TY - JOUR
T1 - Microbiome Influences Prenatal and Adult Microglia in a Sex-Specific Manner
AU - Thion, Morgane Sonia
AU - Low, Donovan
AU - Silvin, Aymeric
AU - Chen, Jinmiao
AU - Grisel, Pauline
AU - Schulte-Schrepping, Jonas
AU - Blecher, Ronnie
AU - Ulas, Thomas
AU - Squarzoni, Paola
AU - Hoeffel, Guillaume
AU - Coulpier, Fanny
AU - Siopi, Eleni
AU - David, Friederike Sophie
AU - Scholz, Claus
AU - Shihui, Foo
AU - Lum, Josephine
AU - Amoyo, Arlaine Anne
AU - Larbi, Anis
AU - Poidinger, Michael
AU - Buttgereit, Anne
AU - Lledo, Pierre Marie
AU - Greter, Melanie
AU - Chan, Jerry Kok Yen
AU - Amit, Ido
AU - Beyer, Marc
AU - Schultze, Joachim Ludwig
AU - Schlitzer, Andreas
AU - Pettersson, Sven
AU - Ginhoux, Florent
AU - Garel, Sonia
N1 - Publisher Copyright:
© 2017 The Authors
PY - 2018/1/25
Y1 - 2018/1/25
N2 - 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.
AB - 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.
KW - CXCR4
KW - antibiotics
KW - embryogenesis
KW - germ-free
KW - microbiome
KW - microglia
KW - neurodevelopmental disorders
KW - neuroinflammation
KW - prenatal
KW - sex
UR - http://www.scopus.com/inward/record.url?scp=85038884468&partnerID=8YFLogxK
U2 - 10.1016/j.cell.2017.11.042
DO - 10.1016/j.cell.2017.11.042
M3 - Article
C2 - 29275859
AN - SCOPUS:85038884468
SN - 0092-8674
VL - 172
SP - 500-516.e16
JO - Cell
JF - Cell
IS - 3
ER -