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Ultrastructural and Physiological Studies on the Longitudinal Body Wall Muscle of Dolabella auricularia: I. Mechanical Response and Ultrastructure

Haruo Sugi and Suechika Suzuki
The Journal of Cell Biology
Vol. 79, No. 2, Part 1 (Nov., 1978), pp. 454-466
Stable URL: http://www.jstor.org/stable/3526776
Page Count: 13
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Ultrastructural and Physiological Studies on the Longitudinal Body Wall Muscle of Dolabella auricularia: I. Mechanical Response and Ultrastructure
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Abstract

The physiological properties of mechanical response and the ultrastructure in the longitudinal body wall muscle (LBWM) of the opisthobranch mollusc Dolabella auricularia were studied to obtain information about excitation-contraction coupling in somatic smooth muscles responsible for smooth and slow body movement of molluscans. The contracture tension produced by 400 mM K was not affected by Mn ions (5-10 mM) and low pH (up to 4.0), but was reduced by procaine (2 mM). The K-contracture tension was not readily eliminated in a Ca-free solution containing ethylene glycol-bis(β-aminoethyl ether)N,N,N′,N′-tetraacetate (EGTA). A large contracture tension was also produced by rapid cooling of the surrounding fluid from 20° to 5°-3°C even when the preparation showed no mechanical response to 400 mM K after prolonged (more than 2 h) soaking in the Ca-free solution. These results indicate that the LBWM fibers contain a large amount of intracellularly stored Ca which can be effectively released by membrane depolarization. The fibers were connected with each other, forming the gap junctions, the desmosomes, and the intermediate junctions. The sarcoplasmic reticulum (SR) consisted of vesicular and tubular elements, and was mostly located near the fiber surface. The plasma membrane showed marked tubular invaginations of 600-800 Å in diameter, with many branches (surface tubules), extending inwards for ∼2 μm. These surface tubules were closely apposed to the SR, and the bridgelike structures analogous to those in the triadic junction of vertebrate skeletal muscle were observed in the space between the surface tubules and the SR. It is suggested that the influence of membrane depolarization is transmitted inwards along the surface tubules to cause the release of Ca from the SR.

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