Kuner P, Hertel C
F. Hoffmann-LaRoche Ltd., Pharma Division, Preclinical Research, Basel, Switzerland.
J Neurosci Res. 1998 Nov 15;54(4):465-74. doi: 10.1002/(SICI)1097-4547(19981115)54:4<465::AID-JNR4>3.0.CO;2-T.
Nerve growth factor (NGF) has been demonstrated to support survival and differentiation of neuronal cells. Recently, a role of NGF in neuronal apoptosis has been suggested. NGF binds to tropomyosin receptor kinase A (TrkA) and to 75-kDa NGF receptor (p75NTR). TrkA is responsible for differentiation and survival, but p75NTR, a member of the death receptor family, seems to mediate the apoptotic effect of NGF. Here we demonstrate that NGF-but not neurotrophin-3 (NT-3) or brain-derived neurotrophic factor (BDNF)-induced apoptosis in p75NTR-expressing human neuroblastoma SK-N-MC cells. BDNF prevented NGF-induced apoptosis. NGF-induced apoptosis was accompanied by the release of NFkappaB p65 and the activation of stress-activated protein kinase/c-jun amino terminal kinase. Because p75NTR and NGF are upregulated in Alzheimer's disease, NGF/p75NTR might be involved in neuronal cell death related to the disease.
神经生长因子(NGF)已被证明可支持神经元细胞的存活和分化。最近,有人提出NGF在神经元凋亡中发挥作用。NGF与原肌球蛋白受体激酶A(TrkA)以及75 kDa的NGF受体(p75NTR)结合。TrkA负责细胞分化和存活,但p75NTR作为死亡受体家族的一员,似乎介导了NGF的凋亡效应。在此我们证明,在表达p75NTR的人神经母细胞瘤SK-N-MC细胞中,NGF可诱导凋亡,而神经营养因子-3(NT-3)或脑源性神经营养因子(BDNF)则不会。BDNF可阻止NGF诱导的凋亡。NGF诱导的凋亡伴随着NFκB p65的释放以及应激激活蛋白激酶/c-Jun氨基末端激酶的激活。由于在阿尔茨海默病中p75NTR和NGF上调,NGF/p75NTR可能参与了与该疾病相关的神经元细胞死亡。