Single Rabbit Stomach Smooth Muscle Cell Myosin Heavy Chain SMB Expression and Shortening Velocity

Document Type

Article

Language

eng

Format of Original

8 p.

Publication Date

2-2001

Publisher

American Physiological Society

Source Publication

American Journal of Physiology - Cell Physiology

Source ISSN

0002-9513

Original Item ID

DOI: 10.1152/ajpcell.2001.280.2.C309

Abstract

Isolated single smooth muscle cells (SMCs) from different regions of the rabbit stomach were used to determine a possible correlation between unloaded shortening velocity and smooth muscle (SM) myosin heavy chain (MHC) S1 head isoform composition (SMA, no head insert; SMB, with head insert). α-Toxin-permeabilized isolated single cells were maximally activated to measure unloaded shortening velocity and subsequently used in an RT-PCR reaction to determine the SMA/SMB content of the same cell. SM MHC SMA and SMB isoforms are uniquely distributed in the stomach with cells from the fundic region expressing little SMB (38.1 ± 7.3% SMB; n = 16); cells from the antrum express primarily SMB (94.9 ± 1.0% SMB; n = 16). Mean fundic cell unloaded shortening velocity was 0.014 ± 0.002 cell lengths/s compared with 0.036 ± 0.002 for the antrum cells. Unloaded shortening velocity in these cells was significantly correlated with their percent SMB expression (r2 = 0.58). Resting cell length does not correlate with the percent SMB expression (n = 32 cells). Previously published assays of purified or expressed SMA and SMB heavy meromyosin show a twofold difference in actin filament sliding speed in in vitro motility assays. Extrapolation of our data to 0-100% SMB would give a 10-fold range of shortening velocity, which is closer to the ~20-fold range reported from various SM tissues. This suggests that mechanisms in addition to the MHC S1 head isoforms regulate shortening velocity.

Comments

American Journal of Physiology - Cell Physiology, Volume 280 (February 2001): C309-C316. DOI.

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