Kuruvilla R, Ye H, Ginty D D
Howard Hughes Medical Institute, Department of Neuroscience, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
Neuron. 2000 Sep;27(3):499-512. doi: 10.1016/s0896-6273(00)00061-1.
NGF is a target-derived growth factor for developing sympathetic neurons. Here, we show that application of NGF exclusively to distal axons of sympathetic neurons leads to an increase in PI3-K signaling in both distal axons and cell bodies. In addition, there is a more critical dependence on PI3-K for survival of neurons supported by NGF acting exclusively on distal axons as compared to neurons supported by NGF acting directly on cell bodies. Interestingly, PI3-K signaling within both cell bodies and distal axons contributes to survival of neurons. The requirement for PI3-K signaling in distal axons for survival may be explained by the finding that inhibition of PI3-K in the distal axons attenuates retrograde signaling. Therefore, a single TrkA effector, PI3-K, has multiple roles within spatially distinct cellular locales during retrograde NGF signaling.
神经生长因子(NGF)是发育中的交感神经元的一种靶源性生长因子。在此,我们表明,仅将NGF应用于交感神经元的远端轴突会导致远端轴突和细胞体中的PI3-K信号增加。此外,与NGF直接作用于细胞体所支持的神经元相比,仅作用于远端轴突的NGF所支持的神经元对PI3-K的生存依赖性更强。有趣的是,细胞体和远端轴突内的PI3-K信号都有助于神经元的存活。远端轴突中PI3-K信号对生存的需求可能可以通过以下发现来解释:抑制远端轴突中的PI3-K会减弱逆行信号传导。因此,单一的TrkA效应器PI3-K在逆行NGF信号传导过程中,在空间上不同的细胞区域内具有多种作用。