Involvement of BK channel in differentiation of vascular smooth muscle cells induced by mechanical stretch. (February 2015)

• Record Type: Journal Article
• Authors: Wan, Xue-Jiao; Zhao, Hu-Cheng; Zhang, Ping; Huo, Bo; Shen, Bao-Rong; Yan, Zhi-Qiang; Qi, Ying-Xin; Jiang, Zong-Lai
• Is Part Of: International journal of biochemistry & cell biology. Volume 59(2015:Feb.)
• Page Start: 21
• Page End: 29
• Publication Date: 2015-02
• Subjects: Vascular smooth muscle cells -- Differentiation -- Mechanical stretch -- BK channel -- Endoplasmic reticulum stress; Biochemistry -- Periodicals; Cytology -- Periodicals; Biochemistry -- Periodicals; Cell Biology -- Periodicals; Biochimie -- Périodiques; Cytologie -- Périodiques; Biochimie; Cytologie; Biochemistry; Cytology; Ressource Internet (Descripteur de forme); Périodique électronique (Descripteur de forme); Periodicals; 572.05
• DOI: 10.1016/j.biocel.2014.11.011
• Languages: English
• ISSNs: 1357-2725

Abstract

Abstract: The differentiation of vascular smooth muscle cells (VSMCs), which are exposed to mechanical stretch in vivo, plays an important role in vascular remodeling during hypertension. Here, we demonstrated the mechanobiological roles of large conductance calcium and voltage-activated potassium (BK) channels in this process. In comparison with 5% stretch (physiological), 15% stretch (pathological) induced the de-differentiation of VSMCs, resulting in significantly decreased expressions of VSMC markers, i.e., α-actin, calponin and SM22. The activity of BK channels, assessed by patch clamp recording, was significantly increased by 15% stretch and was accompanied by an increased alternative splicing of BK channel α-subunit at the stress axis-regulated exons (STREX). Furthermore, transfection of whole BK or STREX-deleted BK plasmids revealed that STREX was important for BK channels to sense mechanical stretch. Using thapsigargin (TG) which induces endoplasmic reticulum (ER) stress, and xbp1-targeted siRNA transfection which blocks ER stress, the results revealed that ER stress was contribute to stretch-induced alternative splicing of STREX. Our results suggested that during hypertension, pathological stretch may induce the ER stress in VSMCs, which affects the alternative splicing and activity of BK channels, and subsequently modulates VSMC differentiation.