Literature DB >> 1080806

The relative contributions of the folds and caveolae to the surface membrane of frog skeletal muscle fibres at different sarcomere lengths.

A F Dulhunty, C Franzini-Armstrong.   

Abstract

The plasmalemmal area of striated muscle fibres is greater than the apparent surface area (A = circumference x length) because of variable folds and the invaginations of the caveolae and T-tubules. Freeze-fracture replicas of the surface membrane of sartorius and semitendinosus muscles from Rana pipiens have been used to determine the numbers and distribution of folds and caveolae at different sarcomere lengths. (1) The plasmalemma folds are variable in size and shape, but are always oriented perpendicular to the long axis of the fibre. The folds vary with stretch, being more prominent at short sarcomere lengths. The caveolae are elliptical invaginations of the plasmalemma which open to the outside by a narrow "neck" of approximately 20 nm. The caveolar lumen has an average long dimension of 81.6 +/- 11.7 nm and an average short dimension of 66.9 +/- 7.9 nm. The caveolar "necks" only can be seen in freeze-fracture replicas and these are distributed in two circumferential bands on either side of the Z-line, and in longitudinal bands separated by distances of 1-5 mum. In the sartorius muscle, at a sarcomere length of 2.8 mum, there is an average number of thirty-seven caveolae per square micrometer of fibre surface. (2) During passive stretch the opening of folds provides membrane for the necessary increase in surface area up to a sarcomere length of about 3.0 mum. This length is defined as the critical sarcomere length (Sc). The number of caveolae remains constant at all sarcomere lengths less than Sc and thus their "necks" have been used as membrane markers to determine the amount of folding at different sarcomere lengths. The membrane area contained in folds and caveolae is expressed as a fraction of the apparent surface area (A). For example, in the sartorius muscle, at a sarcomere length of 2.4 mum, the membrane area, excluding the T-tubules, is: A + 0.1A (folding) + 0.7A (caveolae) = 1.8A. (3) For stretch beyond Sc membrane is provided by the opening of caveolae. At a sarcomere length of about 8 mum all the caveolae are open and the fibres rupture with further stretch. (4) The relative contributions of folds and caveolae vary with sarcomere length in a way that is consistent with assumptions of constant volume and plasmalemma area. The maintenance of constant plasmalemma area, even after excessive stretch, suggests that the plasmalemma is relatively inelastic in this situation.

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Mesh:

Year:  1975        PMID: 1080806      PMCID: PMC1348391          DOI: 10.1113/jphysiol.1975.sp011068

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  23 in total

1.  Tensile force in total striated muscle, isolated fibre and sarcolemma.

Authors:  C CASELLA
Journal:  Acta Physiol Scand       Date:  1950-12

2.  The sarcolemma of skeletal muscle fibres as demonstrated by a replica technique.

Authors:  H Schmalbruch
Journal:  Cell Tissue Res       Date:  1974       Impact factor: 5.249

3.  Impedance of frog skeletal muscle fibers in various solutions.

Authors:  R Valdiosera; C Clausen; R S Eisenberg
Journal:  J Gen Physiol       Date:  1974-04       Impact factor: 4.086

4.  Electrical properties of toad sartorius muscle fibres in summer and winter.

Authors:  A F Dulhunty; P W Gage
Journal:  J Physiol       Date:  1973-05       Impact factor: 5.182

5.  The distribution of the T-system along the sarcomeres of frog and toad sartorius muscles.

Authors:  L D Peachey; R F Schild
Journal:  J Physiol       Date:  1968-01       Impact factor: 5.182

6.  Surface features of striated muscle. II. Guinea-pig skeletal muscle.

Authors:  D G Rayns; F O Simpson; W S Bertaud
Journal:  J Cell Sci       Date:  1968-12       Impact factor: 5.285

7.  Membrane splitting in freeze-ethching. Covalently bound ferritin as a membrane marker.

Authors:  P Pinto da Silva; D Branton
Journal:  J Cell Biol       Date:  1970-06       Impact factor: 10.539

8.  Demonstration of the outer surface of freeze-etched red blood cell membranes.

Authors:  T W Tillack; V T Marchesi
Journal:  J Cell Biol       Date:  1970-06       Impact factor: 10.539

9.  Double sucrose-gap method applied to single muscle fiber of Xenopus laevis.

Authors:  S Nakajima; J Bastian
Journal:  J Gen Physiol       Date:  1974-02       Impact factor: 4.086

10.  Differentiation of the sarcoplasmic reticulum and T system in developing chick skeletal muscle in vitro.

Authors:  E B Ezerman; H Ishikawa
Journal:  J Cell Biol       Date:  1967-11-01       Impact factor: 10.539

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  77 in total

1.  Vacuole formation in fatigued single muscle fibres from frog and mouse.

Authors:  J Lännergren; J D Bruton; H Westerblad
Journal:  J Muscle Res Cell Motil       Date:  1999-01       Impact factor: 2.698

2.  Mechanosensitivity of N-type calcium channel currents.

Authors:  Barbara Calabrese; Iustin V Tabarean; Peter Juranka; Catherine E Morris
Journal:  Biophys J       Date:  2002-11       Impact factor: 4.033

Review 3.  Mechanotransduction in skeletal muscle.

Authors:  Thomas J Burkholder
Journal:  Front Biosci       Date:  2007-01-01

4.  Mechanosensitive channel properties and membrane mechanics in mouse dystrophic myotubes.

Authors:  Thomas M Suchyna; Frederick Sachs
Journal:  J Physiol       Date:  2007-01-25       Impact factor: 5.182

5.  Significant roles of microtubules in mature striated muscle deduced from the correlation between tubulin and its molecular chaperone alphaB-crystallin in rat muscles.

Authors:  Hyunseok Jee; Takashi Sakurai; Shigeo Kawada; Naokata Ishii; Yoriko Atomi
Journal:  J Physiol Sci       Date:  2009-03-24       Impact factor: 2.781

6.  Tensile strength and dilatational elasticity of giant sarcolemmal vesicles shed from rabbit muscle.

Authors:  J A Nichol; O F Hutter
Journal:  J Physiol       Date:  1996-05-15       Impact factor: 5.182

7.  Biomechanics of the sarcolemma and costameres in single skeletal muscle fibers from normal and dystrophin-null mice.

Authors:  K P García-Pelagio; R J Bloch; A Ortega; H González-Serratos
Journal:  J Muscle Res Cell Motil       Date:  2011-02-11       Impact factor: 2.698

8.  Freeze-fracture studies of muscle caveolae in human muscular dystrophy.

Authors:  E Bonilla; K Fischbeck; D L Schotland
Journal:  Am J Pathol       Date:  1981-08       Impact factor: 4.307

Review 9.  The membrane hypothesis of Duchenne muscular dystrophy: quest for functional evidence.

Authors:  O F Hutter
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

10.  Caveolae act as membrane reserves which limit mechanosensitive I(Cl,swell) channel activation during swelling in the rat ventricular myocyte.

Authors:  Lukasz Kozera; Ed White; Sarah Calaghan
Journal:  PLoS One       Date:  2009-12-14       Impact factor: 3.240

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