Spatially and functionally distinct roles of the PI3-K effector pathway during NGF signaling in sympathetic neurons

被引:189
|
作者
Kuruvilla, R [1 ]
Ye, HH [1 ]
Ginty, DD [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Howard Hughes Med Inst, Dept Neurosci, Baltimore, MD 21205 USA
关键词
D O I
10.1016/S0896-6273(00)00061-1
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
引用
收藏
页码:499 / 512
页数:14
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