Form follows function: How muscle shape is regulated by work

Journal of Applied Physiology

Volumn 88, Issue 3, 2000, Pages 1127-1132

  Russell, Brenda ^a,b   Motlagh, Delara ^a   Ashley, William W ^a  

^a UNIVERSITY OF ILLINOIS   (United States)

^b UNIVERSITY OF ILLINOIS AT CHICAGO   (United States)

Author keywords

Assembly; Cardiac and skeletal muscle; Hypertrophy; Myofibril; Sarcomere

Indexed keywords

M PROTEIN;

CELL GROWTH; CELL SHAPE; CELL VOLUME; HEART MUSCLE; MUSCLE FIBRIL; MUSCLE FUNCTION; MUSCLE HYPERTROPHY; MUSCLE MASS; MUSCLE TONE; PRIORITY JOURNAL; PROTEIN ASSEMBLY; PROTEIN SYNTHESIS; REVIEW; SARCOMERE; SKELETAL MUSCLE;

EID: 0034055761     PISSN: 87507587     EISSN: None     Source Type: Journal    
DOI: 10.1152/jappl.2000.88.3.1127     Document Type: Review

References (34)

1. Barral, J. W., and H. F. Epstein. Protein machines and self assembly in muscle organization. Bioessays 21: 813-823, 1999.
2. Booth, F. W., and D. B. Thomason. Molecular and cellular adaptation of muscle in response to exercise: perspectives of various models. Physiol. Rev. 71: 541-585, 1991.
3. i and contractile activity. Am. J. Physiol. Cell Physiol. 271: C1447-C1456, 1996.
4. Dabiri, G. A., K. K. Turnacioglu, J. M. Sanger, and J. W. Sanger. Myofibrillogenesis visualized in living embryonic cardiomyocytes. Proc. Natl. Acad. Sci. USA 94: 9493-9498, 1997.
5. Dix, D. J., and B. R. Eisenberg. Myosin mRNA accumulation and myofibrillogenesis at the myotendinous junction of stretched muscle fibers. J. Cell Biol. 111: 1885-1894, 1990.
6. Dlugosz, A. A., P. B. Antin, V. T. Nachmias, and H. Holtzer. The relationship between stress fiber-like structures and nascent myofibrils in cultured cardiac myocytes. J. Cell Biol. 99: 2268-2278, 1984.
7. Ehler, E., B. M. Rothen, S. P. Hammerle, M. Komiyama, and J. C. Perriard. Myofibrillogenesis in the developing chicken heart: assembly of Z-disk, M-line and the thick filaments. J. Cell. Sci. 112: 1529-1539, 1999.
8. Eisenberg, B. R., P. H. Goldspink, and M. P. Wenderoth. Distribution of myosin heavy chain mRNA in normal and hyperthyroid heart. J. Mol. Cell Cardiol. 23: 287-296, 1991.
9. Eisenberg, B. R., and S. Salmons. The reorganization of subcellular structure in muscle undergoing fast-to-slow type transformation. A stereological study. Cell Tissue Res. 220: 449-71, 1981.
10. Epstein, H. F., and D. A. Fischman. Molecular analysis of protein assembly in muscle development. Science 251: 1039-1044, 1991.
11. Garlick, P. J. An analysis of errors in estimation of the rate of protein synthesis by constant infusion of a labelled amino acid. Biochem. J. 176: 402-405, 1978.
12. Goldspink, G. Changes in muscle mass and phenotype and the expression of autocrine and systemic growth factors by muscle in response to stretch and overload. J. Anat. 194: 323-334, 1999.
13. Goldspink, P. H., D. B. Thomason, and B. Russell. Beating affects the posttranscriptional regulation of α-myosin mRNA in cardiac cultures. Am. J. Physiol. Heart Circ. Physiol. 271: H2584-H2590, 1996.
14. Gray's Anatomy (38th ed.). Churchill Livingstone, 1995, chapt. 7, p. 737-785.
15. Gregorio, C. C., A. Weber, M. Bondad, C. R. Pennise, and V. M. Fowler. Requirement of point-end capping by tropomodulin to maintain actin filament length in embryonic chick cardiac myocytes. Nature 377: 83-86, 1995.
16. Huang, S., C. S. Chen, and D. E. Ingber. Control of cyclin D1, p27(Kip1), and cell cycle progression in human capillary endothelial cells by cell shape and cytoskeletal tension. Mol. Biol. Cell 9: 3179-3193, 1998.
17. Hunter, J. J., and K. R Chien. Mechanisms of disease signaling pathways for cardiac hypertrophy and failure. N. Engl. J. Med. 341: 1276-1283, 1999.
18. Loughna, P. T., S. Izumo, G. Goldspink, and B. Nadal-Ginard. Disuse and passive stretch cause rapid alterations in expression of developmental and adult contractile protein genes in skeletal muscle. Development 109: 217-223, 1990.
19. Martin, A. F. Turnover of cardiac troponin subunits. Kinetic evidence for a precursor pool of troponin-I. J. Biol. Chem. 256: 964-968, 1981.
20. Michele, D. E., F. P. Albayya, and J. M. Metzger. Thin filament protein dynamics in fully differentiated adult cardiac myocytes: toward a model of sarcomere maintenance. J. Cell. Biol. 145: 1483-1495, 1999.
21. Morkin, E., Y. Yazaki, T. Katagiri, and P. J. Laraia. Comparison of the synthesis of the light and heavy chains of adult skeletal myosin. Biochim. Biophys. Acta 324: 420-429, 1973.
22. Perhonen, M., W. W. Sharp, and B. Russell. Microtubules are needed for cytoplasmic transport of α-myosin heavy chain mRNA in rat neonatal cardiac myocytes. J. Mol. Cell. Cardiol. 30: 1713-1722, 1998.
23. Pette, D., and G. Vrbova. What does chronic electrical stimulation teach us about muscle plasticity? Muscle Nerve 22: 666-677, 1999.
24. Rhee, D., J. M. Sanger, and J. W. Sanger. The premyofibril: evidence for its role in myofibrillogenesis. Cell. Motil. Cytoskeleton 28: 1-24, 1994.
25. Russell, B., and D. J. Dix. Mechanisms for intracellular distribution of mRNA: in situ hybridization studies in muscle. Am. J. Physiol. Cell Physiol. 262: C1-C6, 1992.
26. Russell, B., M. P. Wenderoth, and P. H. Goldspink. Remodeling of myofibrils: subcellular myosin heavy chain protein and mRNA distribution. Am. J. Physiol. Regulatory Integrative Comp. Physiol. 262: R339-R345, 1992.
27. Samarel, A. M., M. L. Spragia, V. Maloney, S. A. Kamal, and G. L. Engelmann. Contractile arrest accelerates myosin heavy chain degradation in neonatal rat heart cells. Am. J. Physiol. Cell Physiol. 263: C642-C652, 1992.
28. Schultheiss, T., Z. X. Lin, M. H. Lu, J. Murray, D. A. Fischman, K. Weber, T. Masaki, M. Imamura, and H. Holtzer. Differential distribution of subsets of myofibrillar proteins in cardiac nonstriated and striated myofibrils. J. Cell. Biol. 110: 1159-1172, 1990.
29. Simpson, D. G., M. Majeski, T. K Borg, and L. Terracio. Regulation of cardiac myocytes protein turnover and myofibrillar structure in vitro by specific directions of stretch. Circ. Res. 85: 59-69, 1999.
30. Simpson, D. G., W. W. Sharp, T. K. Borg, R. L. Price, L. Terracio, and A. M. Samarel. Mechanical regulation of cardiac myocyte protein turnover and myofibrillar structure. Am. J. Physiol. Cell Physiol. 270: C1075-C1087, 1996.
31. Solaro, R. J., and H. M. Rarick. Troponin and tropomyosin: proteins that switch on and tune in the activity of cardiac myofilaments. Circ. Res. 83: 471-480, 1998.
32. Wenderoth, M. P., and B. R. Eisenberg. Incorporation of nascent myosin heavy chains into thick filaments of cardiac myocytes in thyroid-treated rabbits. J. Cell. Biol. 105: 2771-2780, 1987.
33. Williams, P., P. Watt, V. Bicik, and G. Goldspink. Effect of stretch combined with electrical stimulation on the type of sarcomeres produced at the ends of muscle fibers. Exp. Neurol. 93: 500-509, 1986.
34. Winegrad, S. Cardiac myosin binding protein C. Circ. Res. 84: 1117-1126, 1999.