[PDF][PDF] NGF-induced axon growth is mediated by localized inactivation of GSK-3β and functions of the microtubule plus end binding protein APC

FQ Zhou, J Zhou, S Dedhar, YH Wu, WD Snider - Neuron, 2004 - cell.com
FQ Zhou, J Zhou, S Dedhar, YH Wu, WD Snider
Neuron, 2004cell.com
Little is known about how nerve growth factor (NGF) signaling controls the regulated
assembly of microtubules that underlies axon growth. Here we demonstrate that a tightly
regulated and localized activation of phosphatidylinositol 3-kinase (PI3K) at the growth cone
is essential for rapid axon growth induced by NGF. This spatially activated PI3K signaling is
conveyed downstream through a localized inactivation of glycogen synthase kinase 3β
(GSK-3β). These two spatially coupled kinases control axon growth via regulation of a …
Abstract
Little is known about how nerve growth factor (NGF) signaling controls the regulated assembly of microtubules that underlies axon growth. Here we demonstrate that a tightly regulated and localized activation of phosphatidylinositol 3-kinase (PI3K) at the growth cone is essential for rapid axon growth induced by NGF. This spatially activated PI3K signaling is conveyed downstream through a localized inactivation of glycogen synthase kinase 3β (GSK-3β). These two spatially coupled kinases control axon growth via regulation of a microtubule plus end binding protein, adenomatous polyposis coli (APC). Our results demonstrate that NGF signals are transduced to the axon cytoskeleton via activation of a conserved cell polarity signaling pathway.
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