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Publication : Antagonistic regulation of neurite morphology through Gq/G11 and G12/G13.

First Author  Nürnberg A Year  2008
Journal  J Biol Chem Volume  283
Issue  51 Pages  35526-31
PubMed ID  18854320 Mgi Jnum  J:144584
Mgi Id  MGI:3831243 Doi  10.1074/jbc.M804972200
Citation  Nurnberg A, et al. (2008) Antagonistic regulation of neurite morphology through Gq/G11 and G12/G13. J Biol Chem 283(51):35526-31
abstractText  The induction of neurite retraction and growth cone collapse via G-protein-coupled receptors is involved in developmental as well as regenerative processes. The role of individual G-protein-mediated signaling processes in the regulation of neurite morphology is still incompletely understood. Using primary neurons from brains lacking Galpha(q)/Galpha(11) or Galpha(12)/Galpha(13), we show here that G(12)/G(13)-mediated signaling is absolutely required for neurite retraction and growth cone collapse induced by the blood-borne factors lysophosphatidic acid and thrombin. Interestingly, the effects of lysophosphatidic acid were mediated mainly by G(13), whereas thrombin effects required G(12). Surprisingly, lack of Galpha(q)/Galpha(11) resulted in overshooting responses to both stimuli, indicating that G(q)/G(11)-mediated signaling most likely via activation of Rac antagonizes the effects of G(12)/G(13).
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