SCG10 is required for peripheral axon maintenance and regeneration in mice

Author:

Li Yuanjun1,Tian Yonglu23ORCID,Pei Xiayuhe1,Zheng Pengli14ORCID,Miao Linqing5,Li Lingjun6,Luo Chunxiong6,Zhang Peixun7,Jiang Baoguo7ORCID,Teng Junlin1ORCID,Huang Ning89ORCID,Chen Jianguo16ORCID

Affiliation:

1. College of Life Sciences, Peking University 1 Ministry of Education Key Laboratory of Cell Proliferation and Differentiation , , Beijing 100871 , China

2. School of Psychological and Cognitive Sciences, Peking University 2 , Beijing 100871 , China

3. IDG/McGovern Institute for Brain Research, Peking University 3 , Beijing 100871 , China

4. Peking-Tsinghua Center for Life Sciences, Academy for Advanced Interdisciplinary Studies, Peking University 4 , Beijing 100871 , China

5. Beijing Advanced Innovation Center for Intelligent Robots and Systems, Beijing Institute of Technology 5 , Beijing 100081 , China

6. Center for Quantitative Biology, Peking University 6 , Beijing 100871 , China

7. Peking University People's Hospital 7 , Beijing 100044 , China

8. Institute of Neuroscience, Translational Medicine Institute, Health Science Center, Xi'an Jiaotong University 8 , Xi'an 710061 , China

9. School of Basic Medical Sciences, Health Science Center, Xi'an Jiaotong University 9 Department of Physiology and Pathophysiology , , Xi'an 710061 , China

Abstract

ABSTRACT Proper microtubule dynamics are critical for neuronal morphogenesis and functions, and their dysregulation results in neurological disorders and regeneration failure. Superior cervical ganglion-10 (SCG10, also known as stathmin-2 or STMN2) is a well-known regulator of microtubule dynamics in neurons, but its functions in the peripheral nervous system remain largely unknown. Here, we show that Scg10 knockout mice exhibit severely progressive motor and sensory dysfunctions with significant sciatic nerve myelination deficits and neuromuscular degeneration. Additionally, increased microtubule stability, shown by a significant increase in tubulin acetylation and decrease in tubulin tyrosination, and decreased axonal transport were observed in Scg10 knockout dorsal root ganglion (DRG) neurons. Furthermore, SCG10 depletion impaired axon regeneration in both injured mouse sciatic nerve and cultured DRG neurons following replating, and the impaired axon regeneration was found to be induced by a lack of SCG10-mediated microtubule dynamics in the neurons. Thus, our results highlight the importance of SCG10 in peripheral axon maintenance and regeneration.

Funder

Major State Basic Research Development Program of China

Beijing Municipal Natural Science Foundation

National Key Research and Development Program of China

China Postdoctoral Science Foundation

Publisher

The Company of Biologists

Subject

Cell Biology

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