ERK signaling expands mammalian cortical radial glial cells and extends the neurogenic period

Author:

Sun Mengge1ORCID,Gao Yanjing1,Li Zhenmeiyu1,Yang Lin1,Liu Guoping1ORCID,Xu Zhejun1ORCID,Guo Rongliang1ORCID,You Yan1,Yang Zhengang1ORCID

Affiliation:

1. State Key Laboratory of Medical Neurobiology and Ministry of Education Frontiers Center for Brain Science, Institutes of Brain Science, and Department of Neurology, Zhongshan Hospital, Fudan University, Shanghai 200032, China

Abstract

The molecular basis for cortical expansion during evolution remains largely unknown. Here, we report that fibroblast growth factor (FGF)-extracellular signal-regulated kinase (ERK) signaling promotes the self-renewal and expansion of cortical radial glial (RG) cells. Furthermore, FGF-ERK signaling induces bone morphogenic protein 7 ( Bmp7 ) expression in cortical RG cells, which increases the length of the neurogenic period. We demonstrate that ERK signaling and Sonic Hedgehog (SHH) signaling mutually inhibit each other in cortical RG cells. We provide evidence that ERK signaling is elevated in cortical RG cells during development and evolution. We propose that the expansion of the mammalian cortex, notably in human, is driven by the ERK-BMP7-GLI3R signaling pathway in cortical RG cells, which participates in a positive feedback loop through antagonizing SHH signaling. We also propose that the relatively short cortical neurogenic period in mice is partly due to mouse cortical RG cells receiving higher SHH signaling that antagonizes ERK signaling.

Funder

Ministry of Science and Technology of the People's Republic of China

MOST | National Natural Science Foundation of China

Science and Technology Commission of Shanghai Municipality

Publisher

Proceedings of the National Academy of Sciences

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1. The Principle of Cortical Development and Evolution;Neuroscience Bulletin;2024-07-18

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