4.7 Review

Functional regulation of large conductance Ca2+-activated K+ channels in vascular diseases

Journal

METABOLISM-CLINICAL AND EXPERIMENTAL
Volume 83, Issue -, Pages 75-80

Publisher

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.metabol.2018.01.008

Keywords

BK channels; Smooth muscle cells; Diabetes mellitus; beta-Subunit

Funding

  1. National Natural Science Foundation of China [81370304, 81770441, 91639303]
  2. Natural Science Foundation of Jiangsu Province [BK20151085]
  3. 10th Summit of Six Top Talents of Jiangsu Province [2016-WSN-185]
  4. Medical Science and Technology Development Foundation of Nanjing Department of Health [YKK15102, ZKX16048]
  5. Jiangsu Province High Level Innovation and Entrepreneurship Talent Introduction Plan [2015-395]

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The large conductance Ca2+-activated potassium channels, the BK channels, is widely expressed in various tissues and activated in a Ca2+- and voltage-dependent manner. The activation of BK channels hyperpolarizes vascular smooth muscle cell membrane potential, resulting in vasodilation. Under pathophysiological conditions, such as diabetes mellitus and hypertension, impaired BK channel function exacerbates vascular vasodilation and leads to organ ischemia. The vascular BK channel is composed of 4 pore-forming subunits, BK-alpha together with 4 auxiliary subunits: beta(1) subunits (BK-beta(1)) or gamma(1) subunits (BK-gamma(1)). Recent studies have shown that down-regulation of the BK beta(1) subunit in diabetes mellitus induced vascular dysfunction; however, the molecular mechanism of these vascular diseases is not well understood. In this review, we summarize the potential mechanisms regarding BK channelopathy and the potential therapeutic targets of BK channels for vascular diseases. (C) 2018 Elsevier Inc. All rights reserved.

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