LncRNA BC083743 Promotes the Proliferation of Schwann Cells and Axon Regeneration Through miR-103-3p/BDNF After Sciatic Nerve Crush. Issue 10 (28th June 2020)

• Record Type: Journal Article
• Authors: Gao, Lin; Feng, Aiqin; Yue, Peijian; Liu, Yue; Zhou, Qiaoyu; Zang, Qiuling; Teng, Junfang
• Is Part Of: Journal of neuropathology and experimental neurology. Volume 79:Issue 10(2020)
• Page Start: 1100
• Page End: 1114
• Publication Date: 2020-06-28
• Subjects: BC083743 -- Brain-derived neurotrophic factor -- miR-103-3p -- Sciatic nerve crush -- Schwann cells; Neurology -- Diseases -- Periodicals; Neurology -- Diseases -- Physiopathology -- Periodicals; 616.8047
• DOI: 10.1093/jnen/nlaa069
• Languages: English
• ISSNs: 0022-3069

Abstract

Abstract: To investigate the underlying mechanism of lncRNA BC083743 in regulating the proliferation of Schwann cells (SCs) and axon regeneration after sciatic nerve crush (SNC), we used a rat model. Sciatic function index and the atrophy ratio of gastrocnemius muscle were evaluated. The relationship among BC083743, miR-103-3p, and brain-derived neurotrophic factor (BDNF) and their regulation mechanism in the repair of SNC were investigated using in vivo and in vitro experiments. The expression changes of BC083743 were positively associated with that of BDNF following SNC, but the expression changes of miR-103-3p were inversely associated with that of BDNF. The SC proliferation and BDNF expression could be promoted by overexpression of BC083743, while they were inhibited by a miR-103-3p mimic. In addition, BC083743 interacted with and regulated miR-103-3p, thereby promoting BDNF expression and SC proliferation. BC083743 overexpression also promoted axon regeneration through miR-103-3p. In vivo experiments also indicated that BC083743 overexpression promoted the repair of SNC. In conclusion, LncRNA BC083743 promotes SC proliferation and the axon regeneration through miR-103-3p/BDNF after SNC.