Dechant G, Barde Y A
Max-Planck Institute for Psychiatry, Department of Neurobiochemistry Am Klopferspitz 18A, 82152 Martinsried, Germany.
Curr Opin Neurobiol. 1997 Jun;7(3):413-8. doi: 10.1016/s0959-4388(97)80071-2.
Activation specific tyrosine kinase receptors by neurotrophins accounts for the longest known biological actions of the neurotrophins, in particular the promotion of neuronal survival. However, recent studies have revealed that nerve growth factor, the neurotrophin regarded as best understood, also activates a signalling pathway by binding to the neurotrophin receptor p75(NTR). This receptor belongs to the tumor necrosis factor receptor family and lacks intrinsic catalytic activity. The p75(NTR) receptor binds all neurotrophins with nanomolar affinity; however, nerve growth factor seems to be uniquely able to activate it, causing the death of trkA-negative neurons during normal development. Thus, nerve growth factor prevents programmed cell death through its receptor TrkA, but promotes it by signalling through p75(NTR).
神经营养因子对特定酪氨酸激酶受体的激活介导了神经营养因子最长已知的生物学作用,特别是促进神经元存活。然而,最近的研究表明,神经生长因子,这种被认为了解最透彻的神经营养因子,也通过与神经营养因子受体p75(NTR)结合来激活一条信号通路。该受体属于肿瘤坏死因子受体家族,缺乏内在催化活性。p75(NTR)受体以纳摩尔亲和力结合所有神经营养因子;然而,神经生长因子似乎具有独特的激活能力,在正常发育过程中导致trkA阴性神经元死亡。因此,神经生长因子通过其受体TrkA防止程序性细胞死亡,但通过p75(NTR)发出信号促进细胞死亡。