Interaction of cortactin and Arp2/3 complex is required for sphingosine-1-phosphate-induced endothelial cell remodeling

Yansong Li, Takehito Uruno, Christian Haudenschild, Steven M. Dudek, Joe G.N. Garcia, Xi Zhan

研究成果: ジャーナルへの寄稿学術誌査読

29 被引用数 (Scopus)

抄録

Sphingosine-1-phosphate (S1P) induces capillary formation of endothelial cells on Matrigel in accompany with actin assembly and accumulation of cortactin and Arp2/3 complex at the cell-leading edge. Suppression of cortactin expression with a cortactin antisense oligo significantly impaired S1P-induced capillary formation, migration of endothelial cells, and actin assembly at the cell periphery. Overexpression of wild-type cortactin tagged by green fluorescent protein (GFP) increased the S1P-induced tube formation and cell motility, whereas the cells overexpressing the mutant formed poorly capillary network and became less motile in response to S1P. Analysis of distribution in Triton X-100 insoluble fractions demonstrated that the cortactin mutant inhibited the association of wild-type cortactin and Arp2/3 complex with the actin-enriched complex. Furthermore, actin polymerization at and distribution of Arp2/3 complex as well as endogenous cortactin into the cell-leading edge mediated by S1P was disturbed. These data suggest that the interaction between cortactin and Arp2/3 complex plays an important role in S1P-mediated remodeling of endothelial cells.

本文言語英語
ページ(範囲)107-121
ページ数15
ジャーナルExperimental Cell Research
298
1
DOI
出版ステータス出版済み - 8月 1 2004
外部発表はい

!!!All Science Journal Classification (ASJC) codes

  • 細胞生物学

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