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Substrate‐attached serum and cell proteins in adhesion of mouse fibroblasts
Author(s) -
Culp Lloyd A.,
Buniel Josefina F.
Publication year - 1976
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.1040880111
Subject(s) - 3t3 cells , substrate (aquarium) , concanavalin a , trypsin , cell adhesion , cell , cell culture , microbiology and biotechnology , biophysics , chemistry , biology , biochemistry , enzyme , in vitro , transfection , ecology , genetics
Abstract The effects of serum and coatings of substrate‐attached material (SAM, which remains tightly adherent to the substrate after EGTA‐mediated removal of cells) on the kinetics of attachment of DNA‐radiolabeled BALB/c 3T3, SV40‐transformed 3T3, and concanavalin A‐selected revertant cells to glass coverslips were studied. The presence of serum in the medium of attaching cells had a marked effect on (1) the initial time lag before stable attachment of cells, (2) the maximum level of attached cells, (3) the stability of attachment, and (4) pseudopodial spread of the cell over the substrate. These serum effects could be mimicked by measuring attachment in medium without serum and with use of serum‐preadsorbed or 3T3 SAM‐coated coverslips. Enzymatic treatment of serum‐preadsorbed substrates indicated that the factor(s) in serum which affects attachment is very trypsin‐sensitive. Serum preadsorption of substrates stimulated attachment of SVT2 cells in medium with serum in a manner very similar to the effects of 3T3 SAM coatings, while attachment of 3T3 or revertant cells was unaffected. Slab gel electrophoretic analysis (PAGE‐SDS gels) identified eight major serum proteins by Coomassie blue staining (a) which bind to the substrate in the absence of cells and (b) which persist on the substrate after growth to confluence of 3T3 or SVT2 cells; this suggests that major breakdown of serum‐adsorbed components does not occur during growth of normal or transformed cells. Seven radioactive SAM proteins were detected by autoradiography in 3T3 or SVT2 SAM electropherograms — two of which are high molecular weight components which correspond to the glucosamine‐radiolabeled hyaluronate proteoglycans observed previously; the remaining five are newly‐identified proteins in SAM (one of these proteins appears to be actin). 3T3 and SVT2 cells have unique proportions of these seven components. The data are consistent with the idea that normal or virus‐transformed cells do not attach directly to the culture substrate, but to specific classes of substrate‐adsorbed serum proteins via deposition of specific classes of cell surface proteins and polysaccharides.