Journal article
Imaging microdomain Ca2+ in muscle cells
Circulation research, Vol.94(8), pp.1011-1022
04/30/2004
DOI: 10.1161/01.RES.0000125883.68447.A1
PMID: 15117829
Abstract
Ca2+ ions passing through a single or a cluster of Ca2+-permeable channels create microscopic, short-lived Ca2+ gradients that constitute the building blocks of cellular Ca2+ signaling. Over the last decade, imaging microdomain Ca2+ in muscle cells has unveiled the exquisite spatial and temporal architecture of intracellular Ca2+ dynamics and has reshaped our understanding of Ca2+ signaling mechanisms. Major advances include the visualization of "Ca2+ sparks" as the elementary events of Ca2+ release from the sarcoplasmic reticulum (SR), "Ca2+ sparklets" produced by openings of single Ca2+-permeable channels, miniature Ca2+ transients in single mitochondria ("marks"), and SR luminal Ca2+ depletion transients ("scraps"). As a model system, a cardiac myocyte contains a 3-dimensional grid of 104 spark ignition sites, stochastic activation of which summates into global Ca2+ transients. Tracking intermolecular coupling between single L-type Ca2+ channels and Ca2+ sparks has provided direct evidence validating the local control theory of Ca2+-induced Ca2+ release in the heart. In vascular smooth muscle myocytes, Ca2+ can paradoxically signal both vessel constriction (by global Ca2+ transients) and relaxation (by subsurface Ca2+ sparks). These findings shed new light on the origin of Ca2+ signaling efficiency, specificity, and versatility. In addition, microdomain Ca2+ imaging offers a novel modality that complements electrophysiological approaches in characterizing Ca2+ channels in intact cells.
Details
- Title: Subtitle
- Imaging microdomain Ca2+ in muscle cells
- Creators
- Shi-Qiang Wang - National Institute on AgingChaoliang Wei - Peking UniversityGuiling Zhao - Southern Medical UniversityDidier X P Brochet - National Institutes of HealthJianxin Shen - National Institutes of HealthLong-Sheng Song - National Institutes of HealthWang Wang - National Institutes of HealthDongmei Yang - Peking UniversityHeping Cheng - National Institutes of Health
- Resource Type
- Journal article
- Publication Details
- Circulation research, Vol.94(8), pp.1011-1022
- DOI
- 10.1161/01.RES.0000125883.68447.A1
- PMID
- 15117829
- NLM abbreviation
- Circ Res
- ISSN
- 0009-7330
- eISSN
- 1524-4571
- Language
- English
- Date published
- 04/30/2004
- Academic Unit
- Cardiovascular Medicine; Fraternal Order of Eagles Diabetes Research Center; Biochemistry and Molecular Biology; Internal Medicine
- Record Identifier
- 9984293088102771
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