Protein post-translational modifications after spinal cord injury

被引:5
|
作者
Zhu, Shuang [1 ]
Yang, Bing-Sheng [1 ]
Li, Si-Jing [1 ]
Tong, Ge [2 ]
Tan, Jian-Ye [1 ]
Wu, Guo-Feng [1 ]
Li, Lin [1 ]
Chen, Guo-Li [3 ]
Chen, Qian [4 ]
Lin, Li-Jun [1 ]
机构
[1] Southern Med Univ, Zhujiang Hosp, Dept Joint & Orthoped, Guangzhou, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Dept Med Ultrason, Guangdong Prov Key Lab Hepatol Res, Affiliated Hosp 3, Guangzhou, Guangdong, Peoples R China
[3] Putian Univ, Dept Orthoped, Affiliated Hosp, Putian, Fujian, Peoples R China
[4] Brown Univ, Rhode Isl Hosp, Alpert Med Sch, Cell & Mol Biol Lab,Dept Orthopaed, Providence, RI 02903 USA
基金
中国国家自然科学基金;
关键词
extracellular matrix; function impairment; glial scar; nerve regeneration; neuropathic pain; post-translational modification; spinal cord injury; therapeutic target;
D O I
10.4103/1673-5374.308068
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Deficits in intrinsic neuronal capacities in the spinal cord, a lack of growth support, and suppression of axonal outgrowth by inhibitory molecules mean that spinal cord injury almost always has devastating consequences. As such, one of the primary targets for the treatment of spinal cord injury is to develop strategies to antagonize extrinsic or intrinsic axonal growth-inhibitory factors or enhance the factors that support axonal growth. Among these factors, a series of individual protein level disorders have been identified during the generation of axons following spinal cord injury. Moreover, an increasing number of studies have indicated that post-translational modifications of these proteins have important implications for axonal growth. Some researchers have discovered a variety of post-translational modifications after spinal cord injury, such as tyrosination, acetylation, and phosphorylation. In this review, we reviewed the post-translational modifications for axonal growth, functional recovery, and neuropathic pain after spinal cord injury, a better understanding of which may elucidate the dynamic change of spinal cord injury-related molecules and facilitate the development of a new therapeutic strategy for spinal cord injury.
引用
收藏
页码:1935 / 1943
页数:9
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