4.8 Article

Microbiome Influences Prenatal and Adult Microglia in a Sex-Specific Manner

Journal

CELL
Volume 172, Issue 3, Pages 500-+

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2017.11.042

Keywords

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Funding

  1. PSL* Reseach University, Investments for the future [ANR-10-INBS-04, ANR-10-LABX-54 MEMO LIFE, ANR-11-IDEX-000-02]
  2. Investissements d'Avenir'' program [ANR-10-INBS-09]
  3. LKC School of Medicine
  4. SCELSE
  5. MOE (Tier1 grant)
  6. NIMBLE grant NTU
  7. NTU GUTME grant
  8. Swedish Medical Council (VR)
  9. DFG [SFB704, SCHL 2116/1-1]
  10. Federal Ministry for Economic Affairs and Energy (BMWi Project FASTGENOMICS)
  11. European Union's Horizon 2020 [733100-SYSCID]
  12. INSERM
  13. CNRS
  14. ERC Consolidator [NImO 616080]
  15. Merlion Program
  16. EMBO YIP

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Microglia are embryonically seeded macrophages that contribute to brain development, homeostasis, and pathologies. It is thus essential to decipher how microglial properties are temporally regulated by intrinsic and extrinsic factors, such as sexual identity and the microbiome. Here, we found that microglia undergo differentiation phases, discernable by transcriptomic signatures and chromatin accessibility landscapes, which can diverge in adult males and females. Remarkably, the absence of microbiome in germ-free mice had a time and sexually dimorphic impact both prenatally and postnatally: microglia were more profoundly perturbed in male embryos and female adults. Antibiotic treatment of adult mice triggered sexually biased microglial responses revealing both acute and long-term effects of microbiota depletion. Finally, human fetal microglia exhibited significant overlap with the murine transcriptomic signature. Our study shows that microglia respond to environmental challenges in a sex- and time-dependent manner from prenatal stages, with major implications for our understanding of microglial contributions to health and disease.

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