Literature DB >> 9234963

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

C Franzini-Armstrong1, F Protasi.   

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.

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Year:  1997        PMID: 9234963     DOI: 10.1152/physrev.1997.77.3.699

Source DB:  PubMed          Journal:  Physiol Rev        ISSN: 0031-9333            Impact factor:   37.312


  222 in total

1.  Differential response of the membrane systems involved in excitation-contraction coupling to early and later postnatal denervation in rat skeletal muscle.

Authors:  H Takekura; N Kasuga
Journal:  J Muscle Res Cell Motil       Date:  1999-04       Impact factor: 2.698

2.  The role of luminal Ca2+ in the generation of Ca2+ waves in rat ventricular myocytes.

Authors:  V Lukyanenko; S Subramanian; I Gyorke; T F Wiesner; S Gyorke
Journal:  J Physiol       Date:  1999-07-01       Impact factor: 5.182

3.  Ca2+ sparks and Ca2+ waves in saponin-permeabilized rat ventricular myocytes.

Authors:  V Lukyanenko; S Gyorke
Journal:  J Physiol       Date:  1999-12-15       Impact factor: 5.182

Review 4.  Luminal loop of the ryanodine receptor: a pore-forming segment?

Authors:  D Balshaw; L Gao; G Meissner
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-30       Impact factor: 11.205

5.  Inhibition of mouse neuromuscular transmission and contractile function by okadaic acid and cantharidin.

Authors:  S J Hong
Journal:  Br J Pharmacol       Date:  2000-07       Impact factor: 8.739

Review 6.  Electrophysiological modeling of cardiac ventricular function: from cell to organ.

Authors:  R L Winslow; D F Scollan; A Holmes; C K Yung; J Zhang; M S Jafri
Journal:  Annu Rev Biomed Eng       Date:  2000       Impact factor: 9.590

7.  Two domains in dihydropyridine receptor activate the skeletal muscle Ca(2+) release channel.

Authors:  M Stange; A Tripathy; G Meissner
Journal:  Biophys J       Date:  2001-09       Impact factor: 4.033

8.  Spark- and ember-like elementary Ca2+ release events in skinned fibres of adult mammalian skeletal muscle.

Authors:  W G Kirsch; D Uttenweiler; R H Fink
Journal:  J Physiol       Date:  2001-12-01       Impact factor: 5.182

9.  Sustained release of calcium elicited by membrane depolarization in ryanodine-injected mouse skeletal muscle fibers.

Authors:  Claude Collet; Vincent Jacquemond
Journal:  Biophys J       Date:  2002-03       Impact factor: 4.033

10.  Mutations to Gly2370, Gly2373 or Gly2375 in malignant hyperthermia domain 2 decrease caffeine and cresol sensitivity of the rabbit skeletal-muscle Ca2+-release channel (ryanodine receptor isoform 1).

Authors:  G G Du; H Oyamada; V K Khanna; D H MacLennan
Journal:  Biochem J       Date:  2001-11-15       Impact factor: 3.857

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