Home LiteratureArticle Details
PMID: 9234963 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

Ryanodine receptors of striated muscles: a complex channel capable of multiple interactions.

Physiological reviews ·Vol. 77 ·No. 3 ·1997-07-00 ·Pages 699-729

Franzini-Armstrong C, Protasi F

Abstract

The ryanodine receptor (RyR) is a high-conductance Ca2+ channel of the sarcoplasmic reticulum in muscle and of the endoplasmic reticulum in other cells. In striated muscle fibers, RyRs are responsible for the rapid release of Ca2+ that activates contraction. Ryanodine receptors are complex molecules, with unusually large cytoplasmic domains containing numerous binding sites for agents that control the state of activity of the channel-forming domain of the molecule. Structural considerations indicate that long-range interactions between cytoplasmic and intramembrane domains control channel function. Ryanodine receptors are located in specialized regions of the SR, where they are structurally and functionally associated with other intrinsic proteins and, indirectly, also with the luminal Ca2(+)-binding protein calsequestrin. Activation of RyRs during the early part of the excitation-contraction coupling cascade is initiated by the activity of surface-membrane Ca2+ channels, the dihydropyridine receptors (DHPRs). Skeletal and cardiac muscles contain different RyR and DHPR isoforms and both contribute to the diversity in cardiac and skeletal excitation-contraction coupling mechanisms. The architecture of the sarcoplasmic reticulum-surface junctions determines the types of RyR-DHPR interactions in the two muscle types.

MeSH Terms
Animals Calcium Channels/analysis,chemistry,physiology Calcium Channels, L-Type Endoplasmic Reticulum/chemistry,physiology,ultrastructure Heart/physiology Humans Isomerism Muscle Proteins/analysis,chemistry,physiology Muscle, Skeletal/chemistry,physiology,ultrastructure Myocardium/chemistry,ultrastructure Ryanodine Receptor Calcium Release Channel Sarcoplasmic Reticulum/chemistry,physiology,ultrastructure
Chemicals
Calcium Channels Calcium Channels, L-Type Muscle Proteins Ryanodine Receptor Calcium Release Channel
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Franzini-Armstrong C
Department of Cell and Developmental Biology, University of Pennsylvania, Philadelphia, USA.
Protasi F
Article Info
Journal
Physiological reviews
Abbr.
Physiol Rev
ISSN
0031-9333
Published
1997-07-00
Pages
699-729
Language
English
Region
United States
NLM ID
0231714
Subset
IM
Grants
NHLBI NIH HHS · HL-15835 · United States
NHLBI NIH HHS · R01-HL-48093 · 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