Effect of microtubule disruption on cell adhesion and spreading

被引:50
作者
Kadi, A [1 ]
Pichard, V [1 ]
Lehmann, M [1 ]
Briand, C [1 ]
Braguer, D [1 ]
Marvaldi, J [1 ]
Rognoni, JB [1 ]
Luis, J [1 ]
机构
[1] Fac Pharm Marseille, Biochim Cellulaire Lab, CNRS, UPRES A 6032, F-13385 Marseille 5, France
关键词
integrin; cytoskeleton; nocodazole; navelbine; paclitaxel; adhesion; spreading; collagen;
D O I
10.1006/bbrc.1998.8536
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Microtubules have been involved in a variety of cellular processes. In this study, we examined the role of the microtubular system in the adhesion and spreading of the adenocarcinoma cell line HT29-D4. Disruption of microtubules by nocodazole or navelbine resulted in an increase in cell adhesion to purified ECM proteins. This enhanced cell adhesion is mediated by integrins, but is not attributable to quantitative changes in the number of integrin receptors at the cell surface, as determined by how cytometric analysis. In contrast to attachment, spreading of HT29-D4 cells was reduced by nocodazole treatment in a dose-dependent manner. Thus, microtubule depolymerization appears to increase initial attachment of cells to extracellular matrix, while impeding subsequent cell spreading. (C) 1998 Academic Press.
引用
收藏
页码:690 / 695
页数:6
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