Capturing single L-type Ca2+ channel function with optics

被引:10
作者
Nystoriak, Matthew A. [1 ]
Nieves-Cintron, Madeline [1 ]
Navedo, Manuel F. [1 ]
机构
[1] Univ Calif Davis, Dept Pharmacol, Davis, CA 95616 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2013年 / 1833卷 / 07期
基金
美国国家卫生研究院;
关键词
Calcium sparklet; Coupled gating; TIRE; ARTERIAL SMOOTH-MUSCLE; ACTIVATED T-CELLS; CALCIUM SPARKLETS; ANGIOTENSIN-II; BLOOD-PRESSURE; NUCLEAR FACTOR; CALCINEURIN; CA(V)1.2; PROTEIN; NFAT;
D O I
10.1016/j.bbamcr.2012.10.027
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Advances in imaging technology have allowed optical analysis of Ca2+-permeable ion channel activity. Here, we briefly review novel developments in optical recording of L-type voltage-dependent Ca2+ channel (LTCC) function with high spatial and temporal resolution. Underlying principles supporting the use of total internal reflection fluorescence (TIRE) microscopy for optical measurement of channel activity and new functional characteristics of LTCCs revealed by application of this approach are discussed. Visualization of Ca2+ influx through single LTCCs ("LTCC sparklets") has demonstrated that channel activity is regionally heterogeneous and that clustered channels are capable of operating in a cooperative, or "coupled" manner. In light of these findings, we describe a current molecular model for the local control of LTCC activity and coupled gating in physiological and pathological contexts. This article is part of a Special Issue entitled: 12th European Symposium on Calcium. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:1657 / 1664
页数:8
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