Literature DB >> 34997455

Circ_0092291 attenuates angiotensin II-induced cell damages in human aortic vascular smooth muscle cells via mediating the miR-626/COL4A1 signal axis.

Ming Ma1, Xiaofei Yang2, Feng Han2, Haidong Wang2.   

Abstract

Abdominal aortic aneurysm (AAA) is a potentially fatal vascular disease, and the dysregulated circular RNAs (circRNAs) play key roles in AAA progression. Circ_0092291 was downregulated in AAA patients, but its function in AAA remains unclear. This research was performed for the functional analysis of circ_0092291 and its mechanism exploration with mircoRNA-626 (miR-626) and collagen type IV alpha1 chain (COL4A1) in AAA. Human aortic vascular smooth muscle cells (T/G HA-VSMC) were treated with angiotensin II (Ang II). Levels of circ_0092291, miR-626, and COL4A1 were determined using reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Inflammatory cytokines were examined by enzyme-linked immunosorbent assay (ELISA). Cell apoptosis was measured using caspase3 activity assay and flow cytometry. Angiopoiesis was assessed via tube formation assay. The protein analysis was conducted by western blot. Dual-luciferase reporter assay, RNA immunoprecipitation (RIP), and RNA pull-down assays were used to validate the molecular binding. Circ_0092291 downregulation was found in AAA samples and Ang II-treated cells. Inflammatory response and cell apoptosis were reduced while angiopoiesis and ECM level were facilitated after overexpression of circ_0092291 in Ang II-treated T/G HA-VSMC cells. MiR-626 was a miRNA target for circ_0092291, and miR-626 inhibition protected T/G HA-VSMC from Ang II-induced cell injury. Moreover, the regulation of circ_0092291 was achieved by serving as a miR-626 sponge in Ang II-treated cells. COL4A1 was affirmed as a target for miR-626 and circ_0092291 resulted in the level change of COL4A1 by sponging miR-626. Additionally, miR-626 downregulation inhibited the cell damages caused by Ang II through increasing the level of COL4A1 and the function of circ_0092291 was attributed to the upregulation of COL4A1. The evidence indicated that circ_0092291 could suppress the Ang II-induced cell dysfunction by targeting the miR-626/COL4A1 signaling axis. Circ_0092291 might improve the diagnosis and treatment of AAA.Key Points.Biological mechanism, Apoptosis, Molecular target.
© 2021. The Author(s) under exclusive licence to University of Navarra.

Entities:  

Keywords:  Abdominal aortic aneurysm; COL4A1; Circ_0092291; miR-626

Mesh:

Substances:

Year:  2022        PMID: 34997455     DOI: 10.1007/s13105-021-00859-0

Source DB:  PubMed          Journal:  J Physiol Biochem        ISSN: 1138-7548            Impact factor:   4.158


  3 in total

1.  MicroRNA-423 enhances the invasiveness of hepatocellular carcinoma via regulation of BRMS1.

Authors:  Xiangjun Sun; Mingchun Wang; Haiyan Liu; Jian Wang
Journal:  Am J Transl Res       Date:  2017-12-15       Impact factor: 4.060

2.  Knockdown of lncRNA PVT1 Inhibits Vascular Smooth Muscle Cell Apoptosis and Extracellular Matrix Disruption in a Murine Abdominal Aortic Aneurysm Model.

Authors:  Zhidong Zhang; Gangqiang Zou; Xiaosan Chen; Wei Lu; Jianyang Liu; Shuiting Zhai; Gang Qiao
Journal:  Mol Cells       Date:  2019-02-01       Impact factor: 5.034

3.  CDR1as/miR-7/CKAP4 axis contributes to the pathogenesis of abdominal aortic aneurysm by regulating the proliferation and apoptosis of primary vascular smooth muscle cells.

Authors:  Feng Zhao; Tongyun Chen; Nan Jiang
Journal:  Exp Ther Med       Date:  2020-03-23       Impact factor: 2.447

  3 in total
  1 in total

1.  Activating transcription factor 4 aggravates angiotensin II-induced cell dysfunction in human vascular aortic smooth muscle cells via transcriptionally activating fibroblast growth factor 21.

Authors:  Ke Tao; Ming Li; Xuefeng Gu; Ming Wang; Tianwei Qian; Lijun Hu; Jiang Li
Journal:  Korean J Physiol Pharmacol       Date:  2022-09-01       Impact factor: 1.718

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.