Grit, a GTPase-activating protein for the Rho family, regulates neurite extension through association with the TrkA receptor and N-Shc and CrkL/Crk adapter molecules

被引:84
作者
Nakamura, T
Komiya, M
Sone, K
Hirose, E
Gotoh, N
Morii, H
Ohta, Y
Mori, N [1 ]
机构
[1] Natl Inst Longev Sci, Dept Mol Genet, Aichi 4748522, Japan
[2] JST, CREST, Program Protecting Brain, Aichi 4748522, Japan
[3] Sumitomo Elect Ind Ltd, Biomed R&D Dept, Yokohama, Kanagawa 2448588, Japan
[4] NYU, Sch Med, Dept Pharmacol, New York, NY 10016 USA
[5] NYU, Sch Med, Skirball Inst, New York, NY 10016 USA
[6] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Med,Hematol Div, Boston, MA 02115 USA
关键词
D O I
10.1128/MCB.22.24.8721-8734.2002
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
Neurotrophins are key regulators of the fate and shape of neuronal cells and act as guidance cues for growth cones by remodeling the actin cytoskeleton. Actin dynamics is controlled by Rho GTPases. We identified a novel Rho GTPase-activating protein (Grit) for Rho/Rac/Cdc42 small GTPases. Grit was abundant in neuronal cells and directly interacted with TrkA, a high-affinity receptor for nerve growth factor (NGF). Another pool of Grit was recruited to the activated receptor tyrosine kinase through its binding to N-Shc and CrkL/Crk, adapter molecules downstream of activated receptor tyrosine kinases. Overexpression of the TrkA-binding region of Grit inhibited NGF-induced neurite elongation. Further, we found some tendency for neurite promotion in full-length Grit-overexpres sing PC12 cells upon NGF stimulation. These results suggest that Grit, a novel TrkA-interacting protein, regulates neurite outgrowth by modulating the Rho family of small GTPases.
引用
收藏
页码:8721 / 8734
页数:14
相关论文
共 62 条
[1]   Overexpression of a neural-specific Rho family GTPase, cRac1B, selectively induces enhanced neuritogenesis and neurite branching in primary neurons [J].
Albertinazzi, C ;
Gilardelli, D ;
Paris, S ;
Longhi, R ;
de Curtis, I .
JOURNAL OF CELL BIOLOGY, 1998, 142 (03) :815-825
[2]   Integrin engagement suppresses RhoA activity via a c-Src-dependent mechanism [J].
Arthur, WT ;
Petch, LA ;
Burridge, K .
CURRENT BIOLOGY, 2000, 10 (12) :719-722
[3]   Essential role of neural Wiskott-Aldrich syndrome protein in neurite extension in PC12 cells and rat hippocampal primary culture cells [J].
Banzai, Y ;
Miki, H ;
Yamaguchi, H ;
Takenawa, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (16) :11987-11992
[4]   Biochemical and functional interactions between the neurotrophin receptors trk and p75NTR [J].
Bibel, M ;
Hoppe, E ;
Barde, YA .
EMBO JOURNAL, 1999, 18 (03) :616-622
[5]   Neurotrophins: key regulators of cell fate and cell shape in the vertebrate nervous system [J].
Bibel, M ;
Barde, YA .
GENES & DEVELOPMENT, 2000, 14 (23) :2919-2937
[6]   Rho GTPases and their effector proteins [J].
Bishop, AL ;
Hall, A .
BIOCHEMICAL JOURNAL, 2000, 348 (02) :241-255
[7]   Not all Shc's roads lead to Ras [J].
Bonfini, L ;
Migliaccio, E ;
Pelicci, G ;
Lanfrancone, L ;
Pelicci, P .
TRENDS IN BIOCHEMICAL SCIENCES, 1996, 21 (07) :257-261
[8]  
Brouns MR, 2000, DEVELOPMENT, V127, P4891
[9]   p190 RhoGAP is the principal Src substrate in brain and regulates axon outgrowth, guidance and fasciculation [J].
Brouns, MR ;
Matheson, SF ;
Settleman, J .
NATURE CELL BIOLOGY, 2001, 3 (04) :361-367
[10]   Translocation of the Rac1 guanine nucleotide exchange factor Tiam1 induced by platelet-derived growth factor and lysophosphatidic acid [J].
Buchanan, FG ;
Elliot, CM ;
Gibbs, M ;
Exton, JH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (13) :9742-9748