Exogenous and fibroblast growth factor 2/epidermal growth factor-regulated endogenous cytokines regulate neural precursor cell growth and differentiation

被引:51
作者
Deleyrolle, Loic [1 ]
Marchal-Victorion, Sophie [1 ]
Dromard, Cecile [1 ]
Fritz, Vanessa [1 ]
Saunier, Monique [1 ]
Sabourin, Jean-Charles [1 ]
Van Ba, Christophe Tran [1 ]
Privat, Alain [1 ]
Hugnot, Jean-Philippe [1 ]
机构
[1] Hop St Eloi, INM, INSERM, U583,Inst Neurosci Montpellier, F-34295 Montpellier, France
关键词
neural stem cells; spinal cord; cytokines; growth differentiation; astrocytes; gene array; knockout;
D O I
10.1634/stemcells.2005-0138
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Neurospheres (NSs) are clonal cellular aggregates composed of neural stem cells and progenitors. A comprehensive description of their proliferation and differentiation regulation is an essential prerequisite for their use in biotherapies. Cytokines are essential molecules regulating cell precursor fate. Using a gene-array strategy, we conducted a descriptive and functional analysis of endogenous cytokines; and receptors expressed by spinal cord-derived NSs during their growth or their differentiation into neuronal and glial cells. NSs were found to express approximately 100 receptor subunits and cytokine/secreted developmental factors. Several angiogenic factors and receptors that could mediate neural precursor cell-endothelial cell relationships were detected. Among them, receptor B for endothelins was highly expressed, and endothelins were found to increase NS growth. In contrast, NSs express receptors for ciliary neurotrophic factor (CNTF), bone morphogenetic protein (BMP), interferon (IFN)-gamma, or tumor necrosis factor (TNF)-alpha, which, when added in the growth phase, led to a dramatic growth reduction followed by a reduction or a loss of oligodendrocyte formation on differentiation. In addition, NSs synthesize fibroblast growth factor 2/epidermal growth factor (FGF2/EGF)-regulated endogenous cytokines that participate in their growth and differentiation. Notably, BMP-7 and CNTF were expressed during expansion, but upon differentiation there was a remarkable switch from BMP-7 to BMP-4 and -6 and a sharp increase of CNTF. Reintroduction of growth factors reverses the BMP expression profile, indicating growth factor-BMP cross-regulations. The role of endogenous CNTF was investigated by deriving NSs from CNTF knockout mice. These NSs have an increased growth rate associated with reduction of apoptosis and generate astrocytes with a reduced glial fibulary acidic protein (GFAP) content. These results demonstrate the combined role of endogenous and exogenous cytokines in neural precursor cell growth and differentiation.
引用
收藏
页码:748 / 762
页数:15
相关论文
共 98 条
[51]   DISRUPTION OF THE CNTF GENE RESULTS IN MOTOR-NEURON DEGENERATION [J].
MASU, Y ;
WOLF, E ;
HOLTMANN, B ;
SENDTNER, M ;
BREM, G ;
THOENEN, H .
NATURE, 1993, 365 (6441) :27-32
[52]  
Mekki-Dauriac S, 2002, DEVELOPMENT, V129, P5117
[53]   STAT3 activation is a critical step in gp130-mediated terminal differentiation and growth arrest of a myeloid cell line [J].
Minami, M ;
Inoue, M ;
Wei, S ;
Takeda, K ;
Matsumoto, M ;
Kishimoto, T ;
Akira, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (09) :3963-3966
[54]   Inflammatory blockade restores adult hippocampal neurogenesis [J].
Monje, ML ;
Toda, H ;
Palmer, TD .
SCIENCE, 2003, 302 (5651) :1760-1765
[55]   Irradiation induces neural precursor-cell dysfunction [J].
Monje, ML ;
Mizumatsu, S ;
Fike, JR ;
Palmer, TD .
NATURE MEDICINE, 2002, 8 (09) :955-962
[56]  
Morrow T, 2001, DEVELOPMENT, V128, P3585
[57]   Endothelin and the central and peripheral nervous systems: A decade of endothelin research [J].
Mortensen, LH .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 1999, 26 (12) :980-984
[58]  
Nakashima K, 2002, MOL NEUROBIOL, V25, P233
[59]   Neural stem cells display an inherent mechanism for rescuing dysfunctional neurons [J].
Ourednik, J ;
Ourednik, V ;
Lynch, WP ;
Schachner, M ;
Snyder, EY .
NATURE BIOTECHNOLOGY, 2002, 20 (11) :1103-1110
[60]  
Palmer TD, 2000, J COMP NEUROL, V425, P479, DOI 10.1002/1096-9861(20001002)425:4<479::AID-CNE2>3.0.CO