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

Morgane Sonia Thion(Centre National de la Recherche Scientifique), Donovan Low(Agency for Science, Technology and Research), Aymeric Silvin(Agency for Science, Technology and Research), Jinmiao Chen(Agency for Science, Technology and Research), Pauline Grisel(Centre National de la Recherche Scientifique), Jonas Schulte-Schrepping(University of Bonn), Ronnie Blecher‐Gonen(Weizmann Institute of Science), Thomas Ulas(University of Bonn), Paola Squarzoni(Centre National de la Recherche Scientifique), Guillaume Hoeffel(Agency for Science, Technology and Research), Fanny Coulpier(Centre National de la Recherche Scientifique), Eleni Siopi(Centre National de la Recherche Scientifique), Friederike S. David(University of Bonn), Claus Jürgen Scholz(University of Bonn), Foo Shihui(Agency for Science, Technology and Research), Josephine Lum(Agency for Science, Technology and Research), Arlaine Anne Amoyo(National Cancer Centre Singapore), Anis Larbi(Agency for Science, Technology and Research), Michael Poidinger(Agency for Science, Technology and Research), Anne Buttgereit(University of Zurich), Pierre-Marie Lledo(Centre National de la Recherche Scientifique), Melanie Greter(University of Zurich), Jerry Kok Yen Chan(KK Women's and Children's Hospital), Ido Amit(Weizmann Institute of Science), Marc Beyer(University of Bonn), Joachim L. Schultze(University of Bonn), Andreas Schlitzer(Agency for Science, Technology and Research), Sven Pettersson(Nanyang Technological University), Florent Ginhoux(Agency for Science, Technology and Research), Sonia Garel(Centre National de la Recherche Scientifique)
Cell
December 21, 2017
Cited by 761Open Access
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Abstract

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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