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. 1987 Dec 1;105(6):2771–2780. doi: 10.1083/jcb.105.6.2771

Incorporation of nascent myosin heavy chains into thick filaments of cardiac myocytes in thyroid-treated rabbits

PMCID: PMC2114681  PMID: 3320054

Abstract

A monoclonal antibody (mAb 37) specific for alpha-myosin heavy chain (alpha-MHC) is used to follow the spatial and temporal incorporation of alpha-MHC into rabbit left ventricular myocytes. The expression of the two adult cardiac MHC genes, alpha and beta, is regulated by manipulating the thyroid hormone level of the animal. 10 wk on a propylthiouracil diet down-regulates expression of alpha-MHC to near 0%. alpha-MHC gene expression is up-regulated by injecting L- triiodothyronine (100 micrograms/kg per d) for 1-4 d. This protocol provides a means by which to follow the redistribution pattern of alpha- MHC within the myocyte in vivo. A uniform distribution of immunofluorescent signal is seen within every myocyte throughout the left ventricle. Ultracryomicrotomy without fixation is used to obtain sections for immunogold-electron microscopy. To quantify the immunogold method the density of gold-labeled antibody per unit of area tissue is determined for various regions of the sarcomere. Tissue from normal and 2-wk baby has a uniform distribution of gold density along the length of the A band. The average gold density of the A band increases with days of thyroid injection from 38 +/- 4 grains/micron 2 (n = 2 animals) (mean +/- SE) at day 1 to 182 +/- 59 grains (n = 2 animals) at day 4. There is a nonuniform incorporation of the newly synthesized alpha-MHC within the A band of thyroid-treated animals since 50% more of the alpha-MHC is found at the end of the A band while the center of the A band has 40% less than the average alpha-MHC content (grains/micron 2, n = 7 animals). These results support a thick filament assembly model that allows every myosin in a thick filament to be exchanged with new myosin. However, in the intact functioning myocyte, there is greater exchange of new myosin at the ends than in the central region of the thick filament.

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Selected References

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  1. Amato P. A., Taylor D. L. Probing the mechanism of incorporation of fluorescently labeled actin into stress fibers. J Cell Biol. 1986 Mar;102(3):1074–1084. doi: 10.1083/jcb.102.3.1074. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Chizzonite R. A., Everett A. W., Clark W. A., Jakovcic S., Rabinowitz M., Zak R. Isolation and characterization of two molecular variants of myosin heavy chain from rabbit ventricle. Change in their content during normal growth and after treatment with thyroid hormone. J Biol Chem. 1982 Feb 25;257(4):2056–2065. [PubMed] [Google Scholar]
  3. Crisona N. J., Strohman R. C. Inhibition of contraction of cultured muscle fibers results in increased turnover of myofibrillar proteins but not of intermediate-filament proteins. J Cell Biol. 1983 Mar;96(3):684–692. doi: 10.1083/jcb.96.3.684. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Davis J. S. A model for length-regulation in thick filaments of vertebrate skeletal myosin. Biophys J. 1986 Sep;50(3):417–422. doi: 10.1016/S0006-3495(86)83477-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Dlugosz A. A., Antin P. B., Nachmias V. T., Holtzer H. The relationship between stress fiber-like structures and nascent myofibrils in cultured cardiac myocytes. J Cell Biol. 1984 Dec;99(6):2268–2278. doi: 10.1083/jcb.99.6.2268. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Eisenberg B. R., Edwards J. A., Zak R. Transmural distribution of isomyosin in rabbit ventricle during maturation examined by immunofluorescence and staining for calcium-activated adenosine triphosphatase. Circ Res. 1985 Apr;56(4):548–555. doi: 10.1161/01.res.56.4.548. [DOI] [PubMed] [Google Scholar]
  7. Eppenberger H. M., Perriard J. C., Rosenberg U. B., Strehler E. E. The Mr 165,000 M-protein myomesin: a specific protein of cross-striated muscle cells. J Cell Biol. 1981 May;89(2):185–193. doi: 10.1083/jcb.89.2.185. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Everett A. W., Sinha A. M., Umeda P. K., Jakovcic S., Rabinowitz M., Zak R. Regulation of myosin synthesis by thyroid hormone: relative change in the alpha- and beta-myosin heavy chain mRNA levels in rabbit heart. Biochemistry. 1984 Apr 10;23(8):1596–1599. doi: 10.1021/bi00303a002. [DOI] [PubMed] [Google Scholar]
  9. Gauthier G. F., Lowey S. Distribution of myosin isoenzymes among skeletal muscle fiber types. J Cell Biol. 1979 Apr;81(1):10–25. doi: 10.1083/jcb.81.1.10. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Harrington W. F., Rodgers M. E. Myosin. Annu Rev Biochem. 1984;53:35–73. doi: 10.1146/annurev.bi.53.070184.000343. [DOI] [PubMed] [Google Scholar]
  11. Higuchi H., Ishiwata S. Disassembly kinetics of thick filaments in rabbit skeletal muscle fibers. Effects of ionic strength, Ca2+ concentration, pH, temperature, and cross-bridges on the stability of thick filament structure. Biophys J. 1985 Mar;47(3):267–275. doi: 10.1016/S0006-3495(85)83916-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Hoh J. F., McGrath P. A., Hale P. T. Electrophoretic analysis of multiple forms of rat cardiac myosin: effects of hypophysectomy and thyroxine replacement. J Mol Cell Cardiol. 1978 Nov;10(11):1053–1076. doi: 10.1016/0022-2828(78)90401-7. [DOI] [PubMed] [Google Scholar]
  13. Isaacs W. B., Fulton A. B. Cotranslational assembly of myosin heavy chain in developing cultured skeletal muscle. Proc Natl Acad Sci U S A. 1987 Sep;84(17):6174–6178. doi: 10.1073/pnas.84.17.6174. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Ishiwata S., Muramatsu K., Higuchi H. Disassembly from both ends of thick filaments in rabbit skeletal muscle fibers. An optical diffraction study. Biophys J. 1985 Mar;47(3):257–266. doi: 10.1016/S0006-3495(85)83915-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Kovacs L., Rios E., Schneider M. F. Measurement and modification of free calcium transients in frog skeletal muscle fibres by a metallochromic indicator dye. J Physiol. 1983 Oct;343:161–196. doi: 10.1113/jphysiol.1983.sp014887. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Kuczmarski E. R., Rosenbaum J. L. Chick brain actin and myosin. Isolation and characterization. J Cell Biol. 1979 Feb;80(2):341–355. doi: 10.1083/jcb.80.2.341. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Kuettel M. R., Squinto S. P., Kwast-Welfeld J., Schwoch G., Schweppe J. S., Jungmann R. A. Localization of nuclear subunits of cyclic AMP-dependent protein kinase by the immunocolloidal gold method. J Cell Biol. 1985 Sep;101(3):965–975. doi: 10.1083/jcb.101.3.965. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Larson P. F., Fulthorpe J. J., Hudgson P. The alignment of polysomes along myosin filaments in developing myofibrils. J Anat. 1973 Dec;116(Pt 3):327–334. [PMC free article] [PubMed] [Google Scholar]
  19. Lawrence J. B., Singer R. H. Intracellular localization of messenger RNAs for cytoskeletal proteins. Cell. 1986 May 9;45(3):407–415. doi: 10.1016/0092-8674(86)90326-0. [DOI] [PubMed] [Google Scholar]
  20. Maruyama K., Matsubara S., Natori R., Nonomura Y., Kimura S. Connectin, an elastic protein of muscle. Characterization and Function. J Biochem. 1977 Aug;82(2):317–337. [PubMed] [Google Scholar]
  21. Maruyama K., Yoshioka T., Higuchi H., Ohashi K., Kimura S., Natori R. Connectin filaments link thick filaments and Z lines in frog skeletal muscle as revealed by immunoelectron microscopy. J Cell Biol. 1985 Dec;101(6):2167–2172. doi: 10.1083/jcb.101.6.2167. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Maw M. C., Rowe A. J. The reconstruction of myosin filaments in rabbit psoas muscle from solubilized myosin. J Muscle Res Cell Motil. 1986 Apr;7(2):97–109. doi: 10.1007/BF01753410. [DOI] [PubMed] [Google Scholar]
  23. McLean I. W., Nakane P. K. Periodate-lysine-paraformaldehyde fixative. A new fixation for immunoelectron microscopy. J Histochem Cytochem. 1974 Dec;22(12):1077–1083. doi: 10.1177/22.12.1077. [DOI] [PubMed] [Google Scholar]
  24. Morkin E., Kimata S., Skillman J. J. Myosin synthesis and degradation during development of cardiac hypertrophy in the rabbit. Circ Res. 1972 Jun;30(6):690–702. doi: 10.1161/01.res.30.6.690. [DOI] [PubMed] [Google Scholar]
  25. Nachmias V. Filament formation by purified Physarum myosin. Proc Natl Acad Sci U S A. 1972 Aug;69(8):2011–2014. doi: 10.1073/pnas.69.8.2011. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Offer G., Moos C., Starr R. A new protein of the thick filaments of vertebrate skeletal myofibrils. Extractions, purification and characterization. J Mol Biol. 1973 Mar 15;74(4):653–676. doi: 10.1016/0022-2836(73)90055-7. [DOI] [PubMed] [Google Scholar]
  27. Pardee J. D., Simpson P. A., Stryer L., Spudich J. A. Actin filaments undergo limited subunit exchange in physiological salt conditions. J Cell Biol. 1982 Aug;94(2):316–324. doi: 10.1083/jcb.94.2.316. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Pearse A. G., Polak J. M. Bifunctional reagents as vapour- and liquid-phase fixatives for immunohistochemistry. Histochem J. 1975 Mar;7(2):179–186. doi: 10.1007/BF01004561. [DOI] [PubMed] [Google Scholar]
  29. Pollard T. D. Electron microscopy of synthetic myosin filaments. Evidence for cross-bridge. Flexibility and copolymer formation. J Cell Biol. 1975 Oct;67(1):93–104. doi: 10.1083/jcb.67.1.93. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Reisler E., Cheung P., Borochov N., Lake J. A. Monomers, dimers, and minifilaments of vertebrate skeletal myosin in the presence of sodium pyrophosphate. Biochemistry. 1986 Jan 28;25(2):326–332. doi: 10.1021/bi00350a007. [DOI] [PubMed] [Google Scholar]
  31. Roberts I. M. Tungsten coating--a method of improving glass microtome knives for cutting ultrathin sections. J Microsc. 1975 Jan;103(1):113–119. doi: 10.1111/j.1365-2818.1975.tb04542.x. [DOI] [PubMed] [Google Scholar]
  32. Saad A. D., Fischman D. A., Pardee J. D. Fluorescence energy transfer studies of Myosin thick filament assembly. Biophys J. 1986 Jan;49(1):140–142. doi: 10.1016/S0006-3495(86)83626-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Saad A. D., Pardee J. D., Fischman D. A. Dynamic exchange of myosin molecules between thick filaments. Proc Natl Acad Sci U S A. 1986 Dec;83(24):9483–9487. doi: 10.1073/pnas.83.24.9483. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Samuel J. L., Rappaport L., Mercadier J. J., Lompre A. M., Sartore S., Triban C., Schiaffino S., Schwartz K. Distribution of myosin isozymes within single cardiac cells. An immunohistochemical study. Circ Res. 1983 Feb;52(2):200–209. doi: 10.1161/01.res.52.2.200. [DOI] [PubMed] [Google Scholar]
  35. Sharp N. A., Neel D. S., Parsons R. L. Influence of thyroid hormone levels on the electrical and mechanical properties of rabbit papillary muscle. J Mol Cell Cardiol. 1985 Feb;17(2):119–132. doi: 10.1016/s0022-2828(85)80015-8. [DOI] [PubMed] [Google Scholar]
  36. Sjöström M., Squire J. M. Fine structure of the A-band in cryo-sections. The structure of the A-band of human skeletal muscle fibres from ultra-thin cryo-sections negatively stained. J Mol Biol. 1977 Jan 5;109(1):49–68. doi: 10.1016/s0022-2836(77)80045-4. [DOI] [PubMed] [Google Scholar]
  37. Starr R., Almond R., Offer G. Location of C-protein, H-protein and X-protein in rabbit skeletal muscle fibre types. J Muscle Res Cell Motil. 1985 Apr;6(2):227–256. doi: 10.1007/BF00713063. [DOI] [PubMed] [Google Scholar]
  38. Tokuyasu K. T. Application of cryoultramicrotomy to immunocytochemistry. J Microsc. 1986 Aug;143(Pt 2):139–149. doi: 10.1111/j.1365-2818.1986.tb02772.x. [DOI] [PubMed] [Google Scholar]
  39. Tokuyasu K. T., Dutton A. H., Geiger B., Singer S. J. Ultrastructure of chicken cardiac muscle as studied by double immunolabeling in electron microscopy. Proc Natl Acad Sci U S A. 1981 Dec;78(12):7619–7623. doi: 10.1073/pnas.78.12.7619. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Wachsberger P. R., Pepe F. A. Interaction between vertebrate skeletal and uterine muscle myosins and light meromyosins. J Cell Biol. 1980 Apr;85(1):33–41. doi: 10.1083/jcb.85.1.33. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Wang K., Ramirez-Mitchell R. A network of transverse and longitudinal intermediate filaments is associated with sarcomeres of adult vertebrate skeletal muscle. J Cell Biol. 1983 Feb;96(2):562–570. doi: 10.1083/jcb.96.2.562. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Willingham M. C., Yamada S. S. Development of a new primary fixative for electron microscopic immunocytochemical localization of intracellular antigens in cultured cells. J Histochem Cytochem. 1979 May;27(5):947–960. doi: 10.1177/27.5.90071. [DOI] [PubMed] [Google Scholar]
  43. Zak R., Chizzonite R. A., Everett A. W., Clark W. A. Study of ventricular isomyosins during normal and thyroid hormone induced cardiac growth. J Mol Cell Cardiol. 1982 Sep;14 (Suppl 3):111–117. doi: 10.1016/0022-2828(82)90138-9. [DOI] [PubMed] [Google Scholar]

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