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Article type: Research Article
Authors: Wang, Yishenga; 1 | Pei, Wenb; 1 | Lu, Pinga; *
Affiliations: [a] Department of Cardiology, Shanghai Municipal Hospital of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, China | [b] Department of Cardiology, Jingan Hospital of Traditional Chinese Medicine, Shanghai, China
Correspondence: [*] Corresponding author: Ping Lu, Department of Cardiology, Shanghai Municipal Hospital of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, China. Tel.: +86 021 56639828; E-mail: [email protected].
Note: [1] These authors contributed equally to this work.
Abstract: BACKGROUND:Circular RNA (circRNA) is considered to be an important regulator of human diseases, including atherosclerosis (AS). However, the role of circ_ARHGAP32 in AS formation needs further confirmation. OBJECTIVE:To explore the role of circ_ARHGAP32 in AS formation. METHODS:Oxidized low density lipoprotein (ox-LDL) was used to treat vascular smooth muscle cells (VSMCs) to mimic AS cell models in vitro. The expression of circ_ARHGAP32, microRNA (miR)-665, and fibroblast growth factor 2 (FGF2) was analyzed by quantitative real-time PCR. VSMCs function was measured by EdU assay, cell counting kit 8 assay and transwell assay. Protein expression was determined using western blot analysis. Dual-luciferase reporter assay and RNA pull-down assay were performed to verify RNA interaction. RESULTS:Circ_ARHGAP32 was highly expressed in AS patients and ox-LDL-induced VSMCs. Knockdown of circ_ARHGAP32 repressed ox-LDL-induced proliferation and migration in VSMCs. Circ_ARHGAP32 sponged miR-665 to positively regulate FGF2. MiR-665 inhibitor reversed the regulation of sh-circ_ARHGAP32 on ox-LDL-induced VSMCs proliferation and migration. MiR-665 also had a suppressive effect on the proliferation and migration of ox-LDL-induced VSMCs, and this effect could be reversed by FGF2 overexpression. CONCLUSIONS:Circ_ARHGAP32 might be a potential target for AS treatment, which promoted ox-LDL-induced VSMCs proliferation and migration by regulating miR-665/FGF2 network.
Keywords: Atherosclerosis, circ_ARHGAP32, miR-665, FGF2
DOI: 10.3233/CH-221469
Journal: Clinical Hemorheology and Microcirculation, vol. 82, no. 2, pp. 169-182, 2022
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