MiR-137-3p rescue motoneuron death by targeting calpain-2

被引:18
|
作者
Tang, Ying [1 ,2 ]
Fu, Rao [1 ,2 ]
Ling, Ze-Min [1 ,2 ]
Liu, Lin-lin [1 ,2 ]
Yu, Guang-yin [1 ,2 ]
Li, Wen [3 ]
Fang, Xin-yu [3 ]
Zhu, Zhe [3 ]
Wu, Wu-tian [3 ,4 ,5 ]
Zhou, Li-Hua [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Zhongshan Sch Med, Dept Anat, 74 Zhongshan Rd 2, Guangzhou 510080, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Zhongshan Sch Med, Guangdong Prov Key Lab Brain Funct & Dis, 74 Zhongshan Rd 2, Guangzhou 510080, Guangdong, Peoples R China
[3] Univ Hong Kong, LKS Fac Med, Sch Biomed Sci, Pokfulam 999077, Hong Kong, Peoples R China
[4] Jinan Univ, Guangdong Hongkong Macau Inst CNS Regenerat GHMIC, Guangzhou 510632, Guangdong, Peoples R China
[5] Univ Hong Kong, State Key Lab Brain & Cognit Sci, Pokfulam 999077, Hong Kong, Peoples R China
来源
基金
美国国家科学基金会;
关键词
miR-137-3p; Calpain-2; nNOS; Neuron death; Brachial plexus root avulsion; NITRIC-OXIDE SYNTHASE; SPINAL-CORD-INJURY; CENTRAL-NERVOUS-SYSTEM; ROOT-AVULSION; MOTOR-NEURONS; ADULT-RAT; ALZHEIMERS-DISEASE; STEM-CELLS; C-JUN; EXPRESSION;
D O I
10.1016/j.niox.2018.01.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Brachial plexus root avulsion (BPRA) is a type of injury that leads to motor function loss as a result of moto-neurons (MNs) degeneration. Here we identified that the reduced expression of rat miR-137-3p in the ventral horn of spinal cord was associated with MNs death. However, the pathophysiological role of miR-137-3p in root avulsion remains poorly understood. We demonstrated that the calcium-activated neutral protease-2 (calpain-2) was a direct target gene of miR-137-3p with miR-137-3p binding to the 3'-untranslated region of calpain-2. Silencing of calpain-2 suppressed the expression of neuronal nitric oxide synthase (nNOS), a primary source of nitric oxide (NO). After avulsion 2 weeks, up-regulation of miR-137-3p in the spinal cord reduced calpain-2 levels and nNOS expression inside spinal MNs, resulting in an amelioration of the MNs death. These events provide new insight into the mechanism by which upregulation of miR-137-3p can impair MN survival in the BPRA.
引用
收藏
页码:74 / 85
页数:12
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