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JSAP1 is required for the cell adhesion and spreading of mouse embryonic fibroblasts
Authors:Chae Hee-Jung  Ha Hye-Yeong  Im Joo-Young  Song Ji-Young  Park Sungmi  Han Pyung-Lim
Affiliation:Division of Nano Sciences and Ewha Institute of Neuroscience, Ewha Womans University, Seoul 120-750, Republic of Korea.
Abstract:The roles of JSAP1 and JIP1 in cell adhesion and spreading were examined using mouse embryonic fibroblasts (MEFs) deficient in JIP1 (JIP1-KO), JSAP1 (JSAP1-KO), and in both JIP1 and JSAP1 (double-KO), and by using their wild type. After being plated on fibronectin-coated culture plates, wild type MEFs rapidly adhered and differentiated to typical longitudinal fibroblasts in 4 h. JSAP1-KO MEFs showed a similar sequence of adhesion and cell spreading, but their adhesion was weak, and cell spreading sequence proceeded in a delayed manner compared with the wild type. In spreading JSAP1-KO MEFs, adhesion-triggered actin cytoskeleton reorganization and FAK activation proceeded at a slower pace than in wild type MEFs. The cellular properties of double-KO MEFs and JIP1-KO MEFs were similar to those of JSAP1-KO MEFs and wild type MEFs, respectively. These results suggest that JSAP1 plays a role in adhesion and cell spreading by regulating the rapid reorganization of the actin cytoskeleton.
Keywords:Scaffold protein   FAK   Cell adhesion   Actin filaments
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