TY - JOUR
T1 - Roles of STEF/Tiam1, guanine nucleotide exchange factors for Rac1, in regulation of growth cone morphology
AU - Matsuo, Naoki
AU - Terao, Mami
AU - Nabeshima, Yo Ichi
AU - Hoshino, Mikio
N1 - Funding Information:
We are grateful to M. Sone, M. Yoshizawa, T. Kawauchi, C. Hama, and R.T. Yu for helpful comments. We also thank A. Hall and K. Kaibuchi for C3 transferase plasmid. This work was supported in part by Grants-in-Aid for Scientific Research on Priority Areas (C) Advanced Brain Science Project, (C) Genome Science, and (A) Research for Comprehensive Promotion of Study of Brain (to M.H.) from the Ministry of Education, Culture, Sports, and Science and Technology, Japan. N.M. was supported by Research Fellowships of the Japan Society for the Promotion of Science (JSPS) for Young Scientists.
PY - 2003/9/1
Y1 - 2003/9/1
N2 - Rho family GTPases are suggested to be pivotal for growth cone behavior, but regulation of their activities in response to environmental cues remains elusive. Here, we describe roles of STEF and Tiam1, guanine nucleotide exchange factors for Rac1, in neurite growth and growth cone remodeling. We reveal that, in primary hippocampal neurons, STEF/Tiam1 are localized within growth cones and essential for formation of growth cone lamellipodia, eventually contributing to neurite growth. Furthermore, experiments using a dominant-negative form demonstrate that STEF/Tiam1 mediate extracellular laminin signals to activate Rac1, promoting neurite growth in N1E-115 neuroblastoma cells. STEF/Tiam1 are revealed to mediate Cdc42 signal to activate Rac1 during lamellipodial formation. We also show that RhoA inhibits the STEF/Tiam1-Rac1 pathway. These data are used to propose a model that extracellular and intracellular information is integrated by STEF/Tiam1 to modulate the balance of Rho GTPase activities in the growth cone and, consequently, to control growth cone behavior.
AB - Rho family GTPases are suggested to be pivotal for growth cone behavior, but regulation of their activities in response to environmental cues remains elusive. Here, we describe roles of STEF and Tiam1, guanine nucleotide exchange factors for Rac1, in neurite growth and growth cone remodeling. We reveal that, in primary hippocampal neurons, STEF/Tiam1 are localized within growth cones and essential for formation of growth cone lamellipodia, eventually contributing to neurite growth. Furthermore, experiments using a dominant-negative form demonstrate that STEF/Tiam1 mediate extracellular laminin signals to activate Rac1, promoting neurite growth in N1E-115 neuroblastoma cells. STEF/Tiam1 are revealed to mediate Cdc42 signal to activate Rac1 during lamellipodial formation. We also show that RhoA inhibits the STEF/Tiam1-Rac1 pathway. These data are used to propose a model that extracellular and intracellular information is integrated by STEF/Tiam1 to modulate the balance of Rho GTPase activities in the growth cone and, consequently, to control growth cone behavior.
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U2 - 10.1016/S1044-7431(03)00122-2
DO - 10.1016/S1044-7431(03)00122-2
M3 - Article
C2 - 14550769
AN - SCOPUS:0042997222
SN - 1044-7431
VL - 24
SP - 69
EP - 81
JO - Molecular and Cellular Neuroscience
JF - Molecular and Cellular Neuroscience
IS - 1
ER -