Neurotrophin 3 activation of TrkC induces Schwann cell migration through the c-Jun N-terminal kinase pathway

被引:121
作者
Yamauchi, J
Chan, JR
Shooter, EM
机构
[1] Stanford Univ, Sch Med, Dept Neurobiol, Stanford, CA 94305 USA
[2] Nara Inst Sci & Technol, Dept Cell Biol, Nara 6300101, Japan
关键词
D O I
10.1073/pnas.2336152100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
During development and nerve injury, complex interactions between glial cells and neurons are essential for establishing proper nerve function. Neurotrophins play multiple roles in the developing nervous system, including cell survival, growth, and differentiation. Here we show that migration of Schwann cells, isolated from sciatic nerves, is significantly enhanced by neurotrophin 3, but not by nerve growth factor or brain-derived neurotrophic factor. The neurotrophin-3-induced cell migration was also observed in Schwann cells isolated from sciatic nerves of p(75NTR-/-) mice, indicating that neurotrophin 3 enhances cell migration through TrkC. This effect was blocked by K252a, an inhibitor of the Trk receptor family. Additionally, the neurotrophin-3-induced cell migration depended on Rho GTPases (Rac1 and Cdc42) and c-Jun N-terminal kinase. We obtained the same results with Cos-7 cells expressing TrkC. Taken together, these results suggest that neurotrophin 3 activation of TrkC induces Schwann cell migration through the c-Jun N-terminal kinase signaling pathway.
引用
收藏
页码:14421 / 14426
页数:6
相关论文
共 36 条
[1]   Structural basis for relief of autoinhibition of the Dbl homology domain of proto-oncogene Vav by tyrosine phosphorylation [J].
Aghazadeh, B ;
Lowry, WE ;
Huang, XY ;
Rosen, MK .
CELL, 2000, 102 (05) :625-633
[2]   Ras and Rho GTPases: A family reunion [J].
Bar-Sagi, D ;
Hall, A .
CELL, 2000, 103 (02) :227-238
[3]   SP600125, an anthrapyrazolone inhibitor of Jun N-terminal kinase [J].
Bennett, BL ;
Sasaki, DT ;
Murray, BW ;
O'Leary, EC ;
Sakata, ST ;
Xu, WM ;
Leisten, JC ;
Motiwala, A ;
Pierce, S ;
Satoh, Y ;
Bhagwat, SS ;
Manning, AM ;
Anderson, DW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (24) :13681-13686
[4]   FIBRONECTIN AND POLYLYSINE REQUIREMENT FOR PROLIFERATION OF NEURO-BLASTOMA CELLS IN DEFINED MEDIUM [J].
BOTTENSTEIN, JE ;
SATO, GH .
EXPERIMENTAL CELL RESEARCH, 1980, 129 (02) :361-366
[5]   NEURON SCHWANN-CELL INTERACTION IN BASAL LAMINA FORMATION [J].
BUNGE, MB ;
WILLIAMS, AK ;
WOOD, PM .
DEVELOPMENTAL BIOLOGY, 1982, 92 (02) :449-460
[6]  
Bunge R P, 1993, Curr Opin Neurobiol, V3, P805, DOI 10.1016/0959-4388(93)90157-T
[7]   A CONSERVED BINDING MOTIF DEFINES NUMEROUS CANDIDATE TARGET PROTEINS FOR BOTH CDC42 AND RAC GTPASES [J].
BURBELO, PD ;
DRECHSEL, D ;
HALL, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (49) :29071-29074
[8]   Glucocorticoids and progestins signal the initiation and enhance the rate of myelin formation [J].
Chan, JR ;
Phillips, LJ ;
Glaser, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (18) :10459-10464
[9]   EXPRESSION OF THE NEU PROTOONCOGENE BY SCHWANN-CELLS DURING PERIPHERAL-NERVE DEVELOPMENT AND WALLERIAN DEGENERATION [J].
COHEN, JA ;
YACHNIS, AT ;
ARAI, M ;
DAVIS, JG ;
SCHERER, SS .
JOURNAL OF NEUROSCIENCE RESEARCH, 1992, 31 (04) :622-634
[10]   The neurotrophin receptor p75NTR as a positive modulator of myelination [J].
Cosgaya, JM ;
Chan, JR ;
Shooter, EM .
SCIENCE, 2002, 298 (5596) :1245-1248