

    “Integration of these findings with recent studies of yolk sac and embryonic microglia (56, 63) suggests a model by which intersecting developmentally determined and environment-dependent transcriptional networks establish microglia identity and function (Fig. 6E).”
  • Mcm5 is an established regulator of microglial cell cycle that is strongly expressed during embryonic and early postnatal microglial development.

    “Mcm5, an established regulator of microglial cell cycle that is strongly expressed during embryonic and early postnatal microglial development”

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Authors
Matcovitch-Natan, O., Winter, D. R., Giladi, A., Vargas Aguilar, S., Spinrad, A., Sarrazin, S., Ben-Yehuda, H., David, E., Zelada González, F., Perrin, P., Keren-Shaul, H., Gury, M., Lara-Astaiso, D., Thaiss, C. A., Cohen, M., Bahar Halpern, K., Baruch, K., Deczkowska, A., Lorenzo-Vivas, E., Itzkovitz, S., Elinav, E., Sieweke, M. H., Schwartz, M., & Amit, I.
Affiliations
  • Weizmann Institute of Science (IL)
  • Centre d'Immunologie de Marseille-Luminy (CIML), Université Aix-Marseille, UM2, Campus de Luminy, Marseille, France.
  • Centre National de la Recherche Scientifique (FR)
  • Department of Immunology, Weizmann Institute of Science, Rehovot, Israel.
  • Department of Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Corresponding author
  • Matcovitch-Natan, Orit
  • Winter, Deborah R.
  • Sieweke, Michael H.
  • Schwartz, Michal
  • Amit, Ido
Venue
Science
Published
2016-08-19
Volume
353
Issue
6301
Pages
aad8670-aad8670
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2468501494
Cited by
1,180
References
82
Citations by year
2026: 76 · 2025: 111 · 2024: 119 · 2023: 105 · 2022: 144 · 2021: 145 · 2020: 143 · 2019: 117 · 2018: 119 · 2017: 84 · 2016: 17
FWCI
61.54
Type
journal article
Language
en
Open access
closed
Locations
  • Science (publishedVersion)
  • PubMed (publishedVersion)
  • HAL (submittedVersion)
  • MDC Repository (Max-Delbrueck-Center for Molecular Medicine) (submittedVersion)
Funders
  • European Research Council (309788)
  • Israeli Science Foundation (1782/11)
  • European Commission Seventh Framework Programme (EC FP7)
  • Ernest and Bonnie Beutler Research Program of Excellence in Genomic Medicine
  • Minerva Stiftung
  • Israeli Ministry of Science, Technology and Space
  • David and Fela Shapell Family Foundation
  • National Human Genome Research Institute Center for Excellence in Genome Science (1P50HG006193)
  • Alan and Laraine Fischer Career Development Chair
  • Advanced European Research Council (232835)
  • EC FP7 HEALTH-2011 (279017)
  • Agence Nationale de la Recherche (ANR BLAN07-1_205752, ANR-11-BSV3-026-01)
  • Fondation pour la Recherche Medicale (20071210559, 20110421320)
  • InCA (13-10/405/AB-LC-HS)
Topics
  • Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
  • Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Single-cell and spatial transcriptomics
Keywords
microglia development, brain homeostasis, MAFB, chromatin regulation, single-cell transcriptomics, microbiome, prenatal immune activation, neurodevelopmental disorders, immune pathways, myeloid cells
MeSH terms
Animals, Blood-Brain Barrier, Brain, Chromatin, Female, Homeostasis, Immunity, Mice, Inbred C57BL, Microglia, Mice, Knockout, Gene Expression Profiling, Myeloid Cells, Histone Code, Epigenesis, Genetic, MafB Transcription Factor, Mice, Neurogenesis, Gene Knockout Techniques, Single-Cell Analysis

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