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lncRNA GPRC5D-AS1 通过调控 miR-520d-5p 抑制骨骼肌衰老。

lncRNA GPRC5D-AS1 as a ceRNA inhibits skeletal muscle aging by regulating miR-520d-5p.

机构信息

Department of Geriatrics and Special Medical Treatment, The First Hospital of Jilin University, Changchun 130021, China.

出版信息

Aging (Albany NY). 2023 Dec 9;15(23):13980-13997. doi: 10.18632/aging.205279.

Abstract

Sarcopenia induced by muscle aging is associated with negative outcomes in a variety of diseases. Long non-coding RNAs are a class of RNAs longer than 200 nucleotides with lower protein coding potential. An increasing number of studies have shown that lncRNAs play a vital role in skeletal muscle development. According to our previous research, lncRNA GPRC5D-AS1 is selected in the present study as the target gene to further study its effect on skeletal muscle aging in a dexamethasone-induced human muscle atrophy cell model. As a result, GPRC5D-AS1 functions as a ceRNA of miR-520d-5p to repress cell apoptosis and regulate the expression of muscle regulatory factors, including MyoD, MyoG, Mef2c and Myf5, thus accelerating myoblast proliferation and differentiation, facilitating development of skeletal muscle. In conclusion, lncRNA GPRC5D-AS1 could be a novel therapeutic target for treating sarcopenia.

摘要

肌肉衰老引起的肌肉减少症与多种疾病的不良结局有关。长非编码 RNA 是一类长度大于 200 个核苷酸、蛋白编码潜能较低的 RNA。越来越多的研究表明,lncRNA 在骨骼肌发育中发挥着重要作用。根据我们之前的研究,在本研究中选择 lncRNA GPRC5D-AS1 作为靶基因,进一步研究其在地塞米松诱导的人肌肉萎缩细胞模型中对骨骼肌衰老的影响。结果表明,GPRC5D-AS1 作为 miR-520d-5p 的 ceRNA,抑制细胞凋亡,调节肌肉调节因子的表达,包括 MyoD、MyoG、Mef2c 和 Myf5,从而加速成肌细胞增殖和分化,促进骨骼肌发育。总之,lncRNA GPRC5D-AS1 可能成为治疗肌肉减少症的新的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b85c/10756129/8631ce67659e/aging-15-205279-g001.jpg

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