Modal gating in neuronal and skeletal muscle ryanodine-sensitive Ca2+ release channels

• Published in: The American journal of physiology Vol. 271; no. 1 Pt 1; p. C144
• Main Authors: Armisén, R, Sierralta, J, Vélez, P, Naranjo, D, Suárez-Isla, B A
• Format: Journal Article
• Language: English
• Published: United States 01.07.1996
• Subjects: Animals; Anura; Calcium - pharmacology; Calcium Channels - drug effects; Calcium Channels - metabolism; Chickens; Homeostasis; Ion Channel Gating; Kinetics; Models, Biological; Muscle, Skeletal - metabolism; Neurons - metabolism; Rabbits; Rats; Ryanodine - pharmacology; Time Factors
• ISSN: 0002-9513
• DOI: 10.1152/ajpcell.1996.271.1.C144

The bursting behavior of ryanodine-sensitive single Ca2+ release channels present in chicken cerebellum endoplasmic reticulum (ER), rat hippocampus ER, and frog and rabbit skeletal muscle sarcoplasmic reticulum was established. Unconditional dwell time distributions fitted by the maximum likelihood method reveal at least three open and closed exponential components. Trains of low open probability (P(o)) bursts were interspersed with trains of high P(o) bursts (> or = 0.8) in all the ryanodine receptor isotypes tested. The gating kinetics of the Ca2+ release channels were defined in long recordings by analyzing burst sequences and gamma distributions of average intraburst open (T(o)) and closed times (Tc). The gamma distributions of T(o) had two gamma components, suggesting the existence of two distinct burst types. In contrast, the gamma distributions of Tc had only one component. The correlation between consecutive burst pairs was defined in terms of T(o) and then statistically tested by 2 x 2 matrix contingency analysis. The probability that the ubiquitous sequential burst pattern was generated by random occurrence was < 0.01 (two-tailed Fisher's exact test). Temporal correlations were observed in all ryanodine receptor isotypes under a variety of experimental conditions. These data strongly suggest that single Ca2+ release channels switch slowly between modes of gating. We propose that the effects of agonists of Ca2+ release channels such as Ca2+ itself can be explained as concentration-dependent changes in the availability of each mode.