What role(s) for TGFα in the central nervous system?

被引:98
作者
Junier, MP [1 ]
机构
[1] Fac Med, INSERM, U421, F-94010 Creteil, France
关键词
TGF alpha; EGF; erbB1; EGFR; astrocyte; astrogliosis; neurodegenerative disease; neural progenitor; astrocytoma; glioma;
D O I
10.1016/S0301-0082(00)00017-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Transforming growth factor alpha (TGF alpha) is a member of the epidermal growth factor (EGF) family with which it shares the same receptor, the EGF receptor (EGFR or erbB1). Identified since 1985 in the central nervous system (CNS), its functions in this organ have started to be determined during the past decade although numerous questions remain unanswered. TGF alpha is widely distributed in the nervous system, both glial and neuronal cells contributing to its synthesis. Although astrocytes appear as its main targets, mediating in part TGF alpha. effects on different neuronal populations, results from different studies have raised the possibility for a direct action of this growth factor on neurons. A large array of experimental data have thus pointed to TGF alpha as a multifunctional factor in the CNS. This review is an attempt to present, in a comprehensive manner, the very diverse works performed in vitro and in vivo which have provided evidences for (i) an intervention of TGF alpha in the control of developmental events such as neural progenitors proliferation/cell fate choice, neuronal survival/differentiation, and neuronal control of female puberty onset, (ii) its role as a potent regulator of astroglial metabolism including astrocytic reactivity, (iii) its neuroprotective potential, and (iv) its participation to neuropathological processes as exemplified by astroglial neoplasia. In addition, informations regarding the complex modes of TGF alpha action at the molecular level are provided, and its place within the large EGF family is precised with regard to the potential interactions and substitutions which may take place between TGF alpha and its kindred. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:443 / 473
页数:31
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