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Protein post-translational modifications after spinal cord injury. | LitMetric

Protein post-translational modifications after spinal cord injury.

Neural Regen Res

Department of Joint and Orthopedics, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong Province, China.

Published: October 2021

AI Article Synopsis

  • * A primary focus for treatment is to counteract these growth-inhibitory factors or enhance the supportive factors that promote axonal growth.
  • * Research has identified various post-translational modifications (such as tyrosination, acetylation, and phosphorylation) of proteins that are crucial for axonal growth and recovery after spinal cord injury, potentially leading to new therapeutic strategies.

Article Abstract

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.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8343325PMC
http://dx.doi.org/10.4103/1673-5374.308068DOI Listing

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