» Articles » PMID: 4264604

Ultrastructure of Barnacle Giant Muscle Fibers

Overview
Journal J Cell Biol
Specialty Cell Biology
Date 1973 Jan 1
PMID 4264604
Citations 37
Authors
Affiliations
Soon will be listed here.
Abstract

Increasing use of barnacle giant muscle fibers for physiological research has prompted this investigation of their fine structure. The fibers are invaginated by a multibranched system of clefts connecting to the exterior and filled with material similar to that of the basement material of the sarcolemmal complex. Tubules originate from the surface plasma membrane at irregular sites, and also from the clefts They run transversely, spirally, and longitudinally, making many diadic and some triadic contacts with cisternal sacs of the longitudinal sarcoplasmic reticulum. The contacts are not confined to any particular region of the sarcomere. The tubules are wider and their walls are thicker at points of contact with Z material. Some linking of the Z regions occurs across spaces within the fiber which contain large numbers of glycogen particles. A-band lengths are extremely variable, in the range 2.2 microm-20.3 microm (average 5.2 microm) Individual thick filaments have thin (110 A) hollow regions alternating with thick (340 A) solid ones. Bridges between thick filaments occur at random points and are not concentrated into an M band The thin:thick filament ratio is variable in different parts of a fiber, from 3:1 to 6:1. Z bands are basically perforated, but the number of perforations may increase during contraction.

Citing Articles

Regulation of myocardial contraction as revealed by intracellular Ca measurements using aequorin.

Kurihara S, Fukuda N J Physiol Sci. 2024; 74(1):12.

PMID: 38383293 PMC: 10882819. DOI: 10.1186/s12576-024-00906-7.


Microfluorometric analyses of glycogen in freshly dissected, single skeletal muscle fibres of the cane toad using a mechanically skinned fibre preparation.

Nguyen L, Stephenson D, STEPHENSON G J Muscle Res Cell Motil. 1998; 19(6):631-8.

PMID: 9742447 DOI: 10.1023/a:1005377030193.


Characterization of troponin-C interactions in skinned barnacle muscle: comparison with troponin-C from rabbit striated muscle.

Gordon A, Qian Y, Luo Z, Wang C, Mondares R, Martyn D J Muscle Res Cell Motil. 1998; 18(6):643-53.

PMID: 9429158 DOI: 10.1023/a:1018631806182.


Effect of pentachlorophenol on calcium accumulation in barnacle muscle cells.

Nwoga J, Sniffen J, Pena-Rasgado C, Kimler V J Physiol. 1996; 491 ( Pt 1):13-20.

PMID: 9011605 PMC: 1158755. DOI: 10.1113/jphysiol.1996.sp021192.


Excitation-contraction coupling in crustacea: do studies on these primitive creatures offer insights about EC coupling more generally?.

Palade P, Gyorke S J Muscle Res Cell Motil. 1993; 14(3):283-7.

PMID: 8395541 DOI: 10.1007/BF00123092.


References
1.
Gayton D, HINKE J . The location of chloride in single striated muscle fibers of the giant barnacle. Can J Physiol Pharmacol. 1968; 46(2):213-9. DOI: 10.1139/y68-035. View

2.
Franzini-Armstrong C . Natural variability in the length of thin and thick filaments in single fibres from a crab, Portunus depurator. J Cell Sci. 1970; 6(2):559-92. DOI: 10.1242/jcs.6.2.559. View

3.
Ashley C, Ridgway E . On the relationships between membrane potential, calcium transient and tension in single barnacle muscle fibres. J Physiol. 1970; 209(1):105-30. PMC: 1396043. DOI: 10.1113/jphysiol.1970.sp009158. View

4.
BITTAR E, Chen S, Danielson B, HARTMANN H, Tong E . An investigation of sodium transport in barnacle muscle fibres by means of the microsyringe technique. J Physiol. 1972; 221(2):389-414. PMC: 1331339. DOI: 10.1113/jphysiol.1972.sp009757. View

5.
HUXLEY A . Muscle structure and theories of contraction. Prog Biophys Biophys Chem. 1957; 7:255-318. View