Literature DB >> 6376158

Structural change of myofibrils during mitosis of newt embryonic myocardial cells in culture.

H Kaneko, M Okamoto, K Goshima.   

Abstract

Newt embryonic myocardial cells can undergo mitosis in culture. The successive changes in the striation pattern of sarcomeres of myofibrils during mitosis were studied by polarization microscopy without fixing or killing the cells. Birefringence of well-organized striation patterns, i.e., bright A-bands and dark I-bands, was clearly visible in interphase cells and did not show any detectable changes during incubation for 3 h or more. Electron microscopy showed the presence of well-organized myofibrils with Z-bands in these interphase cells. When myocardial cells entered the mitotic stage, the birefringence of striation pattern of their myofibrils gradually changed with the pattern in small parts of the myofibrils gradually becoming indistinct (called 'indistinct striation' in this paper). These indistinct regions increased in size during the mitotic stage. In addition, in some regions of the indistinct striation, the birefringence of sarcomeres gradually decreased and finally disappeared (called 'disappearance of sarcomeres' in this paper). No myocardial cells underwent mitosis without these disruptive changes of the myofibril striation patterns. In the post-mitotic stage, the well-organized striation of the myofibrils reappeared. Electron microscopy showed disorganized sarcomeres without Z-bands in the regions of indistinct striation, and no well-organized myofibrils in the regions where the sarcomeres had disappeared. Thus the well-organized myofibrils with Z-bands became transiently disorganized at least in some parts, during mitosis. They were then reorganized into daughter myocardial cells.

Mesh:

Year:  1984        PMID: 6376158     DOI: 10.1016/0014-4827(84)90615-3

Source DB:  PubMed          Journal:  Exp Cell Res        ISSN: 0014-4827            Impact factor:   3.905


  8 in total

1.  How to build a myofibril.

Authors:  Joseph W Sanger; Songman Kang; Cornelia C Siebrands; Nancy Freeman; Aiping Du; Jushuo Wang; Andrea L Stout; Jean M Sanger
Journal:  J Muscle Res Cell Motil       Date:  2005       Impact factor: 2.698

2.  Disruption of microfilament organization in living nonmuscle cells by microinjection of plasma vitamin D-binding protein or DNase I.

Authors:  J M Sanger; G Dabiri; B Mittal; M A Kowalski; J G Haddad; J W Sanger
Journal:  Proc Natl Acad Sci U S A       Date:  1990-07       Impact factor: 11.205

3.  Cardiac myofibrillogenesis inside intact embryonic hearts.

Authors:  Aiping Du; Jean M Sanger; Joseph W Sanger
Journal:  Dev Biol       Date:  2008-03-20       Impact factor: 3.582

4.  A primary cell culture model for defective cardiac myofibrillogenesis in Mexican axolotl embryos.

Authors:  R W Zajdel; Y Zhu; M E Fransen; L F Lemanski
Journal:  In Vitro Cell Dev Biol Anim       Date:  1997-10       Impact factor: 2.416

5.  Multiple influences of blood flow on cardiomyocyte hypertrophy in the embryonic zebrafish heart.

Authors:  Yi-Fan Lin; Ian Swinburne; Deborah Yelon
Journal:  Dev Biol       Date:  2011-12-13       Impact factor: 3.582

6.  Phorbol esters selectively and reversibly inhibit a subset of myofibrillar genes responsible for the ongoing differentiation program of chick skeletal myotubes.

Authors:  J K Choi; S Holtzer; S A Chacko; Z X Lin; R K Hoffman; H Holtzer
Journal:  Mol Cell Biol       Date:  1991-09       Impact factor: 4.272

7.  Formation and alignment of Z lines in living chick myotubes microinjected with rhodamine-labeled alpha-actinin.

Authors:  N M McKenna; C S Johnson; Y L Wang
Journal:  J Cell Biol       Date:  1986-12       Impact factor: 10.539

8.  Differential response of myofibrillar and cytoskeletal proteins in cells treated with phorbol myristate acetate.

Authors:  Z X Lin; J Eshleman; C Grund; D A Fischman; T Masaki; W W Franke; H Holtzer
Journal:  J Cell Biol       Date:  1989-03       Impact factor: 10.539

  8 in total

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