Literature DB >> 575268

Electron microscopic visualization of the filamentous reticulum in whole cultured presumptive chick myoblasts.

J Pudney, R H Singer.   

Abstract

This present study describes an experimental approach whereby subcellular 3-dimensional filamentous structures present within whole cells can be examined, using a conventional transmission electron microscope. This procedure uses cells which have been cultured on carbon-coated titanium grids, and treated with Triton X-100 to extract the soluble cytoplasm. Subsequent fixation and critical-point drying allows filamentous proteins to be easily visualized, due to the increase in contrast produced by removal of the ground cytoplasm. The high resolution obtainable in these preparations permitted an initial classification and description of the filamentous reticulum within cultured presumptive myoblasts. This reticulum is a continuum of filaments and cables, all elements of which appear to be interconnected. These morphological findings were then correlated with the biochemical identification of detergent-insoluble proteins, of which only actin, myosin, and, perhaps, intermediate filament and LETS protein are the major elements.

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Year:  1979        PMID: 575268     DOI: 10.1002/aja.1001560304

Source DB:  PubMed          Journal:  Am J Anat        ISSN: 0002-9106


  10 in total

1.  Myofibrillogenesis in vitro as seen with the scanning electron microscope.

Authors:  Y Isobe; Y Shimada
Journal:  Cell Tissue Res       Date:  1983       Impact factor: 5.249

2.  Alpha-spectrin in detergent-extracted whole-mount cytoskeletons of chicken embryo heart fibroblasts.

Authors:  R Sormunen
Journal:  Histochem J       Date:  1993-09

3.  Actin gene expression visualized in chicken muscle tissue culture by using in situ hybridization with a biotinated nucleotide analog.

Authors:  R H Singer; D C Ward
Journal:  Proc Natl Acad Sci U S A       Date:  1982-12       Impact factor: 11.205

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

Authors:  Y Isobe; Y Shimada
Journal:  Cell Tissue Res       Date:  1986       Impact factor: 5.249

5.  Ultrastructural visualization of cytoskeletal mRNAs and their associated proteins using double-label in situ hybridization.

Authors:  R H Singer; G L Langevin; J B Lawrence
Journal:  J Cell Biol       Date:  1989-06       Impact factor: 10.539

6.  Developmental reorganization of the skeletal framework and its surface lamina in fusing muscle cells.

Authors:  A B Fulton; J Prives; S R Farmer; S Penman
Journal:  J Cell Biol       Date:  1981-10       Impact factor: 10.539

7.  Mitotic architecture of the cell: the filament networks of the nucleus and cytoplasm.

Authors:  D G Capco; S Penman
Journal:  J Cell Biol       Date:  1983-03       Impact factor: 10.539

8.  Single mRNAs visualized by ultrastructural in situ hybridization are principally localized at actin filament intersections in fibroblasts.

Authors:  G J Bassell; C M Powers; K L Taneja; R H Singer
Journal:  J Cell Biol       Date:  1994-08       Impact factor: 10.539

9.  Poly(A) RNA codistribution with microfilaments: evaluation by in situ hybridization and quantitative digital imaging microscopy.

Authors:  K L Taneja; L M Lifshitz; F S Fay; R H Singer
Journal:  J Cell Biol       Date:  1992-12       Impact factor: 10.539

10.  Structural interaction of cytoskeletal components.

Authors:  M Schliwa; J van Blerkom
Journal:  J Cell Biol       Date:  1981-07       Impact factor: 10.539

  10 in total

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