Dobrowsky R T, Werner M H, Castellino A M, Chao M V, Hannun Y A
Departments of Medicine and Cell Biology, Duke University Medical Center, Durham, NC 27710.
Science. 1994 Sep 9;265(5178):1596-9. doi: 10.1126/science.8079174.
The role of the low-affinity neurotrophin receptor (p75NTR) in signal transduction is undefined. Nerve growth factor can activate the sphingomyelin cycle, generating the putative-lipid second messenger ceramide. In T9 glioma cells, addition of a cell-permeable ceramide analog mimicked the effects of nerve growth factor on cell growth inhibition and process formation. This signaling pathway appears to be mediated by p75NTR in T9 cells and NIH 3T3 cells overexpressing p75NTR. Expression of an epidermal growth factor receptor-p75NTR chimera in T9 cells imparted to epidermal growth factor the ability to activate the sphingomyelin cycle. These data demonstrate that p75NTR is capable of signaling independently of the trk neurotrophin receptor (p140trk) and that ceramide may be a mediator in neurotrophin biology.
低亲和力神经营养因子受体(p75NTR)在信号转导中的作用尚不清楚。神经生长因子可激活鞘磷脂循环,生成假定的脂质第二信使神经酰胺。在T9胶质瘤细胞中,添加可穿透细胞的神经酰胺类似物可模拟神经生长因子对细胞生长抑制和突起形成的作用。在T9细胞和过表达p75NTR的NIH 3T3细胞中,该信号通路似乎由p75NTR介导。在T9细胞中表达表皮生长因子受体-p75NTR嵌合体赋予表皮生长因子激活鞘磷脂循环的能力。这些数据表明,p75NTR能够独立于trk神经营养因子受体(p140trk)进行信号传导,并且神经酰胺可能是神经营养因子生物学中的一种介质。