Schwann cell‐specific RhoA knockout accelerates peripheral nerve regeneration via promoting Schwann cell dedifferentiation

Author:

Liu Jingmin12,Ma Xinrui1,Hu Xiaofang1,Wen Jinkun1,Zhang Haowen1,Xu Jiawei1,He Ye1,Wang Xianghai134,Guo Jiasong134ORCID

Affiliation:

1. Department of Histology and Embryology, Guangdong Provincial Key Laboratory of Construction and Detection in Tissue Engineering, School of Basic Medical Sciences Southern Medical University Guangzhou 510515 China

2. Department of Spine Orthopedics, Nanfang Hospital Southern Medical University Guangzhou 510515 China

3. Key Laboratory of Mental Health of the Ministry of Education, Guangdong‐Hong Kong‐Macao Greater Bay Area Center for Brain Science and Brain‐Inspired Intelligence Guangdong Province Key Laboratory of Psychiatric Disorders Guangzhou 510515 China

4. National Experimental Education Demonstration Center for Basic Medical Sciences, National Virtual & Reality Experimental Education Center for Medical Morphology, School of Basic Medical Sciences Southern Medical University Guangzhou 510515 China

Abstract

AbstractOur previous studies indicated that RhoA knockdown or inhibition could alleviate the proliferation, migration, and differentiation of Schwann cells. However, the role of RhoA in Schwann cells during nerve injury and repair is still unknown. Herein, we developed two lines of Schwann cells conditional RhoA knockout (cKO) mice by breeding RhoAflox/flox mice with PlpCre‐ERT2 or DhhCre mice. Our results indicate that RhoA cKO in Schwann cells accelerates axonal regrowth and remyelination after sciatic nerve injury, which enhances the recovery of nerve conduction and hindlimb gait, and alleviates the amyotrophy in gastrocnemius muscle. Mechanistic studies in both in vivo and in vitro models revealed that RhoA cKO could facilitate Schwann cell dedifferentiation via JNK pathway. Schwann cell dedifferentiation subsequently promotes Wallerian degeneration by enhancing phagocytosis and myelinophagy, as well as stimulating the production of neurotrophins (NT‐3, NGF, BDNF, and GDNF). These findings shed light on the role of RhoA in Schwann cells during nerve injury and repair, indicating that cell type‐specific RhoA targeting could serve as a promising molecular therapeutic strategy for peripheral nerve injury.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Neurology

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