TY - JOUR
T1 - Transient microglial absence assists postmigratory cortical neurons in proper differentiation
AU - Hattori, Yuki
AU - Naito, Yu
AU - Tsugawa, Yoji
AU - Nonaka, Shigenori
AU - Wake, Hiroaki
AU - Nagasawa, Takashi
AU - Kawaguchi, Ayano
AU - Miyata, Takaki
N1 - Funding Information:
We thank Makoto Masaoka and Namiko Noguchi (Department of Anatomy and Cell Biology, Graduate School of Medicine, Nagoya University) for technical assistance. We are grateful to Carina Hanashima (Department of Biology, Faculty of Education and Integrated Arts and Sciences, Waseda University) and Koji Oishi (Department of Anatomy, Keio University School of Medicine) for helpful advice and suggestion. This work was supported by JSPS KAKENHI Grant numbers JP16H02457 [T.M.], JP16K15169 [T.M.], JP16J06207 (Grant-in-Aid for JSPS Fellows) [Y.H.] and JP18K15003 (Grant-in-Aid for Young Scientists) [Y.H.], and by a grant from the Uehara Memorial Fundation (Grant number 201910147) to Y.H. The two-photon imaging in this study was supported by NIBB Collaborative Research Program for Integrative Imaging (16-504) to T.M.
Publisher Copyright:
© 2020, The Author(s).
PY - 2020/12/1
Y1 - 2020/12/1
N2 - In the developing cortex, postmigratory neurons accumulate in the cortical plate (CP) to properly differentiate consolidating subtype identities. Microglia, despite their extensive surveying activity, temporarily disappear from the midembryonic CP. However, the mechanism and significance of this absence are unknown. Here, we show that microglia bidirectionally migrate via attraction by CXCL12 released from the meninges and subventricular zone and thereby exit the midembryonic CP. Upon nonphysiological excessive exposure to microglia in vivo or in vitro, young postmigratory and in vitro-grown CP neurons showed abnormal differentiation with disturbed expression of the subtype-associated transcription factors and genes implicated in functional neuronal maturation. Notably, this effect is primarily attributed to interleukin 6 and type I interferon secreted by microglia. These results suggest that “sanctuarization” from microglia in the midembryonic CP is required for neurons to appropriately fine-tune the expression of molecules needed for proper differentiation, thus securing the establishment of functional cortical circuit.
AB - In the developing cortex, postmigratory neurons accumulate in the cortical plate (CP) to properly differentiate consolidating subtype identities. Microglia, despite their extensive surveying activity, temporarily disappear from the midembryonic CP. However, the mechanism and significance of this absence are unknown. Here, we show that microglia bidirectionally migrate via attraction by CXCL12 released from the meninges and subventricular zone and thereby exit the midembryonic CP. Upon nonphysiological excessive exposure to microglia in vivo or in vitro, young postmigratory and in vitro-grown CP neurons showed abnormal differentiation with disturbed expression of the subtype-associated transcription factors and genes implicated in functional neuronal maturation. Notably, this effect is primarily attributed to interleukin 6 and type I interferon secreted by microglia. These results suggest that “sanctuarization” from microglia in the midembryonic CP is required for neurons to appropriately fine-tune the expression of molecules needed for proper differentiation, thus securing the establishment of functional cortical circuit.
UR - http://www.scopus.com/inward/record.url?scp=85082920933&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85082920933&partnerID=8YFLogxK
U2 - 10.1038/s41467-020-15409-3
DO - 10.1038/s41467-020-15409-3
M3 - Article
C2 - 32242005
AN - SCOPUS:85082920933
SN - 2041-1723
VL - 11
JO - Nature communications
JF - Nature communications
IS - 1
M1 - 1631
ER -