Literature DB >> 7193921

Intracellular filament bundles in whole mounts of chick and human myoblasts extracted with triton X-100.

J Pudney, R H Singer.   

Abstract

The method of Triton X-100 extraction and critical point drying of whole mounts of cultured chick and human myoblasts was used to study the presence of intracellular bundles of filaments within these cells. Observation by means of transmission and scanning electron microscopy demonstrated a complex system of filament bundles which appeared morphologically and spatially heterogeneous. Most obvious were long dense bundles of cables traversing along the ventral surface of developing myoblasts, presumably the 'stress fibers' seen in light microscopy. Other bundle types occurred which were composed of loose aggregates of filaments coursing through the remnant cell body. A prominent accumulation of filaments was also seen at the lateral edges of these myoblasts. These lateral edge cables were thicker and denser than any other type of filament bundle observed in the myoblasts. Reaction of unextracted myoblasts directly to human antiplatelet myosin conjugated to rhodamine demonstrated that the most intense reaction also occurred along the lateral edges of both human and chick myoblasts. During development of chick myoblasts the filament bundles became oriented parallel to the cell axis giving the cell a fusiform morphology. It is possible that the various filament bundle structures and their differing structural and spatial dispositions could be related to functional differences among the diverse population of intracellular bundles of filaments.

Entities:  

Mesh:

Substances:

Year:  1980        PMID: 7193921     DOI: 10.1016/0040-8166(80)90015-4

Source DB:  PubMed          Journal:  Tissue Cell        ISSN: 0040-8166            Impact factor:   2.466


  3 in total

Review 1.  Dynamic regulation of sarcomeric actin filaments in striated muscle.

Authors:  Shoichiro Ono
Journal:  Cytoskeleton (Hoboken)       Date:  2010-11

2.  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

3.  Messenger RNA in the cytoskeletal framework: analysis by in situ hybridization.

Authors:  W R Jeffery
Journal:  J Cell Biol       Date:  1982-10       Impact factor: 10.539

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.