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神经营养因子:引发细胞凋亡的生存因子的生物学悖论。

Neurotrophins: the biological paradox of survival factors eliciting apoptosis.

作者信息

Casaccia-Bonnefil P, Kong H, Chao M V

机构信息

Molecular Neurobiology Program, Skirball Institute, 540 First Avenue, New York, USA 10016, USA.

出版信息

Cell Death Differ. 1998 May;5(5):357-64. doi: 10.1038/sj.cdd.4400377.

Abstract

Neurotrophins are target-derived soluble polypeptides required for neuronal survival. Binding of neurotrophins to Trk receptor tyrosine kinases initiate signaling cascades that promote cell survival and differentiation. All family members bind to another receptor (p75NTR), which belongs to the tumor necrosis factor superfamily. Hence, nerve growth factor (NGF) and related trophic factors are unique in that two separate receptor types are utilized. Although the biological function of p75NTR has been elusive, it has been suggested to mediate apoptosis of developing neurons in the absence of Trk receptors. This presents a tantalizing paradigm, in which life-death decisions of cells are dependent upon the expression and action of two different receptors with distinctive signaling mechanisms. In the presence of TrkA receptors, p75 can participate in the formation of high affinity binding sites and enhanced NGF responsiveness leading to a survival signal. In the absence of TrkA receptors, p75 can generate, in only specific cell populations, a death signal. Here we discuss the unique features and implications of this unusual signal transduction system.

摘要

神经营养因子是神经元存活所需的由靶细胞衍生的可溶性多肽。神经营养因子与Trk受体酪氨酸激酶结合会启动信号级联反应,促进细胞存活和分化。所有家族成员都与另一种受体(p75NTR)结合,该受体属于肿瘤坏死因子超家族。因此,神经生长因子(NGF)和相关的营养因子的独特之处在于它们利用了两种不同的受体类型。尽管p75NTR的生物学功能一直难以捉摸,但有人提出它在没有Trk受体的情况下介导发育中神经元的凋亡。这呈现出一个诱人的范例,即细胞的生死决定取决于具有独特信号机制的两种不同受体的表达和作用。在存在TrkA受体的情况下,p75可以参与高亲和力结合位点的形成并增强NGF反应性,从而产生存活信号。在没有TrkA受体的情况下,p75仅在特定细胞群体中产生死亡信号。在此我们讨论这个不同寻常的信号转导系统的独特特征及其意义。

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