Literature DB >> 22975345

Total internal reflection fluorescence imaging of Ca(2+)-induced Ca(2+) release in mouse urinary bladder smooth muscle cells.

Hisao Yamamura1, Yuji Imaizumi.   

Abstract

In smooth muscles (SMs), cytosolic Ca(2+) ([Ca(2+)](cyt)) dynamics during an action potential are triggered by Ca(2+) influx through voltage-dependent Ca(2+) channels (VDCCs) in the plasma membrane. The physiological significance of Ca(2+) amplification by subsequent Ca(2+) release through ryanodine receptors (RyRs) from the sarcoplasmic reticulum (SR) is still a matter of topics in SMs. In the present study, depolarization-evoked local Ca(2+) dynamics in Ca(2+) microdomain were imaged using total internal reflection fluorescence (TIRF) microscopy in mouse urinary bladder SM cells (UBSMCs). Upon depolarization under whole-cell voltage-clamp, the rapid and local elevation of [Ca(2+)](cyt) was followed by larger [Ca(2+)](cyt) increase with propagation occurred in a limited TIRF zone within ~200nm from cell surface. The depolarization-evoked [Ca(2+)](cyt) increase in a TIRF zone was abolished or greatly reduced by the pretreatment with Cd(2+) or ryanodine, respectively. The initial local [Ca(2+)](cyt) increases were mediated by Ca(2+) influx through single or clustered VDCCs as Ca(2+) sparklets, and the following step was elicited by Ca(2+)-induced Ca(2+) release (CICR) through RyR from SR. The depolarization-induced outward currents, mainly due to large-conductance Ca(2+)-activated K(+) channel activation, were also markedly reduced by Cd(2+) and ryanodine. In addition, TIRF analyses showed that the fluorescent signals of individual or clustered VDCC distributed in relatively uniform fashion and that a subset of RyRs in the subplasmalemmal SR also located in TIRF zone. In conclusion, fast TIRF imaging successfully demonstrated two step Ca(2+) events upon depolarization in Ca(2+) microdomain of UBSMCs; the initial Ca(2+) influx as Ca(2+) sparklets through discrete VDCC or their clusters and the following CICR via the activation of loosely coupled RyRs in SR located in the Ca(2+) microdomains.
Copyright © 2012 Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22975345     DOI: 10.1016/j.bbrc.2012.08.145

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  4 in total

1.  Caveolin-1 facilitates the direct coupling between large conductance Ca2+-activated K+ (BKCa) and Cav1.2 Ca2+ channels and their clustering to regulate membrane excitability in vascular myocytes.

Authors:  Yoshiaki Suzuki; Hisao Yamamura; Susumu Ohya; Yuji Imaizumi
Journal:  J Biol Chem       Date:  2013-11-07       Impact factor: 5.157

2.  A junctophilin-caveolin interaction enables efficient coupling between ryanodine receptors and BKCa channels in the Ca2+ microdomain of vascular smooth muscle.

Authors:  Takanori Saeki; Yoshiaki Suzuki; Hisao Yamamura; Hiroshi Takeshima; Yuji Imaizumi
Journal:  J Biol Chem       Date:  2019-07-15       Impact factor: 5.157

3.  L-type Ca2+ channel sparklets revealed by TIRF microscopy in mouse urinary bladder smooth muscle.

Authors:  Peter Sidaway; Noriyoshi Teramoto
Journal:  PLoS One       Date:  2014-04-03       Impact factor: 3.240

4.  Reduced Ca2+ spark activity contributes to detrusor overactivity of rats with partial bladder outlet obstruction.

Authors:  Ji Zheng; Hao Zhou; Mengjun Yang; Siji Song; Qiang Dai; Guangju Ji; Zhansong Zhou
Journal:  Aging (Albany NY)       Date:  2020-02-29       Impact factor: 5.682

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.