ArticleCell and tissue research1986
Organization of filaments underneath the plasma membrane of developing chicken skeletal muscle cells in vitro revealed by the freeze-dry and rotary replica method.
Article in Cell and tissue research, 1986. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed, 23 citations in OpenAlex.
- Actin filament organization in aligned prefusion myoblasts.Journal of anatomy · 2004Article
- Visualization of the subsarcolemmal cytoskeleton network of mouse skeletal muscle cells by en face views and application to immunoelectron localization of dystrophin.Journal of muscle research and cell motility · 1995Article
- Three-dimensional distributions of desmin and vimentin in cultured hamster cardiomyocytes using the immunogold deep-etching replica technique.Histochemistry · 1994Article
- Immunofluorescent studies on Z-line-associated protein in cultured cardiomyocytes from neonatal hamsters.Cell and tissue research · 1993Article
- Size and localization of dystrophin molecule: immunoelectron microscopic and freeze etching studies of muscle plasma membranes of murine skeletal myofibers.Acta neuropathologica · 1993Article
- Immunocytochemical study of dystrophin in cultured mouse muscle cells by the quick-freezing and deep-etching method.The Histochemical journal · 1992Article
- Cytoskeletal filaments in embryonic chick myocardial cells as revealed by the quick-freeze deep-etch method combined with immunocytochemistry.Cell and tissue research · 1991Article
- Three-dimensional studies of the cytoskeleton of cultured hepatocytes: a quick-freezing and deep-etching study.Virchows Archiv. A, Pathological anatomy and histopathology · 1991Article
- Cytoskeletal injury and subsarcolemmal bleb formation in dog heart during in vitro total ischemia.The American journal of pathology · 1988Article
- Three-dimensional immunogold localization of alpha-actinin within the cytoskeletal networks of cultured cardiac muscle and nonmuscle cells.Proceedings of the National Academy of Sciences of the United States of America · 1988Article
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Authors and funding
2 authors at 1 institution in 1 country.
Funding
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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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