Literature DB >> 6268302

Reversible changes in nuclear and cell surface topography in cells exposed to collagenase and EDTA.

S Moskalewski, J Thyberg.   

Abstract

Rabbit auricular chondrocytes, SIRC cells, human fibroblasts, and HeLa cells were cultivated in vitro and the fine structural effects of various detachment procedures studied. Treatment with collagenase, trypsin, and trypsin-EDTA caused scalloping of the nuclear envelope, accumulation of phagolysosomes, and an increase in the number of cell surface extensions. Collagenase-EDTA evoked a marked deformation of the nuclei with formation of numerous deep indentations and a redistribution of heterochromatin. Similarly, the cell surface became extensively folded and the vacuolation of the cytoplasm was further increased. These changes were reversible and within 24 h the cells had regained a normal structure. In all cases, chondrocytes and SIRC cells were most prominently affected, whereas fibroblasts and HeLa cells were only slightly changed. Treatment of chondrocytes with colchicine or cytochalasin B did not produce any effects of the type mentioned above. Neither did treatment with the drugs before and during detachment with collagenase-EDTA prevent the structural modification of the cells. It therefore seems unlikely that microtubules and microfilaments are essential for this process. The structural changes occurring during detachment of cells could represent an adoptive mechanism for disposal of excessive membrane in connection with transition from a flattened to a rounded shape.

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Year:  1981        PMID: 6268302     DOI: 10.1007/bf00209965

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


  23 in total

1.  Microvilli and blebs as sources of reserve surface membrane during cell spreading.

Authors:  C A Erickson; J P Trinkaus
Journal:  Exp Cell Res       Date:  1976-05       Impact factor: 3.905

2.  Influence of colchicine and vinblastine on the golgi complex and matrix deposition in chondrocyte aggregates. An ultrastructural study.

Authors:  S Moskalewski; J Thyberg; S Lohmander; U Friberg
Journal:  Exp Cell Res       Date:  1975-10-15       Impact factor: 3.905

3.  The role of microvilli in the agglutination of cells by concanavalin A.

Authors:  T E Ukena; M J Karnovsky
Journal:  Exp Cell Res       Date:  1977-05       Impact factor: 3.905

4.  Adhesion of culture cells to their substratum.

Authors:  J P Revel; P Hoch; D Ho
Journal:  Exp Cell Res       Date:  1974-03-15       Impact factor: 3.905

5.  A low-viscosity epoxy resin embedding medium for electron microscopy.

Authors:  A R Spurr
Journal:  J Ultrastruct Res       Date:  1969-01

6.  Buffer combinations for mammalian cell culture.

Authors:  H Eagle
Journal:  Science       Date:  1971-10-29       Impact factor: 47.728

7.  Trypsin-induced coordinate alterations in cell shape, cytoskeleton, and intrinsic membrane structure of contact-inhibited cells.

Authors:  L T Furcht; G Wendelschafer-Crabb
Journal:  Exp Cell Res       Date:  1978-06       Impact factor: 3.905

8.  Effects of hyaluronidase, trypsin, and EDTA on surface composition and topography during detachment of cells in culture.

Authors:  K G Vogel
Journal:  Exp Cell Res       Date:  1978-05       Impact factor: 3.905

9.  Surface morphology and agglutinability with concanavalin A in normal and transformed murine fibroblasts.

Authors:  J G Collard; J H Temmink
Journal:  J Cell Biol       Date:  1976-01       Impact factor: 10.539

10.  Reversibly contractile nuclear matrix. Its isolation, structure, and composition.

Authors:  F Wunderlich; G Herlan
Journal:  J Cell Biol       Date:  1977-05       Impact factor: 10.539

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  1 in total

1.  Influence of proteolytic enzymes and calcium-binding agents on nuclear and cell surface topography.

Authors:  J Thyberg; S Moskalewski
Journal:  Cell Tissue Res       Date:  1984       Impact factor: 5.249

  1 in total

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