The tubular vacuolation process in amphibian skeletal muscle

作者: James A Fraser , Jeremy N Skepper , Austin R Hockaday , Christopher L-H Huang1 , None

DOI: 10.1023/A:1005325013355

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摘要: The exposure of amphibian muscle to osmotic shock through the introduction and subsequent withdrawal extracellular glycerol causes ‘vacuolation’ in transverse tubules. Such manoeuvres can also electrically isolate tubules from surface (‘detubulation’), particularly if followed by exposures high [Ca2+] and/or gradual cooling. This study explored factors influencing vacuolation Rana temporaria sartorius muscle. Vacuole formation was detected using phase contrast microscopy trapping or otherwise lissamine rhodamine dye fluorescence within such vacuoles. preparations were examined electron microscopy, for penetration into tubular vacuoles horseradish peroxidase introduced following procedures. These comparisons distinguished first time two types vacuole, ‘open’ ‘closed’, whose lumina respectively continuous with detached remaining space. formed close between Z-lines, but subsequently elongated along longitudinal axis fibres. suggested an involvement membrane material; latter appeared concentrated around Z-lines electron-micrograph stereopairs thick sections. ‘Open’ produced a glycerol-loaded fibre at stage when one would expect net water entry intracellular suggests that vacuole requires active fluid transport response swelling. ‘Closed’ only exposed cooling initial shock. Their densities similar those shown not so treated, suggesting both resulted single process initiated withdrawal. However, ‘closure’ took place well after vacuoles, over 25 min Its course closely paralleled development detubulation reported recently. It irreversible, reversibility formation. findings identify electrophysiological ‘detubulation’ striated initially reversible open is compatible some normal responses physiological stresses as fatigue, whereas irreversible closed might be expected pathological situations dystrophic

参考文章(38)
Navaratnam, Ayettey As, The T-tubule system in the specialized and general myocardium of the rat. Journal of Anatomy. ,vol. 127, pp. 125- 140 ,(1978)
FERDIA A. GALLAGHER, CHRISTOPHER L.-H. HUANG, Osmotic 'detubulation' in frog muscle arises from a reversible vacuolation process. Journal of Muscle Research and Cell Motility. ,vol. 18, pp. 305- 321 ,(1997) , 10.1023/A:1018670025321
A Franco-Obregón, J B Lansman, Mechanosensitive ion channels in skeletal muscle from normal and dystrophic mice. The Journal of Physiology. ,vol. 481, pp. 299- 309 ,(1994) , 10.1113/JPHYSIOL.1994.SP020440
H. Gonzalez-Serratos, A. V. Somlyo, G. McClellan, H. Shuman, L. M. Borrero, A. P. Somlyo, Composition of vacuoles and sarcoplasmic reticulum in fatigued muscle: electron probe analysis. Proceedings of the National Academy of Sciences of the United States of America. ,vol. 75, pp. 1329- 1333 ,(1978) , 10.1073/PNAS.75.3.1329
P R Turner, P Y Fong, W F Denetclaw, R A Steinhardt, Increased calcium influx in dystrophic muscle. Journal of Cell Biology. ,vol. 115, pp. 1701- 1712 ,(1991) , 10.1083/JCB.115.6.1701
R. H. Adrian, L. D. Peachey, Reconstruction of the action potential of frog sartorius muscle The Journal of Physiology. ,vol. 235, pp. 103- 131 ,(1973) , 10.1113/JPHYSIOL.1973.SP010380
P. Fong, P. Turner, W. Denetclaw, R. Steinhardt, Increased activity of calcium leak channels in myotubes of Duchenne human and mdx mouse origin Science. ,vol. 250, pp. 673- 676 ,(1990) , 10.1126/SCIENCE.2173137
M. Endo, Entry of fluorescent dyes into the sarcotubular system of the frog muscle The Journal of Physiology. ,vol. 185, pp. 224- 238 ,(1966) , 10.1113/JPHYSIOL.1966.SP007983