Involvement of small GTPases Rho and Rac in the invasion of rat ascites hepatoma cells

被引:31
作者
Imamura, F
Mukai, M
Ayaki, M
Takemura, K
Horai, T
Shinkai, K
Nakamura, H
Akedo, H
机构
[1] Osaka Med Ctr Canc & Cardiovasc Dis, Dept Pulm Oncol, Higashinari Ku, Osaka 537, Japan
[2] Osaka Med Ctr Canc & Cardiovasc Dis, Dept Tumor Biochem, Higashinari Ku, Osaka 537, Japan
[3] Osaka Med Ctr Canc & Cardiovasc Dis, Dept Pathol, Higashinari Ku, Osaka 537, Japan
关键词
cell surface blebbing; invasion; pseudopodia; Rac; Rho;
D O I
10.1023/A:1006598531238
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Lysophosphatidic acid (LPA) triggers the invasion of a mesothelial cell monolayer by rat ascites hepatoma (MM1) cells. LPA also induces rapid morphological changes of MM1 cells, cell surface blebbing and pseudopodia formation. Pseudopodia formation is tightly correlated with cellular invasiveness. Clostridium Botulinum C3 exoenzyme and genistein abrogated the formation of blebs and pseudopodia together with the inhibition of invasion, indicating that GTPase Rho and certain tyrosine kinases are involved in both processes. MM1 cells expressing constitutively active Rho exhibited the invasion and the formation of blebs and pseudopodia in the absence of LPA. In contrast, MM1 cells expressing constitutively active Rac were not invasive in the absence of LPA, but were invasive in the presence of LPA. Their morphological response to LPA was almost the same as that of parental MM1 cells. Expression of dominant negative Rac suppressed the invasiveness to approximately 3% of that of parental MM1 cells, together with the inhibition of pseudopodia formation. Thus, Rho and Rac are cooperatively involved in both the invasion and the related morphological changes of MM1 cells. Rho activation is sufficient both for the induction of invasion and the morphological changes leading to the invasion, whereas Rac activation is necessary but not sufficient by itself. We propose that Rho activation is not mediated by Rac but the cooperation of both GTPases is essential to trigger the invasive behavior of MM1 cells.
引用
收藏
页码:141 / 148
页数:8
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