Literature DB >> 2266168

Assembly of connectin (titin) in relation to myosin and alpha-actinin in cultured cardiac myocytes.

M Komiyama1, K Maruyama, Y Shimada.   

Abstract

By using polyclonal and monoclonal antibodies against connectin (titin) which stain the A-I junctional area and the A-band domain (polyclonal anti-connectin and monoclonal 4C9) and the I-band domain (monoclonal SM1), the developmental relationship of this elastic protein with sarcomeric proteins, especially and alpha-actin, was examined in embryonic chick cardiac myocytes in vitro under fluorescence microscopy. During premyofibril stages, I-Z-I proteins were detected first (alpha-actinin dots and diffuse actin [phalloidin and anti-troponin C] staining), and later in these areas connectin and myosin dots appeared with nearly identical distribution. Somewhat later, phalloidin-positive nonstriated fibrils were observed in a straight course. They were always reactive with antibodies against alpha-actinin and troponin C, but unreactive or only weakly reactive with anticonnectin and anti-myosin. Initially, alpha-actinin dots were aligned along these fibrils but did not form striations. As they aggregated to form Z-bands, connectin and myosin started to exhibit typical striation ('doublets' and A-bands, respectively). No difference in the staining pattern was observed with two kinds of monoclonal antibodies against different domains of connectin filaments (4C9 and SM1) at early phases. As myosin staining began to show clear A-bands, connectin epitopes became arranged in polarized positions. We conclude that primitive I-Z-I complexes appear prior to the assembly of connectin and myosin filaments and then connectin filaments, developing intimately and coordinately with myosin, become associated with the alpha-actinin lines. Thus it appears that the putative elastic protein connectin plays some role in integrating myosin filaments with the preexisting I-Z-I brushes. The occasional absence of connectin and A-bands between two Z-bands, beyond both of which clear sarcomeres have been formed, indicates that connectin is not a preformed scaffold of myofibrils on which sarcomeric proteins accumulate.

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Year:  1990        PMID: 2266168     DOI: 10.1007/bf01739762

Source DB:  PubMed          Journal:  J Muscle Res Cell Motil        ISSN: 0142-4319            Impact factor:   2.698


  25 in total

1.  The development of myofibrils in cultured muscle cells: a whole-mount and thin-section electron microscopic study.

Authors:  H B Peng; J J Wolosewick; P C Cheng
Journal:  Dev Biol       Date:  1981-11       Impact factor: 3.582

2.  The relationship between stress fiber-like structures and nascent myofibrils in cultured cardiac myocytes.

Authors:  A A Dlugosz; P B Antin; V T Nachmias; H Holtzer
Journal:  J Cell Biol       Date:  1984-12       Impact factor: 10.539

3.  Anti-connectin monoclonal antibodies that react with the unc-22 gene product bind dense bodies of Caenorhabditis (Nematode) bodywall muscle cells.

Authors:  A Matsuno; H Takaimo-Ohmuro; Y Itoh; T Matsuura; M Shibata; H Nakae; T Kaminuma; K Maruyama
Journal:  Tissue Cell       Date:  1989       Impact factor: 2.466

4.  Myofibril assembly is linked with vinculin, alpha-actinin, and cell-substrate contacts in embryonic cardiac myocytes in vitro.

Authors:  M Terai; M Komiyama; Y Shimada
Journal:  Cell Motil Cytoskeleton       Date:  1989

5.  Myogenesis in the mouse embryo: differential onset of expression of myogenic proteins and the involvement of titin in myofibril assembly.

Authors:  D O Fürst; M Osborn; K Weber
Journal:  J Cell Biol       Date:  1989-08       Impact factor: 10.539

6.  The positional stability of thick filaments in activated skeletal muscle depends on sarcomere length: evidence for the role of titin filaments.

Authors:  R Horowits; R J Podolsky
Journal:  J Cell Biol       Date:  1987-11       Impact factor: 10.539

7.  Connectin filaments in stretched skinned fibers of frog skeletal muscle.

Authors:  K Maruyama; H Sawada; S Kimura; K Ohashi; H Higuchi; Y Umazume
Journal:  J Cell Biol       Date:  1984-10       Impact factor: 10.539

8.  Connectin filaments link thick filaments and Z lines in frog skeletal muscle as revealed by immunoelectron microscopy.

Authors:  K Maruyama; T Yoshioka; H Higuchi; K Ohashi; S Kimura; R Natori
Journal:  J Cell Biol       Date:  1985-12       Impact factor: 10.539

9.  Titin and myosin, but not desmin, are linked during myofibrillogenesis in postmitotic mononucleated myoblasts.

Authors:  C S Hill; S Duran; Z X Lin; K Weber; H Holtzer
Journal:  J Cell Biol       Date:  1986-12       Impact factor: 10.539

10.  Differential expression and distribution of chicken skeletal- and smooth-muscle-type alpha-actinins during myogenesis in culture.

Authors:  T Endo; T Masaki
Journal:  J Cell Biol       Date:  1984-12       Impact factor: 10.539

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  11 in total

1.  Thick filament assembly occurs after the formation of a cytoskeletal scaffold.

Authors:  P F Van der Ven; E Ehler; J C Perriard; D O Fürst
Journal:  J Muscle Res Cell Motil       Date:  1999-08       Impact factor: 2.698

2.  Remodelling of adult cardiac muscle cells in culture: dynamic process of disorganization and reorganization of myofibrils.

Authors:  A C Nag; M L Lee; F H Sarkar
Journal:  J Muscle Res Cell Motil       Date:  1996-06       Impact factor: 2.698

3.  Incorporation of microinjected biotin-labelled actin into nascent myofibrils of cardiac myocytes: an immunoelectron microscopic study.

Authors:  K Kouchi; H Takahashi; Y Shimada
Journal:  J Muscle Res Cell Motil       Date:  1993-06       Impact factor: 2.698

4.  The distribution of desmin and titin in normal and dystrophic human muscle.

Authors:  M J Cullen; J J Fulthorpe; J B Harris
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

5.  Spatial relationship of nebulin relative to other myofibrillar proteins during myogenesis in embryonic chick skeletal muscle cells in vitro.

Authors:  M Komiyama; Z H Zhou; K Maruyama; Y Shimada
Journal:  J Muscle Res Cell Motil       Date:  1992-02       Impact factor: 2.698

6.  Dynamics of actin and alpha-actinin in nascent myofibrils and stress fibers.

Authors:  F Hasebe-Kishi; Y Shimada
Journal:  J Muscle Res Cell Motil       Date:  2000       Impact factor: 2.698

7.  Exon- and contraction-dependent functions of titin in sarcomere assembly.

Authors:  Yu-Huan Shih; Alexey V Dvornikov; Ping Zhu; Xiao Ma; Maengjo Kim; Yonghe Ding; Xiaolei Xu
Journal:  Development       Date:  2016-11-11       Impact factor: 6.868

8.  The fate of desmin and titin during the degeneration and regeneration of the soleus muscle of the rat.

Authors:  R Vater; M J Cullen; J B Harris
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

9.  CUG-BP, Elav-like family member 1 (CELF1) is required for normal myofibrillogenesis, morphogenesis, and contractile function in the embryonic heart.

Authors:  Yotam Blech-Hermoni; Connor B Sullivan; Michael W Jenkins; Oliver Wessely; Andrea N Ladd
Journal:  Dev Dyn       Date:  2016-05-31       Impact factor: 3.780

10.  Cytoplasmic body myopathy: familial cases with accumulation of desmin and dystrophin. An immunohistochemical, immunoelectron microscopic and biochemical study.

Authors:  A Caron; F Viader; B Lechevalier; F Chapon
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088

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