Lateral/caudal ganglionic eminence makes limited contribution to cortical oligodendrocytes

Author:

Li Jialin1,Yang Feihong2,Tian Yu1,Wang Ziwu1,Qi Dashi3,Yang Zhengang1ORCID,Song Jiangang2,Ding Jing1,Wang Xin1,Zhang Zhuangzhi1ORCID

Affiliation:

1. State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Institutes of Brain Science, and Department of Neurology, Zhongshan Hospital, Fudan University

2. Department of Anesthesiology, Shuguang Hospital Affiliated with Shanghai University of Traditional Chinese Medicine

3. Center for Clinical Research and Translational Medicine, Yangpu Hospital, School of Medicine, Tongji University

Abstract

The emergence of myelinating oligodendrocytes represents a pivotal developmental milestone in vertebrates, given their capacity to ensheath axons and facilitate the swift conduction of action potentials. It is widely accepted that cortical oligodendrocyte progenitor cells (OPCs) arise from medial ganglionic eminence (MGE), lateral/caudal ganglionic eminence (LGE/CGE), and cortical radial glial cells (RGCs). Here, we used two different fate mapping strategies to challenge the established notion that the LGE generates cortical OPCs. Furthermore, we used a Cre/loxP-dependent exclusion strategy to reveal that the LGE/CGE does not give rise to cortical OPCs. Additionally, we showed that specifically eliminating MGE-derived OPCs leads to a significant reduction of cortical OPCs. Together, our findings indicate that the LGE does not generate cortical OPCs, contrary to previous beliefs. These findings provide a new view of the developmental origins of cortical OPCs and a valuable foundation for future research on both normal development and oligodendrocyte-related disease.

Funder

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

National Natural Science Foundation of China

Science and Technology Commission of Shanghai Municipality

Shanghai Municipal Science and Technology Major Project

Publisher

eLife Sciences Publications, Ltd

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