Abstract
Our initial attempts to immunolabel intact myocardial walls of 4-12 somite stage chick embryos were hindered by the presence of the cardiac jelly that covers the inner myocardial wall surface and prevents the access of antibodies to that surface. We overcame this difficulty by treating the specimens with hyaluronidase, which made the cardiac jelly permeable to the antibodies. An additional nonionic detergent treatment made the two or more cell layers of the myocardial wall accessible to the antibodies from both surfaces of the wall. Specimens treated in this manner were fluorescently labeled with antibodies to titin, myosin, or actin or with NBD-phallacidin for F-actin and examined as whole mount preparations or cut into semithin sections after resin embedding. These preparations and sections revealed that titin, a putative scaffolding protein of sarcomeres, is present in a punctate state and also in a diffuse form throughout the cytoplasm of cardiac myocytes in the premyofibril stages (4-7 somite stages) as well as in the early stages of myofibril formation. We interpreted the punctate and diffuse states to represent an aggregated state of several titin molecules and a dispersed state of individual titin molecules, respectively. In the 4-7 somite cardiac primodia, myosin and actin show only a uniform labeling throughout the cytoplasm of the myocytes. These observations are in contrast to a previous report that titin and myosin are tightly linked during in vitro skeletal myofibrillogenesis (Hill, C. S., S. Duran, Z. Ling, K. Weber, and H. Holtzer, 1986, J. Cell Biol., 103:2185-2196). In the 8-11 somite stage hearts, the number of individual titin spots rapidly reduces, while the number of myofibrils with periodically aligned titin spots increases, which strongly suggests that the titin spots are incorporated into the newly arising myofibrils. Titin spots were seen as doublets only after titin spots were incorporated into the first myofibrils. However, the fact that the distance between the components of the narrowest doublet was close to the resolution limit of the light microscope left open the possibility that undiscernible doublets of submicroscopic separations might exist in the premyofibril stages. The myosin labeling revealed the sarcomeric periodicity in an earlier stage of myofibril development than the F- actin labeling. In addition, we made two morphogenic observations.(ABSTRACT TRUNCATED AT 400 WORDS)
Full Text
The Full Text of this article is available as a PDF (6.8 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- 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]
- Fujii S., Hirota A., Kamino K. Optical indications of pace-maker potential and rhythm generation in early embryonic chick heart. J Physiol. 1981 Mar;312:253–263. doi: 10.1113/jphysiol.1981.sp013627. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gruen L. C., King N. L., Kurth L., McKenzie L. J. Studies on the structure of connectin in muscle. Int J Pept Protein Res. 1982 Nov;20(5):401–407. doi: 10.1111/j.1399-3011.1982.tb03059.x. [DOI] [PubMed] [Google Scholar]
- Hill C. S., Duran S., Lin Z. X., Weber K., Holtzer H. Titin and myosin, but not desmin, are linked during myofibrillogenesis in postmitotic mononucleated myoblasts. J Cell Biol. 1986 Dec;103(6 Pt 1):2185–2196. doi: 10.1083/jcb.103.6.2185. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hill C., Weber K. Monoclonal antibodies distinguish titins from heart and skeletal muscle. J Cell Biol. 1986 Mar;102(3):1099–1108. doi: 10.1083/jcb.102.3.1099. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hiruma T., Hirakow R. An ultrastructural topographical study on myofibrillogenesis in the heart of the chick embryo during pulsation onset period. Anat Embryol (Berl) 1985;172(3):325–329. doi: 10.1007/BF00318980. [DOI] [PubMed] [Google Scholar]
- Jorgensen A. O., Bashir R. Temporal appearance and distribution of the Ca2+ + Mg2+ ATPase of the sarcoplasmic reticulum in developing chick myocardium as determined by immunofluorescence labeling. Dev Biol. 1984 Nov;106(1):156–165. doi: 10.1016/0012-1606(84)90071-x. [DOI] [PubMed] [Google Scholar]
- KIELLEY W. W., HARRINGTON W. F. A model for the myosin molecule. Biochim Biophys Acta. 1960 Jul 15;41:401–421. doi: 10.1016/0006-3002(60)90037-8. [DOI] [PubMed] [Google Scholar]
- Karr T. L., Alberts B. M. Organization of the cytoskeleton in early Drosophila embryos. J Cell Biol. 1986 Apr;102(4):1494–1509. doi: 10.1083/jcb.102.4.1494. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
- Lim S. S., Woodroofe M. N., Lemanski L. F. An analysis of contractile proteins in developing chick heart by SDS polyacrylamide gel electrophoresis and electron microscopy. J Embryol Exp Morphol. 1983 Oct;77:1–14. [PubMed] [Google Scholar]
- Manasek F. J. Embryonic development of the heart. I. A light and electron microscopic study of myocardial development in the early chick embryo. J Morphol. 1968 Jul;125(3):329–365. doi: 10.1002/jmor.1051250306. [DOI] [PubMed] [Google Scholar]
- Manasek F. J. Histogenesis of the embryonic myocardium. Am J Cardiol. 1970 Feb;25(2):149–168. doi: 10.1016/0002-9149(70)90576-x. [DOI] [PubMed] [Google Scholar]
- Markwald R. R. Distribution and relationship of precursor Z material to organizing myofibrillar bundles in embryonic rat and hamster ventricular myocytes. J Mol Cell Cardiol. 1973 Aug;5(4):341–350. doi: 10.1016/0022-2828(73)90026-6. [DOI] [PubMed] [Google Scholar]
- Maruyama K., Kimura S., Yoshidomi H., Sawada H., Kikuchi M. Molecular size and shape of beta-connectin, an elastic protein of striated muscle. J Biochem. 1984 May;95(5):1423–1433. doi: 10.1093/oxfordjournals.jbchem.a134750. [DOI] [PubMed] [Google Scholar]
- 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]
- Pardee J. D., Spudich J. A. Purification of muscle actin. Methods Cell Biol. 1982;24:271–289. doi: 10.1016/s0091-679x(08)60661-5. [DOI] [PubMed] [Google Scholar]
- Peng H. B., Wolosewick J. J., Cheng P. C. The development of myofibrils in cultured muscle cells: a whole-mount and thin-section electron microscopic study. Dev Biol. 1981 Nov;88(1):121–136. doi: 10.1016/0012-1606(81)90224-4. [DOI] [PubMed] [Google Scholar]
- Rieder C. L., Bowser S. S. Correlative immunofluorescence and electron microscopy on the same section of epon-embedded material. J Histochem Cytochem. 1985 Feb;33(2):165–171. doi: 10.1177/33.2.3881520. [DOI] [PubMed] [Google Scholar]
- Rumyantsev P. P. Interrelations of the proliferation and differentiation processes during cardiact myogenesis and regeneration. Int Rev Cytol. 1977;51:186–273. [PubMed] [Google Scholar]
- Sanger J. M., Mittal B., Pochapin M. B., Sanger J. W. Myofibrillogenesis in living cells microinjected with fluorescently labeled alpha-actinin. J Cell Biol. 1986 Jun;102(6):2053–2066. doi: 10.1083/jcb.102.6.2053. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sissman N. J. Developmental landmarks in cardiac morphogenesis: comparative chronology. Am J Cardiol. 1970 Feb;25(2):141–148. doi: 10.1016/0002-9149(70)90575-8. [DOI] [PubMed] [Google Scholar]
- 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]
- Tokuyasu K. T., Maher P. A., Singer S. J. Distributions of vimentin and desmin in developing chick myotubes in vivo. I. Immunofluorescence study. J Cell Biol. 1984 Jun;98(6):1961–1972. doi: 10.1083/jcb.98.6.1961. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Towbin H., Staehelin T., Gordon J. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proc Natl Acad Sci U S A. 1979 Sep;76(9):4350–4354. doi: 10.1073/pnas.76.9.4350. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Trinick J., Knight P., Whiting A. Purification and properties of native titin. J Mol Biol. 1984 Dec 5;180(2):331–356. doi: 10.1016/s0022-2836(84)80007-8. [DOI] [PubMed] [Google Scholar]
- Virágh S., Challice C. E. Origin and differentiation of cardiac muscle cells in the mouse. J Ultrastruct Res. 1973 Jan;42(1):1–24. doi: 10.1016/s0022-5320(73)80002-4. [DOI] [PubMed] [Google Scholar]
- Wang K., McClure J., Tu A. Titin: major myofibrillar components of striated muscle. Proc Natl Acad Sci U S A. 1979 Aug;76(8):3698–3702. doi: 10.1073/pnas.76.8.3698. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wang K. Purification of titin and nebulin. Methods Enzymol. 1982;85(Pt B):264–274. doi: 10.1016/0076-6879(82)85025-8. [DOI] [PubMed] [Google Scholar]
- Wang K., Ramirez-Mitchell R., Palter D. Titin is an extraordinarily long, flexible, and slender myofibrillar protein. Proc Natl Acad Sci U S A. 1984 Jun;81(12):3685–3689. doi: 10.1073/pnas.81.12.3685. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wang K. Sarcomere-associated cytoskeletal lattices in striated muscle. Review and hypothesis. Cell Muscle Motil. 1985;6:315–369. doi: 10.1007/978-1-4757-4723-2_10. [DOI] [PubMed] [Google Scholar]
- Wang S. M., Greaser M. L. Immunocytochemical studies using a monoclonal antibody to bovine cardiac titin on intact and extracted myofibrils. J Muscle Res Cell Motil. 1985 Jun;6(3):293–312. doi: 10.1007/BF00713171. [DOI] [PubMed] [Google Scholar]
- Zhang Y., Shafiq S. A., Bader D. Detection of a ventricular-specific myosin heavy chain in adult and developing chicken heart. J Cell Biol. 1986 Apr;102(4):1480–1484. doi: 10.1083/jcb.102.4.1480. [DOI] [PMC free article] [PubMed] [Google Scholar]
