Gene interactions and pathways from curated databases and text-mining

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NGF — RHOA

Pathways - manually collected, often from reviews:

Text-mined interactions from Literome

Yamaguchi et al., J Biol Chem 2001 : NGF induced a rapid activation of Rac1 and suppression of RhoA activity
Liu et al., Mol Cell Neurosci 2002 : Inhibition of the small GTPase RhoA by the dominant negative mutant RhoA ( T19N ) restored NGF responsiveness of axon growth on L1 to Bax ( -/- ) neurons
Nusser et al., J Biol Chem 2002 : The inhibitory pathway from TrkA to RhoA involves phosphatidylinositol-3-kinase (PI3K), because the inhibitors LY294002 or wortmannin prevented NGF induced RhoA translocation and increased RhoA association with ROK
Nusser et al., Cell Signal 2006 : However, when monitoring NGF induced binding of GTP-RhoA to multiple targets, we noted differential interactions with its effectors ... In the context of PC12 cell differentiation, NGF induced phosphorylation of RhoA on serine ( 188 ) prevents it from interacting with ROK, which would otherwise block neurite outgrowth
Noga et al., Clin Exp Allergy 2007 (Hypersensitivity) : NGF led to decreased RhoA and increased Rac activation, while BDNF affected RhoA and Rac activity in a reciprocal fashion
Jeon et al., Exp Mol Med 2010 : p190RhoGAP and Rap dependent RhoGAP ( ARAP3 ) inactivate RhoA in response to nerve growth factor leading to neurite outgrowth from PC12 cells ... NGF suppressed GTP-RhoA levels after 12 h in PC12 cells and was consistently required for a long time to induce neurite outgrowth ... Constitutively active ( CA ) -RhoA suppressed neurite outgrowth from PC12 cells in response to NGF , whereas dominant negative ( DN ) -RhoA stimulated it, suggesting that RhoA inactivation is essential for neurite outgrowth ... DN-p190RhoGAP abrogated neurite outgrowth, whereas wild-type ( WT ) -p190RhoGAP and WT-Src synergistically stimulated it along with accelerating RhoA inactivation, suggesting that p190RhoGAP, which can be activated by Src, is a major component in inhibiting RhoA in response to NGF in PC12 cells