Activation of Ca2+-activated Cl- channel ANO1 by localized Ca2+ signals

被引:53
|
作者
Jin, Xin [1 ]
Shah, Sihab [1 ]
Du, Xiaona [2 ]
Zhang, Hailin [2 ]
Gamper, Nikita [1 ,2 ]
机构
[1] Univ Leeds, Fac Biol Sci, Sch Biomed Sci, Leeds LS2 9JT, W Yorkshire, England
[2] Hebei Med Univ, Dept Pharmacol, Shijiazhuang, Peoples R China
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2016年 / 594卷 / 01期
基金
英国惠康基金; 美国国家科学基金会;
关键词
SMOOTH-MUSCLE-CELLS; TMEM16A CHLORIDE CHANNEL; RAT SENSORY NEURONS; INTERSTITIAL-CELLS; ANOCTAMIN; CAPSAICIN RECEPTOR; CURRENT EXPRESSION; ION-TRANSPORT; NERVE-INJURY; CALCIUM;
D O I
10.1113/jphysiol.2014.275107
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Ca2+-activated chloride channels (CaCCs) regulate numerous physiological processes including epithelial transport, smooth muscle contraction and sensory processing. Anoctamin-1 (ANO1, TMEM16A) is a principal CaCC subunit in many cell types, yet our understanding of the mechanisms of ANO1 activation and regulation are only beginning to emerge. Ca2+ sensitivity of ANO1 is rather low and at negative membrane potentials the channel requires several micromoles of intracellular Ca2+ for activation. However, global Ca2+ levels in cells rarely reach such levels and, therefore, there must be mechanisms that focus intracellular Ca2+ transients towards the ANO1 channels. Recent findings indeed indicate that ANO1 channels often co-localize with sources of intracellular Ca2+ signals. Interestingly, it appears that in many cell types ANO1 is particularly tightly coupled to the Ca2+ release sites of the intracellular Ca2+ stores. Such preferential coupling may represent a general mechanism of ANO1 activation in native tissues.
引用
收藏
页码:19 / 30
页数:12
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