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
[31]  
Furuta Y, 1997, DEVELOPMENT, V124, P2203
[32]   Bone morphogenetic protein receptor complexes on the surface of live cells:: A new oligomerization mode for serine/threonine kinase receptors [J].
Gilboa, L ;
Nohe, A ;
Geissendörfer, T ;
Sebald, W ;
Henis, YI ;
Knaus, P .
MOLECULAR BIOLOGY OF THE CELL, 2000, 11 (03) :1023-1035
[33]   Neural crest apoptosis and the establishment of craniofacial pattern: An Honorable death [J].
Graham, A ;
Koentges, G ;
Lumsden, A .
MOLECULAR AND CELLULAR NEUROSCIENCE, 1996, 8 (2-3) :76-83
[34]   Brain-derived neurotrophic factor (BDNF) mediates bone morphogenetic protein-2 (BMP-2) effects on cultured striatal neurones [J].
Gratacòs, E ;
Checa, N ;
Pérez-Navarro, E ;
Alberch, J .
JOURNAL OF NEUROCHEMISTRY, 2001, 79 (04) :747-755
[35]   Bone morphogenetic proteins promote astroglial lineage commitment by mammalian subventricular zone progenitor cells [J].
Gross, RE ;
Mehler, MF ;
Mabie, PC ;
Zang, ZY ;
Santschi, L ;
Kessler, JA .
NEURON, 1996, 17 (04) :595-606
[36]  
Gulacsi A, 2003, J NEUROSCI, V23, P9862
[37]   Leukemia inhibitory factor and ciliary neurotrophic factor regulate dendritic growth in cultures of rat sympathetic neurons [J].
Guo, X ;
Metzler-Northrup, J ;
Lein, P ;
Rueger, D ;
Higgins, D .
DEVELOPMENTAL BRAIN RESEARCH, 1997, 104 (1-2) :101-110
[38]   Initiation of Smad-dependent and Smad-independent signaling via distinct BMP-receptor complexes [J].
Hassel, S ;
Schmitt, S ;
Hartung, A ;
Roth, M ;
Nohe, A ;
Petersen, N ;
Ehrlich, M ;
Henis, YI ;
Sebald, W ;
Knaus, P .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 2003, 85A :44-51
[39]   BMP signaling is required locally to pattern the dorsal telencephalic midline [J].
Hébert, JM ;
Mishina, Y ;
McConnell, SK .
NEURON, 2002, 35 (06) :1029-1041
[40]   FRAP/mTOR is required for proliferation and patterning during embryonic development in the mouse [J].
Hentges, KE ;
Sirry, B ;
Gingras, AC ;
Sarbassov, D ;
Sonenberg, N ;
Sabatini, D ;
Peterson, AS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (24) :13796-13801