Concise review: Bone morphogenetic protein pleiotropism in neural stem cells and their derivatives - Alternative pathways, convergent signals

被引:91
作者
Chen, Hui-Ling [1 ]
Panchision, David M. [1 ]
机构
[1] Childrens Natl Med Ctr, Ctr Res Neurosci, Washington, DC 20010 USA
关键词
apoptosis; TGF-beta receptor; proliferation; pleiotropic effects; neural stem cell; neural differentiation; growth factor bone morphogenetic protein; bone morphogenetic protein receptor; Smad proteins; Mammalian target of rapamycin p38 mitogen-activated protein kinase; neural crest;
D O I
10.1634/stemcells.2006-0339
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Bone morphogenetic proteins (BMPs) are a class of morphogens that are critical regulators of the central nervous system (CNS), peripheral nervous system, and craniofacial development. Modulation of BMP signaling also appears to be an important component of the postnatal stem cell niche. However, describing a comprehensive model of BMP actions is complicated by their paradoxical effects in precursor cells, which include dorsal specification, promoting proliferation or mitotic arrest, cell survival or death, and neuronal or glial fate. In addition, in postmitotic neurons BMPs can promote dendritic growth, act as axonal chemorepellants, and stabilize synapses. Although many of these responses depend on interactions with other incoming signals, some reflect the recruitment of distinct BMP signal transduction pathways. In this review, we classify the diverse effects of BMPs on neural cells, focus on the known mechanisms that specify distinct responses, and discuss the remaining challenges in identifying the cellular basis of BMP pleiotropism. Addressing these issues may have importance for stem cell mobilization, differentiation, and cell integration/survival in reparative therapies.
引用
收藏
页码:63 / 68
页数:6
相关论文
共 102 条
[21]   The genetic basis of mammalian neurulation [J].
Copp, AJ ;
Greene, NDE ;
Murdoch, JN .
NATURE REVIEWS GENETICS, 2003, 4 (10) :784-793
[22]   The remyelinating potential and in vitro differentiation of MOG-expressing oligodendrocyte precursors isolated from the adult rat CNS [J].
Crang, AJ ;
Gilson, JM ;
Li, WW ;
Blakemore, WF .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2004, 20 (06) :1445-1460
[23]   DISTINCT SPATIAL AND TEMPORAL EXPRESSION PATTERNS OF 2 TYPE-I RECEPTORS FOR BONE MORPHOGENETIC PROTEINS DURING MOUSE EMBRYOGENESIS [J].
DEWULF, N ;
VERSCHUEREN, K ;
LONNOY, O ;
MOREN, A ;
GRIMSBY, S ;
VANDESPIEGLE, K ;
MIYAZONO, K ;
HUYLEBROECK, D ;
TENDIJKE, P .
ENDOCRINOLOGY, 1995, 136 (06) :2652-2663
[24]   BF-1 interferes with transforming growth factor β signaling by associating with Smad partners [J].
Dou, CL ;
Lee, J ;
Liu, B ;
Liu, F ;
Massague, J ;
Xuan, SH ;
Lai, E .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (17) :6201-6211
[25]   Dual role of brain factor-1 in regulating growth and patterning of the cerebral hemispheres [J].
Dou, CL ;
Li, S ;
Lai, ES .
CEREBRAL CORTEX, 1999, 9 (06) :543-550
[26]  
Dudley AT, 1997, DEV DYNAM, V208, P349
[27]   LIM Kinase1 controls synaptic stability downstream of the type IIBMP receptor [J].
Eaton, BA ;
Davis, GW .
NEURON, 2005, 47 (05) :695-708
[28]   Zic1 represses Math1 expression via interactions with the Math1 enhancer and modulation of Math1 autoregulation [J].
Ebert, PJ ;
Timmer, JR ;
Nakada, Y ;
Helms, AW ;
Parab, PB ;
Liu, Y ;
Hunsaker, TL ;
Johnson, JE .
DEVELOPMENT, 2003, 130 (09) :1949-1959
[29]   BMP-7 and excess glutamate:: Opposing effects on dendrite growth from cerebral cortical neurons in vitro [J].
Esquenazi, S ;
Monnerie, H ;
Kaplan, P ;
Le Roux, P .
EXPERIMENTAL NEUROLOGY, 2002, 176 (01) :41-54
[30]   Transforming growth factor-β and bone morphogenetic proteins:: Cooperative players in chick and murine programmed retinal cell death [J].
Franke, AG ;
Gubbe, C ;
Beier, M ;
Duenker, N .
JOURNAL OF COMPARATIVE NEUROLOGY, 2006, 495 (03) :263-278