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低亲和力神经生长因子受体诱导细胞凋亡

Induction of apoptosis by the low-affinity NGF receptor.

作者信息

Rabizadeh S, Oh J, Zhong L T, Yang J, Bitler C M, Butcher L L, Bredesen D E

机构信息

Department of Neurology, University of California, Los Angeles 90024.

出版信息

Science. 1993 Jul 16;261(5119):345-8. doi: 10.1126/science.8332899.

Abstract

Nerve growth factor (NGF) binding to cellular receptors is required for the survival of some neural cells. In contrast to TrkA, the high-affinity NGF receptor that transduces NGF signals for survival and differentiation, the function of the low-affinity NGF receptor, p75NGFR, remains uncertain. Expression of p75NGFR induced neural cell death constitutively when p75NGFR was unbound; binding by NGF or monoclonal antibody, however, inhibited cell death induced by p75NGFR. Thus, expression of p75NGFR may explain the dependence of some neural cells on NGF for survival. These findings also suggest that p75NGFR has some functional similarities to other members of a superfamily of receptors that include tumor necrosis factor receptors, Fas (Apo-1), and CD40.

摘要

某些神经细胞的存活需要神经生长因子(NGF)与细胞受体结合。与转导NGF信号以实现存活和分化的高亲和力NGF受体TrkA不同,低亲和力NGF受体p75NGFR的功能仍不确定。当p75NGFR未结合时,其表达会持续诱导神经细胞死亡;然而,NGF或单克隆抗体的结合会抑制p75NGFR诱导的细胞死亡。因此,p75NGFR的表达可能解释了一些神经细胞对NGF存活的依赖性。这些发现还表明,p75NGFR与包括肿瘤坏死因子受体、Fas(Apo-1)和CD40在内的受体超家族的其他成员具有一些功能相似性。

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