Literature DB >> 3698088

Organization of filaments underneath the plasma membrane of developing chicken skeletal muscle cells in vitro revealed by the freeze-dry and rotary replica method.

Y Isobe, Y Shimada.   

Abstract

Cytoskeletal organization and its association with plasma membranes in embryonic chick skeletal muscle cells in vitro was studied by the freeze-drying and rotary-shadowing method of physically ruptured cells. The cytoskeletal filaments underlying the plasma membranes were sparse in myogenic cells at the stage when cells exhibited great lipid fluidity in plasma membranes (fusion competent mononucleated myoblasts and recently fused young myotubes). Myotubes at more advanced stages of development possessed a highly interconnected dense filamentous network just underneath the cell membrane. This subsarcolemmal network was composed predominantly of 8-10 nm filaments; they were identified as actin filaments because of their decoration with myosin subfragment-1. Fine fibrils having a diameter of 3-5 nm were found on the protoplasmic surface of the plasmalemma at both the early and advanced stages of development. They were associated with the subsarcolemmal cytoskeletal filaments. Short 2-5 nm cross-linking filaments were occasionally seen between filaments in the subsarcolemmal network. We conclude that, although the subsarcolemmal cytoskeletal network contains many actin filaments, this domain appears to play some role in preserving the cell shape in the form of the membrane skeleton rather than membrane mobility.

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Year:  1986        PMID: 3698088     DOI: 10.1007/bf00218380

Source DB:  PubMed          Journal:  Cell Tissue Res        ISSN: 0302-766X            Impact factor:   5.249


  31 in total

1.  A metal impregnation method of biological specimens for scanning electron microscopy.

Authors:  T Murakami
Journal:  Arch Histol Jpn       Date:  1973-05

2.  Retention of differentiation potentialities during prolonged cultivation of myogenic cells.

Authors:  D Yaffe
Journal:  Proc Natl Acad Sci U S A       Date:  1968-10       Impact factor: 11.205

3.  Increased membrane fluidity precedes fusion of muscle cells.

Authors:  J Prives; M Shinitzky
Journal:  Nature       Date:  1977-08-25       Impact factor: 49.962

4.  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

5.  Fodrin is the general spectrin-like protein found in most cells whereas spectrin and the TW protein have a restricted distribution.

Authors:  J R Glenney; P Glenney
Journal:  Cell       Date:  1983-09       Impact factor: 41.582

6.  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

7.  The cytoplasmic filamentous network in cultured ovarian granulosa cells.

Authors:  B E Batten; J J Aalberg; E Anderson
Journal:  Cell       Date:  1980-10       Impact factor: 41.582

8.  Freeze-fracturing and deep-etching with the volatile cryoprotectant ethanol reveals true membrane surfaces of kidney structures.

Authors:  A Schiller; R Taugner
Journal:  Cell Tissue Res       Date:  1980       Impact factor: 5.249

9.  Filament organization revealed in platinum replicas of freeze-dried cytoskeletons.

Authors:  J E Heuser; M W Kirschner
Journal:  J Cell Biol       Date:  1980-07       Impact factor: 10.539

10.  Cytoskeletal network underlying the human erythrocyte membrane. Thin-section electron microscopy.

Authors:  S Tsukita; S Tsukita; H Ishikawa
Journal:  J Cell Biol       Date:  1980-06       Impact factor: 10.539

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  10 in total

1.  Actin filament organization in aligned prefusion myoblasts.

Authors:  Nathan T Swailes; Peter J Knight; Michelle Peckham
Journal:  J Anat       Date:  2004-11       Impact factor: 2.610

2.  Cytoskeletal filaments in embryonic chick myocardial cells as revealed by the quick-freeze deep-etch method combined with immunocytochemistry.

Authors:  Y Sugi; R Hirakow
Journal:  Cell Tissue Res       Date:  1991-03       Impact factor: 5.249

3.  Three-dimensional studies of the cytoskeleton of cultured hepatocytes: a quick-freezing and deep-etching study.

Authors:  S Ohno; Y Fujii
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1991

4.  Cytoskeletal injury and subsarcolemmal bleb formation in dog heart during in vitro total ischemia.

Authors:  M D Sage; R B Jennings
Journal:  Am J Pathol       Date:  1988-11       Impact factor: 4.307

5.  Three-dimensional immunogold localization of alpha-actinin within the cytoskeletal networks of cultured cardiac muscle and nonmuscle cells.

Authors:  Y Isobe; F D Warner; L F Lemanski
Journal:  Proc Natl Acad Sci U S A       Date:  1988-09       Impact factor: 11.205

6.  Immunofluorescent studies on Z-line-associated protein in cultured cardiomyocytes from neonatal hamsters.

Authors:  H E Osinska; L F Lemanski
Journal:  Cell Tissue Res       Date:  1993-01       Impact factor: 5.249

7.  Visualization of the subsarcolemmal cytoskeleton network of mouse skeletal muscle cells by en face views and application to immunoelectron localization of dystrophin.

Authors:  C Berthier; J Amsellem; S Blaineau
Journal:  J Muscle Res Cell Motil       Date:  1995-10       Impact factor: 2.698

8.  Size and localization of dystrophin molecule: immunoelectron microscopic and freeze etching studies of muscle plasma membranes of murine skeletal myofibers.

Authors:  Y Wakayama; S Shibuya; T Jimi; A Takeda; H Oniki
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088

9.  Three-dimensional distributions of desmin and vimentin in cultured hamster cardiomyocytes using the immunogold deep-etching replica technique.

Authors:  Y Isobe; M Nakatsugawa; G R Hou; L F Lemanski
Journal:  Histochemistry       Date:  1994-03

10.  Immunocytochemical study of dystrophin in cultured mouse muscle cells by the quick-freezing and deep-etching method.

Authors:  Y C Park-Matsumoto; S Ohno; T Baba; T Kobayashi; H Tsukagoshi
Journal:  Histochem J       Date:  1992-06
  10 in total

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