JS']JSAP1 is required for the cell adhesion and spreading of mouse embryonic fibroblasts

被引:4
作者
Chae, Hee-Jung
Ha, Hye-Yeong
Im, Joo-Young
Song, Ii-Young
Park, Sungmi
Han, Pyung-Lim [1 ]
机构
[1] Ewha Womans Univ, Div Nanosci, Seoul 120750, South Korea
[2] Ewha Womans Univ, Ewha Inst Neurosci, Seoul 120750, South Korea
基金
新加坡国家研究基金会;
关键词
scaffold protein; FAK; cell adhesion; actin filaments;
D O I
10.1016/j.bbrc.2006.05.005
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
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 oil fibronectin-coated culture plates, wild type MEFs rapidly adhered and differentiated to typical longitudinal fibroblasts in 4h. 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. (c) 2006 Elsevier Inc, All rights reserved.
引用
收藏
页码:809 / 816
页数:8
相关论文
共 30 条
[1]   Matrix survival signaling:: From fibronectin via focal adhesion kinase to c-Jun NH2-terminal kinase [J].
Almeida, EAC ;
Ilic, D ;
Han, Q ;
Hauck, CR ;
Jin, F ;
Kawakatsu, H ;
Schlaepfer, DD ;
Damsky, CH .
JOURNAL OF CELL BIOLOGY, 2000, 149 (03) :741-754
[2]  
BURRIDGE K, 1988, ANNU REV CELL BIOL, V4, P487, DOI 10.1146/annurev.cb.04.110188.002415
[3]   Active ERK/MAP kinase is targeted to newly forming cell-matrix adhesions by integrin engagement and v-Src [J].
Fincham, VJ ;
James, M ;
Frame, MC ;
Winder, SJ .
EMBO JOURNAL, 2000, 19 (12) :2911-2923
[4]   A direct interaction between JNK1 and CrkII is critical for Rac1-induced JNK activation [J].
Girardin, SE ;
Yaniv, M .
EMBO JOURNAL, 2001, 20 (13) :3437-3446
[5]   The axon guidance defect of the telencephalic commissures of the JS']JSAP1-deficient brain was partially rescued by the transgenic expression of JIP1 [J].
Ha, HY ;
Cho, IH ;
Lee, KW ;
Lee, KW ;
Song, JY ;
Kim, KS ;
Yu, YM ;
Lee, JK ;
Song, JS ;
Yang, SD ;
Shin, HS ;
Han, PL .
DEVELOPMENTAL BIOLOGY, 2005, 277 (01) :184-199
[6]   Divergent signaling pathways link focal adhesion kinase to mitogen-activated protein kinase cascades -: Evidence for a role of paxillin in c-Jun NH2-terminal kinase activation [J].
Igishi, T ;
Fukuhara, S ;
Patel, V ;
Katz, BZ ;
Yamada, KR ;
Gutkind, JS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (43) :30738-30746
[7]  
Ilic Dusko, 1995, Nature (London), V377, P539, DOI 10.1038/377539a0
[8]   Repression of phospho-JNK and infarct volume in ischemic brain of JIP1-deficient mice [J].
Im, JY ;
Lee, KW ;
Kim, MH ;
Lee, SH ;
Ha, HY ;
Cho, IH ;
Kim, D ;
Yu, MS ;
Kim, JB ;
Lee, JK ;
Kim, YJ ;
Youn, BW ;
Yang, SD ;
Shin, HS ;
Han, PL .
JOURNAL OF NEUROSCIENCE RESEARCH, 2003, 74 (02) :326-332
[9]  
Ito M, 1999, MOL CELL BIOL, V19, P7539
[10]   Morphogenesis of the telencephalic commissure requires scaffold protein JNK-interacting protein 3 (JIP3) [J].
Kelkar, N ;
Delmotte, MH ;
Weston, CR ;
Barrett, T ;
Sheppard, BJ ;
Flavell, RA ;
Davis, RJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (17) :9843-9848