BDNF regulates primary dendrite formation in cortical neurons via the PI3-kinase and MAP kinase signaling pathways

被引:131
作者
Dijkhuizen, PA [1 ]
Ghosh, A [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Neurosci, Baltimore, MD 21205 USA
来源
JOURNAL OF NEUROBIOLOGY | 2005年 / 62卷 / 02期
关键词
neurotrophin; dendrite; cortex; pyramidal neuron; PI3-kinase; MAP kinase;
D O I
10.1002/neu.20100
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neurotrophins are known to regulate dendritic development, but the mechanisms that mediate neurotrophin-dependent dendrite formation are largely unknown. Here we show that brain-derived neurotrophic factor (BDNF) induces the formation of primary dendrites in cortical neurons by a protein synthesis-independent mechanism. BDNF leads to the rapid activation of PI3-kinase, MAP kinase, and PLC-gamma in cortical neurons, and pharmacological inhibition of PI3-kinase and MAP kinase in dissociated cell cultures and cortical slice cultures suppresses the ability of BDNF to induce dendrite formation. A constitutively active form of PI3-kinase, but not MEK, is sufficient to induce primary dendrite formation in cortical neurons. These observations indicate that BDNF induces primary dendrite formation via activation of the PI3-kinase and MAP kinase pathways and provide insight into the mechanisms that mediate the morphological effects of neurotrophin signaling. (C) 2004 Wiley Periodicals, Inc.
引用
收藏
页码:278 / 288
页数:11
相关论文
共 43 条
[1]   The TrkB-Shc site signals neuronal survival and local axon growth via MEK and PI3-kinase [J].
Atwal, JK ;
Massie, B ;
Miller, FD ;
Kaplan, DR .
NEURON, 2000, 27 (02) :265-277
[2]   Growth of pyramidal, but not non-pyramidal, dendrites in long-term organotypic explants of neonatal rat neocortex chronically exposed to neurotrophin-3 [J].
Baker, RE ;
Dijkhuizen, PA ;
Van Pelt, J ;
Verhaagen, J .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1998, 10 (03) :1037-1044
[3]   Cellular survival: a play in three Akts [J].
Datta, SR ;
Brunet, A ;
Greenberg, ME .
GENES & DEVELOPMENT, 1999, 13 (22) :2905-2927
[4]   Specificity and mechanism of action of some commonly used protein kinase inhibitors [J].
Davies, SP ;
Reddy, H ;
Caivano, M ;
Cohen, P .
BIOCHEMICAL JOURNAL, 2000, 351 (351) :95-105
[5]   MEK inhibitors: The chemistry and biological activity of U0126, its analogs, and cyclization products [J].
Duncia, JV ;
Santella, JB ;
Higley, CA ;
Pitts, WJ ;
Wityak, J ;
Frietze, WE ;
Rankin, FW ;
Sun, JH ;
Earl, RA ;
Tabaka, AC ;
Teleha, CA ;
Blom, KF ;
Favata, MF ;
Manos, EJ ;
Daulerio, AJ ;
Stradley, DA ;
Horiuchi, K ;
Copeland, RA ;
Scherle, PA ;
Trzaskos, JM ;
Magolda, RL ;
Trainor, GL ;
Wexler, RR ;
Hobbs, FW ;
Olson, RE .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1998, 8 (20) :2839-2844
[6]   Phosphoinositide kinases [J].
Fruman, DA ;
Meyers, RE ;
Cantley, LC .
ANNUAL REVIEW OF BIOCHEMISTRY, 1998, 67 :481-507
[7]  
GRAY A, 1999, BIOCHEM J, V15, P929
[8]   Microtubules and signal transduction [J].
Gundersen, GG ;
Cook, TA .
CURRENT OPINION IN CELL BIOLOGY, 1999, 11 (01) :81-94
[9]   Role of substrates and products of PI3-kinase in regulating activation of Rac-related guanosine triphosphatases by Vav [J].
Han, JW ;
Luby-Phelps, K ;
Das, B ;
Shu, XD ;
Xia, Y ;
Mosteller, RD ;
Krishna, UM ;
Falck, JR ;
White, MA ;
Broek, D .
SCIENCE, 1998, 279 (5350) :558-560
[10]  
Horch HW, 1999, NEURON, V23, P353