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. Microglia respond to environmental challenges, such as signals from the gut microbiome, in a sex- and time-dependent manner.
Journal article
Microbiome Influences Prenatal and Adult Microglia in a Sex-Specific Manner
Cell, Vol.172(3), pp.500-516.e16
25/Jan/2018
PMID: 29275859
Published (Version of record)CC BY V4.0, Open Access
Abstract
Details
- Title
- Microbiome Influences Prenatal and Adult Microglia in a Sex-Specific Manner
- Creators
- Morgane Sonia Thion (null) - Université Paris Sciences et LettresDonovan Low (null) - Agency for Science, Technology and ResearchAymeric Silvin (null) - Agency for Science, Technology and ResearchJinmiao Chen (null) - Agency for Science, Technology and ResearchPauline Grisel (null) - Université Paris Sciences et LettresJonas Schulte-Schrepping (null) - University of BonnRonnie Blecher (null) - 972WIS_INST___120Thomas Ulas (null) - University of BonnPaola Squarzoni (null) - Université Paris Sciences et LettresGuillaume Hoeffel (null) - Centre d’Immunologie de Marseille-LuminyFanny Coulpier (null) - Université Paris Sciences et LettresEleni Siopi (null) - Institut PasteurFriederike Sophie David (null) - University of BonnClaus Scholz (null) - University of BonnFoo Shihui (null) - Agency for Science, Technology and ResearchJosephine Lum (null) - Agency for Science, Technology and ResearchArlaine Anne Amoyo (null) - National Cancer Centre SingaporeAnis Larbi (null) - Agency for Science, Technology and ResearchMichael Poidinger (null) - Agency for Science, Technology and ResearchAnne Buttgereit (null) - University of ZurichPierre-Marie Lledo (null) - Institut PasteurMelanie Greter (null) - University of ZurichJerry Kok Yen Chan (null) - KK Women's and Children's HospitalIdo Amit (null) - 972WIS_INST___120Marc Beyer (null) - German Center for Neurodegenerative DiseasesJoachim Ludwig Schultze (null) - German Center for Neurodegenerative DiseasesAndreas Schlitzer (null) - Agency for Science, Technology and ResearchSven Pettersson (null) - Karolinska InstitutetFlorent Ginhoux (Corresponding Author) - Agency for Science, Technology and ResearchSonia Garel (null) - Université Paris Sciences et Lettres
- Resource Type
- Journal article
- Publication Details
- Cell, Vol.172(3), pp.500-516.e16; 25/Jan/2018
- Language
- English
- DOI
- https://doi.org/10.1016/j.cell.2017.11.042
- PMID
- 29275859
- Grant note
- We are grateful to the Garel and Ginhoux lab for discussions and critical comments on the manuscript. We thank Lucy Robinson for editing the manuscript, Esther Klingler and Samuel Collombet for scientific discussions, the IBENS Imaging Facility (France BioImaging, supported by ANR-10-INBS-04, ANR-10-LABX-54 MEMO LIFE and ANR-11-IDEX-000-02 PSL∗ Reseach University, “Investments for the future”), the cytometry core facility of Institut Curie for cell sorting, the IBENS transcriptomic facility (by the France Génomique national infrastructure, funded as part of the “Investissements d’Avenir” program [contract ANR-10-INBS-09]). We are grateful to C. Auger, A. Delecourt, E. Touzalin, D. Valera and C. Le Moal for excellent technical assistance. This work was supported by grants from the LKC School of Medicine, SCELSE, MOE (Tier1 grant), NIMBLE grant NTU, NTU GUTME grant, Swedish Medical Council (VR to S.P.), the DFG (SFB704 to J.L.S., M.B., and T.U. and SCHL 2116/1-1 to A.S.), the Federal Ministry for Economic Affairs and Energy (BMWi Project FASTGENOMICS to J.L.S.), the European Union’s Horizon 2020 (733100-SYSCID to M.B., J.S.S., and J.L.S.), INSERM, CNRS, the ERC Consolidator (NImO 616080 to S.G.), and from the Merlion Program (to S.G and F.G.). M.B., A.S., and J.L.S. are members of the Excellence Cluster ImmunoSensation. F.G. and S.G. are EMBO YIP awardees.
- Record Identifier
- 993264001503596
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