The Long Noncoding RNA LINC00963 Inhibits Corneal Fibrosis Scar Formation by Targeting miR-143-3p.

Abstract

Corneal fibrosis is a complication of severe corneal injury, one of the major causes of vision loss. The formation of myofibroblasts has emerged as a key stimulative factor of corneal fibrosis. In the current study, we focused on the role of LINC00963 in regulating corneal fibrosis. Transforming growth factor β1 (TGF-β1) was used to induce human corneal stromal cells differentiating into corneal myofibroblasts, and the significant increase of α-smooth muscle actin (α-SMA) was verified by quantitative real-time PCR (qRT-PCR), western blot, and immunofluorescence, respectively. LINC00963 was identified to be one-half decreased compared with nonstimulated human corneal stromal cells, indicating that it might play a role in corneal fibrosis. Interestingly, overexpression of LINC00963 resulted in decreased formation of myofibroblasts indicating that it might exhibit an inhibiting effect. Moreover, bioinformatics tool was applied to predict the downstream target of LINC00963. We investigated that LINC00963 suppressed α-SMA induced by TGF-β1 in corneal fibroblasts, at least in part, by downregulating the expression of miR-143-3p. In addition, either LINC00963 promotion or miR-143-3p inhibition could significantly decrease myofibroblast contractility and collagen I and III secretion, which are the key to contribute to corneal fibrosis. Taken together, our study identified LINC00963 as a promising therapeutic target.

• Authors: Lixia Zhang, Jinning Gao, Anjing Gong, Yanhan Dong, Xiaodan Hao, Xuekang Wang, Jian Zheng, Wenmeng Ma, Yiying Song, Jie Zhang, Wenhua Xu
• Journal: DNA and cell biology (DNA Cell Biol) Vol. 41 Issue 4 Pg. 400-409 (Apr 2022) ISSN: 1557-7430 [Electronic] United States
• PMID: 35262384 (Publication Type: Journal Article)

Chemical References

• Actins
• MIRN143 microRNA, human
• MicroRNAs
• RNA, Long Noncoding
• Transforming Growth Factor beta1
• long non-coding RNA LINC00963, human

Topics

• Actins (genetics, metabolism)
• Cells, Cultured
• Cicatrix (metabolism)
• Corneal Injuries (genetics, metabolism)
• Fibroblasts (metabolism)
• Fibrosis
• Humans
• MicroRNAs (genetics, metabolism)
• RNA, Long Noncoding (genetics, metabolism)
• Transforming Growth Factor beta1 (pharmacology)