Home LiteratureArticle Details
PMID: 11827959 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Capacitative calcium entry contributes to nuclear factor of activated T-cells nuclear translocation and hypertrophy in cardiomyocytes.

The Journal of biological chemistry ·Vol. 277 ·No. 16 ·2002-04-19 ·Pages 14266-73

Hunton DL, Lucchesi PA, Pang Y, Cheng X, Dell'Italia LJ, Marchase RB

Abstract

In nonexcitable cells, depletion of endoplasmic reticulum Ca(2+) stores leads to activation of plasma membrane Ca(2+) channels, a process termed capacitative Ca(2+) entry. Here, we demonstrate that this pathway functions in cells that also contain voltage-gated Ca(2+) channels, neonatal rat ventricular myocytes. The depletion of sarcoplasmic reticulum Ca(2+) stores elicited a prolonged increase in cytoplasmic Ca(2+) dependent on extracellular Ca(2+). Inhibitors of store-operated channels but not L-type channels diminished this response. The importance of this pathway to cardiac hypertrophy, which often is dependent on Ca(2+)/calmodulin-dependent transcription factors, was also assessed in this model. Hypertrophy and atrial natriuretic factor expression induced by angiotensin II or phenylephrine was more effectively attenuated by inhibitors of capacitative entry than of L-type channels. Additionally, cardiomyocytes were transfected with a construct encoding a fluorescent nuclear factor of activated T-cells chimeric protein to follow nuclear localization in response to thapsigargin, angiotensin II, and phenylephrine. This translocation was completely prevented by inhibitors of capacitative Ca(2+) entry and only partially abrogated by inhibitors of L-type channels. In contrast, a hypertrophic response induced by overexpression of the transcription factor MEK1 was unaffected by inhibitors of capacitative entry. Together, these data suggest a role for CCE in cardiomyocyte physiology and, in particular, in Ca(2+)-mediated cardiac hypertrophy.

MeSH Terms
Active Transport, Cell Nucleus Adenoviridae/metabolism Angiotensin II/pharmacology Animals Calcium/metabolism Calcium Channels/metabolism Cells, Cultured Cytoplasm/metabolism DNA-Binding Proteins/metabolism Green Fluorescent Proteins Immunohistochemistry Luminescent Proteins/metabolism MAP Kinase Kinase 1 Microscopy, Confocal Microscopy, Fluorescence Mitogen-Activated Protein Kinase Kinases/metabolism Myocardium/cytology NFATC Transcription Factors Nuclear Proteins Phenylephrine/pharmacology Protein Serine-Threonine Kinases/metabolism Rats Rats, Sprague-Dawley Recombinant Fusion Proteins/metabolism Time Factors Transcription Factors/metabolism Transfection
Chemicals
Calcium Channels DNA-Binding Proteins Luminescent Proteins NFATC Transcription Factors Nuclear Proteins Recombinant Fusion Proteins Transcription Factors Angiotensin II Green Fluorescent Proteins Phenylephrine Protein Serine-Threonine Kinases MAP Kinase Kinase 1 Mitogen-Activated Protein Kinase Kinases Calcium
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Hunton Dacia L
Department of Cell Biology, University of Alabama, Birmingham 35294-0005, USA.
Lucchesi Pamela A
Pang Yi
Cheng Xiaogang
Dell'Italia Louis J
Marchase Richard B
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2002-04-19
Epub
2002-00-04
Pages
14266-73
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIDDK NIH HHS · DK 55647 · United States
NHLBI NIH HHS · HL 60707 · United States
NHLBI NIH HHS · T32 HL07918 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com