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Stimulation of vascular smooth muscle cell proliferation by stiff matrix via the IK Ca channel‐dependent Ca 2+ signaling
Author(s) -
Jia Xiaoling,
Yang Qingmao,
Gao Chao,
Chen Xinlan,
Li Yanan,
Su Hao,
Zheng Yufan,
Zhang Shuwen,
Wang Ziyu,
Wang Haikun,
Jiang LinHua,
Sun Yan,
Fan Yubo
Publication year - 2021
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.30349
Subject(s) - vascular smooth muscle , microbiology and biotechnology , cell growth , extracellular , extracellular matrix , intracellular , bapta , mapk/erk pathway , signal transduction , downregulation and upregulation , stimulation , chemistry , ionomycin , biophysics , biology , endocrinology , biochemistry , smooth muscle , gene
Vascular stiffening, an early and common characteristic of cardiovascular diseases (CVDs), stimulates vascular smooth muscle cell (VSMC) proliferation which reciprocally accelerates the progression of CVDs. However, the mechanisms by which extracellular matrix stiffness accompanying vascular stiffening regulates VSMC proliferation remain largely unknown. In the present study, we examined the role of the intermediate‐conductance Ca 2+ ‐activated K + (IK Ca ) channel in the matrix stiffness regulation of VSMC proliferation by growing A7r5 cells on soft and stiff polydimethylsiloxane substrates with stiffness close to these of arteries under physiological and pathological conditions, respectively. Stiff substrates stimulated cell proliferation and upregulated the expression of the IK Ca channel. Stiff substrate‐induced cell proliferation was suppressed by pharmacological inhibition using TRAM34, an IK Ca channel blocker, or genetic depletion of the IK Ca channel. In addition, stiff substrate‐induced cell proliferation was also suppressed by reducing extracellular Ca 2+ concentration using EGTA or intracellular Ca 2+ concentration using BAPTA‐AM. Moreover, stiff substrate induced activation of extracellular signal‐regulated kinases (ERKs), which was inhibited by treatment with TRAM34 or BAPTA‐AM. Stiff substrate‐induced cell proliferation was suppressed by treatment with PD98059, an ERK inhibitor. Taken together, these results show that substrates with pathologically relevant stiffness upregulate the IK Ca channel expression to enhance intracellular Ca 2+ signaling and subsequent activation of the ERK signal pathway to drive cell proliferation. These findings provide a novel mechanism by which vascular stiffening regulates VSMC function.