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Specific microRNAs for Modulation of Autophagy in Spinal Cord Injury
被引:0
|作者:
Visintin, Rhett
[1
]
Ray, Swapan K.
[2
]
机构:
[1] Univ South Carolina, Dept Chem & Biochem, Columbia, SC 29208 USA
[2] Univ South Carolina, Sch Med, Dept Pathol Microbiol & Immunol, Columbia, SC 29209 USA
基金:
美国国家卫生研究院;
关键词:
spinal cord injury (SCI);
autophagy;
neurodegeneration;
miRNAs;
miRNAs for modulation of autophagy;
neuroprotection;
functional recovery;
ISCHEMIA-REPERFUSION INJURY;
TRAUMATIC BRAIN-INJURY;
CONTACT SITES;
ENDOPLASMIC-RETICULUM;
MACROPHAGE AUTOPHAGY;
NEURONAL AUTOPHAGY;
APOPTOSIS;
MTORC1;
CELLS;
AMPK;
D O I:
10.3390/brainsci12020247
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
The treatment of spinal cord injury (SCI) is currently a major challenge, with a severe lack of effective therapies for yielding meaningful improvements in function. Therefore, there is a great opportunity for the development of novel treatment strategies for SCI. The modulation of autophagy, a process by which a cell degrades and recycles unnecessary or harmful components (protein aggregates, organelles, etc.) to maintain cellular homeostasis and respond to a changing microenvironment, is thought to have potential for treating many neurodegenerative conditions, including SCI. The discovery of microRNAs (miRNAs), which are short ribonucleotide transcripts for targeting of specific messenger RNAs (mRNAs) for silencing, shows prevention of the translation of mRNAs to the corresponding proteins affecting various cellular processes, including autophagy. The number of known miRNAs and their targets continues to grow rapidly. This review article aims to explore the relationship between autophagy and SCI, specifically with the intent of identifying specific miRNAs that can be useful to modulate autophagy for neuroprotection and the improvement of functional recovery in SCI.
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页数:21
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