Literature DB >> 14126869

THE MECHANISM OF ADHESION OF CELLS TO GLASS. A STUDY BY INTERFERENCE REFLECTION MICROSCOPY.

A S CURTIS.   

Abstract

An optical technique for measuring the thickness of thin films has been adapted and evaluated for studying the structure of the adhesion of cells to glass in tissue culture. This technique, which is termed interference reflection microscopy, has been used to study embryonic chick heart fibroblasts. These findings have been observed: in normal culture medium the closest approach of the cell surface to substrate in its adhesions is ca. 100 A, much of the cell surface lying farther away; chemical treatments which bring the cell surface to near its charge reversal point reduce the closest approach of adhesions to <50 A, probably to <30 A; chemical treatments which increase surface charge increase the nearest approach of cell and substrate in adhesions from ca. 100 A; high osmotic concentration of a non-polar substance, i.e. sucrose, does not affect the distance between cell and substrate in the adhesions. In addition, optical evidence indicates that there is no extracellular material between cell and glass in the adhesions. When cells de-adhere from glass, they appear not to leave fragments behind. The adhesive sites in these fibroblasts appear to be confined to the edge of the side of the cell facing the substrate and to the pseudopods. The significance of this is discussed in relation to the phenomenon of contact inhibition. Evidence is presented that the mechanism of cell adhesion does not involve calcium atoms binding cells to substrate by combining with carboxyl groups on cell surface, substrate, and with a cement substance. Osmium tetroxide fixation results in a final separation of 100 to 200 A between cell and substrate: there are reasons for thinking that this fairly close approach to the condition in life is produced as an artefact. The results can be accounted for only in terms of the action of electrostatic repulsive forces and an attractive force, probably the van der Waals-London forces. Biological arguments suggest that these results are equally applicable for cell-to-cell adhesions.

Entities:  

Keywords:  CHICK EMBRYO; CYTOLOGY; EXPERIMENTAL LAB STUDY; GLASS; MICROSCOPY; MICROSCOPY, INTERFERENCE; MYOCARDIUM; TISSUE CULTURE

Mesh:

Year:  1964        PMID: 14126869      PMCID: PMC2106393          DOI: 10.1083/jcb.20.2.199

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  10 in total

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  132 in total

Review 1.  Evanescent-wave microscopy: a new tool to gain insight into the control of transmitter release.

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Authors:  Elodie Cretel; Anne Pierres; Anne-Marie Benoliel; Pierre Bongrand
Journal:  Cell Mol Bioeng       Date:  2008-03       Impact factor: 2.321

Review 8.  Integrative systems and synthetic biology of cell-matrix adhesion sites.

Authors:  Eli Zamir
Journal:  Cell Adh Migr       Date:  2016-02-06       Impact factor: 3.405

9.  Redistribution of microfilament-associated proteins during the formation of focal contacts and adhesions in chick fibroblasts.

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10.  Interference reflection microscopy.

Authors:  Valarie A Barr; Stephen C Bunnell
Journal:  Curr Protoc Cell Biol       Date:  2009-12
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