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SUBSTRATE-ATTACHED GLYCOPROTEINS MEDIATING ADHESION OF NORMAL AND VIRUS-TRANSFORMED MOUSE FIBROBLASTS

When BALB/c 3T3, simian virus 40 (SV40)-transformed 3T3 (SVT2), and revertant variants of the transformed cells are removed by EGTA treatment from the substrate on which they were grown, they leave behind a layer of glycoprotein which has been characterized biochemically (Terry, A. H. and L. A. Culp...

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Autor principal: Culp, Lloyd A.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1974
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2109354/
https://www.ncbi.nlm.nih.gov/pubmed/4473137
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author Culp, Lloyd A.
author_facet Culp, Lloyd A.
author_sort Culp, Lloyd A.
collection PubMed
description When BALB/c 3T3, simian virus 40 (SV40)-transformed 3T3 (SVT2), and revertant variants of the transformed cells are removed by EGTA treatment from the substrate on which they were grown, they leave behind a layer of glycoprotein which has been characterized biochemically (Terry, A. H. and L. A. Culp. 1974. Biochemistry. 13:414.)—substrate-attached material (SAM). The influence of SAM from normal and from transformed cells on cellular attachment to the substrate, morphology, movement, and growth has been examined. All three cell types displayed a 30% higher plating efficiency when grown on 3T3 SAM. The morphology of SVT2 colonies and of individual SVT2 cells was dramatically affected by growth on 3T3 SAM—the cells (a) were more highly spread on the substrate, (b) resisted crawling over neighboring cells, and (c) resisted movement away from the edge of colonies; SVT2 SAM was not effective in causing these changes. A cell-to-substrate attachment assay using thymidine-radiolabeled cells and untreated or SAM-coated cover slips was developed. SVT2 cells attached to 3T3 SAM- or SVT2 SAM-coated cover slips with a faster initial rate and to a higher saturation level than to untreated substrate, whereas 3T3 and revertant cells exhibited no preference; there was no species specificity in these cell-substrate attachment phenomena. Trypsin-released cells attached much more slowly than EGTA-released cells. 3T3 SAM, however, was not effective in lowering the saturation density of mass cultures of virus-transformed cells. These experiments suggest that the substrate-attached glycoproteins of normal cells affect the cellular adhesivity, morphology, movement, and perhaps growth patterns of virus-transformed cells—i.e., causing partial reversion of these properties of transformed cells to those found in contact-inhibited fibroblasts. A model for the involvement of substrate-attached glycoproteins in cell-to-substrate adhesion, and possibly cell-to-cell adhesion, has been proposed.
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spelling pubmed-21093542008-05-01 SUBSTRATE-ATTACHED GLYCOPROTEINS MEDIATING ADHESION OF NORMAL AND VIRUS-TRANSFORMED MOUSE FIBROBLASTS Culp, Lloyd A. J Cell Biol Article When BALB/c 3T3, simian virus 40 (SV40)-transformed 3T3 (SVT2), and revertant variants of the transformed cells are removed by EGTA treatment from the substrate on which they were grown, they leave behind a layer of glycoprotein which has been characterized biochemically (Terry, A. H. and L. A. Culp. 1974. Biochemistry. 13:414.)—substrate-attached material (SAM). The influence of SAM from normal and from transformed cells on cellular attachment to the substrate, morphology, movement, and growth has been examined. All three cell types displayed a 30% higher plating efficiency when grown on 3T3 SAM. The morphology of SVT2 colonies and of individual SVT2 cells was dramatically affected by growth on 3T3 SAM—the cells (a) were more highly spread on the substrate, (b) resisted crawling over neighboring cells, and (c) resisted movement away from the edge of colonies; SVT2 SAM was not effective in causing these changes. A cell-to-substrate attachment assay using thymidine-radiolabeled cells and untreated or SAM-coated cover slips was developed. SVT2 cells attached to 3T3 SAM- or SVT2 SAM-coated cover slips with a faster initial rate and to a higher saturation level than to untreated substrate, whereas 3T3 and revertant cells exhibited no preference; there was no species specificity in these cell-substrate attachment phenomena. Trypsin-released cells attached much more slowly than EGTA-released cells. 3T3 SAM, however, was not effective in lowering the saturation density of mass cultures of virus-transformed cells. These experiments suggest that the substrate-attached glycoproteins of normal cells affect the cellular adhesivity, morphology, movement, and perhaps growth patterns of virus-transformed cells—i.e., causing partial reversion of these properties of transformed cells to those found in contact-inhibited fibroblasts. A model for the involvement of substrate-attached glycoproteins in cell-to-substrate adhesion, and possibly cell-to-cell adhesion, has been proposed. The Rockefeller University Press 1974-10-01 /pmc/articles/PMC2109354/ /pubmed/4473137 Text en Copyright © 1974 by The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Culp, Lloyd A.
SUBSTRATE-ATTACHED GLYCOPROTEINS MEDIATING ADHESION OF NORMAL AND VIRUS-TRANSFORMED MOUSE FIBROBLASTS
title SUBSTRATE-ATTACHED GLYCOPROTEINS MEDIATING ADHESION OF NORMAL AND VIRUS-TRANSFORMED MOUSE FIBROBLASTS
title_full SUBSTRATE-ATTACHED GLYCOPROTEINS MEDIATING ADHESION OF NORMAL AND VIRUS-TRANSFORMED MOUSE FIBROBLASTS
title_fullStr SUBSTRATE-ATTACHED GLYCOPROTEINS MEDIATING ADHESION OF NORMAL AND VIRUS-TRANSFORMED MOUSE FIBROBLASTS
title_full_unstemmed SUBSTRATE-ATTACHED GLYCOPROTEINS MEDIATING ADHESION OF NORMAL AND VIRUS-TRANSFORMED MOUSE FIBROBLASTS
title_short SUBSTRATE-ATTACHED GLYCOPROTEINS MEDIATING ADHESION OF NORMAL AND VIRUS-TRANSFORMED MOUSE FIBROBLASTS
title_sort substrate-attached glycoproteins mediating adhesion of normal and virus-transformed mouse fibroblasts
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2109354/
https://www.ncbi.nlm.nih.gov/pubmed/4473137
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