Coupling cell cycle exit, neuronal differentiation and migration in cortical neurogenesis

被引:90
作者
Nguyen, Laurent
Besson, Arnaud
Roberts, James M.
Guillemot, Francois
机构
[1] Natl Inst Med Res, Div Mol Neurobiol, London NW7 1AA, England
[2] Fred Hutchinson Canc Res Ctr, Howard Hughes Med Inst, Div Basic Sci, Seattle, WA 98104 USA
基金
英国医学研究理事会;
关键词
p27(Kip1); radial migration; RhoA; neuronal differentiation; Ngn2;
D O I
10.4161/cc.5.20.3381
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
The generation of new neurons in the cerebral cortex requires that progenitor cells leave the cell cycle and activate specific programs of differentiation and migration. Genetic studies have identified some of the molecules controlling these cellular events, but how the different aspects of neurogenesis are integrated into a coherent develop mental program remains unclear. One possible mechanism implicates multifunctional proteins that regulate, both cell cycle exit and cell differentiation.(1) A prime example is the cyclin-dependent kinase inhibitor p27(Kip1), which has recently been shown to function beyond cell cycle regulation and promote both neuronal differentiation and migration of newborn cortical neurons, through distinct and separable mechanisms. p27(Kip1) is there fore part of a machinery that couples the multiple events of neurogenesis in the cerebral cortex.
引用
收藏
页码:2314 / 2318
页数:5
相关论文
共 56 条
[1]
p27Kip1-stathmin interaction influences sarcoma cell migration and invasion [J].
Baldassarre, G ;
Belletti, B ;
Nicoloso, MS ;
Schiappacassi, M ;
Vecchione, A ;
Spessotto, P ;
Morrione, A ;
Canzonieri, V ;
Colombatti, A .
CANCER CELL, 2005, 7 (01) :51-63
[2]
Key role of the cyclin-dependent kinase inhibitor p27kip1 for embryonal carcinoma cell survival and differentiation [J].
Baldassarre, G ;
Barone, MV ;
Belletti, B ;
Sandomenico, C ;
Bruni, P ;
Spiezia, S ;
Boccia, A ;
Vento, MT ;
Romano, A ;
Pepe, S ;
Fusco, A ;
Viglietto, G .
ONCOGENE, 1999, 18 (46) :6241-6251
[3]
Proneural genes and the specification of neural cell types [J].
Bertrand, N ;
Castro, DS ;
Guillemot, F .
NATURE REVIEWS NEUROSCIENCE, 2002, 3 (07) :517-530
[4]
p27Kip1 modulates cell migration through the regulation of RhoA activation [J].
Besson, A ;
Gurian-West, M ;
Schmidt, A ;
Hall, A ;
Roberts, JM .
GENES & DEVELOPMENT, 2004, 18 (08) :862-876
[5]
A pathway in quiescent cells that controls p27Kip1 stability, subcellular localization, and tumor suppression [J].
Besson, A ;
Gurian-West, M ;
Chen, XY ;
Kelly-Spratt, KS ;
Kemp, CJ ;
Roberts, JM .
GENES & DEVELOPMENT, 2006, 20 (01) :47-64
[6]
Campagne MV, 1998, J COMP NEUROL, V397, P181
[7]
NEOCORTICAL HISTOGENESIS IN NORMAL AND REELER MICE - A DEVELOPMENTAL-STUDY BASED UPON [H-3] THYMIDINE AUTORADIOGRAPHY [J].
CAVINESS, VS .
DEVELOPMENTAL BRAIN RESEARCH, 1982, 4 (03) :293-302
[8]
Cell output, cell cycle duration and neuronal specification: a model of integrated mechanisms of the neocortical proliferative process [J].
Caviness, VS ;
Goto, T ;
Tarui, T ;
Takahashi, T ;
Bhide, PG ;
Nowakowski, RS .
CEREBRAL CORTEX, 2003, 13 (06) :592-598
[9]
Coordinate control of proliferation and migration by the p27Kip1/cyclin-dependent kinase/retinoblastoma pathway in vascular smooth muscle cells and fibroblasts [J].
Díez-Juan, A ;
Andrés, V .
CIRCULATION RESEARCH, 2003, 92 (04) :402-410
[10]
CDK INHIBITORS - ON THE THRESHOLD OF CHECKPOINTS AND DEVELOPMENT [J].
ELLEDGE, SJ ;
HARPER, JW .
CURRENT OPINION IN CELL BIOLOGY, 1994, 6 (06) :847-852