MiR-138-5p targets RUNX2 to inhibit osteogenic differentiation of aortic valve interstitial cells via Wnt/β-catenin signaling pathway

التفاصيل البيبلوغرافية
العنوان: MiR-138-5p targets RUNX2 to inhibit osteogenic differentiation of aortic valve interstitial cells via Wnt/β-catenin signaling pathway
المؤلفون: Fei Yan, Qiang Huo, Weimin Zhang, Tingting Wu, Daniyaer Dilimulati, Lin Shi
المصدر: BMC Cardiovascular Disorders, Vol 22, Iss 1, Pp 1-8 (2022)
BMC Cardiovascular Disorders
بيانات النشر: BMC, 2022.
سنة النشر: 2022
مصطلحات موضوعية: Adult, Male, Wnt/β-catenin, miR-138-5p, Research, RUNX2, Calcinosis, Cell Differentiation, Core Binding Factor Alpha 1 Subunit, Aortic Valve Stenosis, MicroRNAs, Gene Expression Regulation, Calcific aortic valve disease (CAVD), Osteogenesis, Aortic Valve, Osteogenic differentiation, RC666-701, Humans, Diseases of the circulatory (Cardiovascular) system, Female, Aortic valve interstitial cells (AVICs), Cardiology and Cardiovascular Medicine, Wnt Signaling Pathway, Cells, Cultured, beta Catenin
الوصف: Background Human aortic valve interstitial cells (hAVICs) are a key factor in the pathogenesis of calcific aortic valve disease (CAVD). This research examines the role and mechanism of microRNA miR-138-5p in osteogenic differentiation of hAVICs. Methods RT-qPCR analysis was applied for detecting miR-138-5p and RUNX2 expression in valve tissues of CAVD patients and controls. On completion of induction of osteogenic differentiation of hAVICs, and after overexpression or interference of miR-138-5p expression, the condition of osteogenic differentiation and calcification of hAVICs was confirmed using alkaline phosphatase staining and alizarin red staining. Subsequently, western blot was utilized to detect the expression of osteogenesis-related proteins OPN and ALP, and Wnt/β-catenin signaling pathway-related proteins. Finally, the relationship between miR-138-5p and RUNX2 was validated by dual-luciferase reporter assay and Pearson’s correlation test. Results Down-regulation of miR-138-5p was found in CAVD patients and during osteogenic differentiation of hAVICs. Overexpression of miR-138-5p contribute to the inhibition of osteoblast differentiation and calcium deposition in hAVICs, and of ALP and OPN protein expression. RUNX2 was a target gene of miR-138-5p, and it was negatively correlated with miR-138-5p in CAVD. Additionally, overexpression of RUNX2 could reverse the inhibitory effect of miR-138-5p on osteogenic differentiation of hAVICs. Conclusion miR-138-5p can act as a positive regulator of osteogenic differentiation in CAVD patients to involve in inhibiting valve calcification, which is achieved through RUNX2 and Wnt/β-catenin signaling pathway.
اللغة: English
تدمد: 1471-2261
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33bd5933c6f99a56b73ca18104f8455aTest
https://doaj.org/article/f0866dfb20a540fcaad44cebd50df8f1Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....33bd5933c6f99a56b73ca18104f8455a
قاعدة البيانات: OpenAIRE