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C Franzini-Armstrong

Publications and source records attributed to C Franzini-Armstrong.

At least 91 records · Page 5Linked to original sources

Structure of membranes in crayfish muscle: comparison of phasic and tonic fibres.

Membranes of two crayfish muscles with different contraction speeds were studied with freeze-fracture replicas and thin sections. A fast-contracting, short sarcomere phasic muscle, the tail flexor, and a slowly contracting long sarcomere tonic muscle, the carpopodite flexor, were chosen for this study. Membranes examined included the plasmalemma, clefts, T-system, Z-tubules and sarcoplasmic reticulum (SR). We found distinct differences in the distribution of these membranes: T-system and clefts are more elaborate in the tail flexor, while SR is more extensive in the leg flexor. The tail flexor apparently lacks Z-tubules. These differences were more obvious in freeze-fracture replicas than in thin sections. In freeze-fracture replicas, both junctional and non-junctional T-tubule membranes can be distinguished from Z-tubules by content of intramembranous particles. The junctional regions of T-system and surface membranes contain large (10-11 nm) intramembranous particles that are absent from non-junctional parts of these membranes. There is also a class of particles on the junctional SR fracture faces that differs from intramembranous particles on non-junctional SR. These junctional specialization are similar in long and short sarcomere fibres.

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Structure of sarcoplasmic reticulum.

A classification of the sarcoplasmic reticulum (SR) membrane into areas devoted to different functions is described. The junctional (j) SR is covered by feet, it faces towards the transverse tubules, and it is probably devoted to receiving a signal from them. The free (f) SR contains the calcium pump. Isolated SR forms two fractions: light and heavy SR. The heavy fraction is composed of the lateral sacs of the triad, containing calsequestrin, and its membrane comprises both f and j SR. The light fraction is entirely composed of fSR membrane. It is proposed that the feet join jSR membrane to particles contained within the transverse tubules and that they play a direct role in excitation-contraction coupling.

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Aggregates of particles on the plasmalemma of striated muscle from a spider.

Aggregates of large intramembranous particles are described in the surface membrane of muscle fibers of a spider. The particles are continuous with extensions into the extracellular space, forming large complexes. No intramembranous particles are visible at sites of Z line attachment to the plasma membrane.

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Satellite and invasive cells in frog sartorius muscle.

The occurrence and distribution of two cell types associated with normal and denervated frog skeletal muscle fibers are described. The first is the satellite cell. The general appearance and the number of satellite cells are not affected by long-term denervation. The second type of cell is the invasive cell. Invasive cells penetrate across the basal lamina and up to the core of the muscle fiber, without fusing with it. It is suggested that the origin of invasive cells is extramuscular, probably circulatory. Although invasive cells are more numerous in some denervated muscle, it is established that this is not a direct effect of denervation.

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T-tubule swelling in hypertonic solutions: a freeze substitution study.

Striated muscles from Rana pipiens have been exposed for variable periods of time to Ringer solutions made hypertonic by addition of either sucrose or sodium chloride. The muscles have been rapid-frozen and then prepared for electron microscopy by either freeze-substitution, freeze-fracture or cryoultramicrotomy. The only compartment greatly affected by hypertonicity is the transverse tubular system, which is visibly swollen. None of the elements of the sarcoplasmic reticulum increase in size.

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The passive electrical properties of frog skeletal muscle fibres at different sarcomere lengths.

1. The passive electrical properties of frog skeletal muscle fibres have been measured at a number of different sarcomere lengths (from 2-1 to 4-0 micron). The geometrical outline of each fibre was determined from optical cross-sections and sarcomere length was measured by laser beam diffraction. 2. When fibres were stretched to long sarcomere lengths the membrane capacity, Cm, of both normal and detubulated (glycerol-treated) fibres was significantly less than the Cm of fibres at rest length. A significant reduction in membrane conductance of fibres held at long sarcomere lengths was only seen with detubulated fibres. 3. Membrane capacity and membrane conductance have a significant dependence on the cross-sectional area of normal fibres but are independent of cross-sectional area after detubulation. 4. It has been shown that membrane geometry depends on the sarcomere length of the fibre and it is suggested that the passive membrane properties are related to sarcomere length because they depend on membrane geometry. 5. The specific membrane capacity, calculated from the data from detubulated fibres, is 0-8 micronF/cm2. 6. The internal resistivity, Ri, of normal fibres, also depends on sarcomere length between 2-1 and 3-0 micron. At a sarcomere length of 2-1 micron the average Ri is 122 +/- 3 omega. cm (mean +/- S.E. of mean) and at a sarcomere length of 3-0 micron the average Ri is 210 +/- 17 omega. cm (mean +/- S.E. of mean). No further increase in Ri was observed with further increases in sarcomere length.

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Size and shape of transverse tubule openings in frog twitch muscle fibers.

The openings of transverse tubules in frog twitch fibers are described. The tubules open to the extracellular space by a narrow neck, with an inner diameter of 20 nm. The most peripheral portion of the tubules is tortuous and has a variable diameter. The similarity in size of the openings of T tubules and caveolae and the meandering path of the tubules are sufficient to account for the paucity of observed openings.

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

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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Membrane particles and transmission at the triad.

The structure of the membranes limiting the sarcoplasmic reticulum (SR) and transverse (T) tubules in frog and fish muscle fibers has been studied by freeze fracture. Emphasis is placed on the structure of the membranes at the triad, where thin sections have previously shown that rows of regularly disposed "feet" join SR and T exposed fracture faces allows the following conclusions. 1) The SR membrane is continuous and identical in appearance along the whole sarcomere. Thus the SR is a single uninterrupted compartment and it is likely that the major function of the reticulum, calcium accumulation is performed by the membrane limiting the lateral sacs of the triad, as well as the longitudinal tubules. 2) At the level of the junction with the T tublue, the SR presents a strikingly different number, size and arrangement of particles and pits. This distinct portion of the SR membrane extends father than the area covered by the junctional "feet" and no correlation can be found between the disposition of particles within the membrane and that of the feet on the membrane surface. 3) The T system membrane presents few prominent particles on its junctional face, but these are far less numerous than the feet. 4) Thus, no visible preformed channels exist between SR and T system lumina and it is suggested that direct electrical coupling between the two membranes during excitation is unlikely.

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Studies of the triad. IV. Structure of the junction in frog slow fibers.

The structure of the triadic junction in frog slow fibers has been studied and compared with that of twitch fibers. The junctional gap is wider (by approximately 13%) in slow fibers. The junctional feet have the same size and disposition as in twitch fibers, although the size and shape of the junctional areas are different. It is concluded that the role of triads in slow fibers is the same as in twitch fibers

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The structure of a simple Z line.

The structural simplicity of the Z line in fish muscle fibers allows direct visualization of its basic geometry. Models which postulate termination of the I filaments at the edges of the Z line and the direct linkage of I filaments belonging to the two adjacent sarcomeres by Z filaments crossing the whole width of the Z line give the best fit to the electron micrographs. The structure of fish Z lines is not significantly altered by the use of different fixation procedures and by changes in sarcomere length.

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