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October 1, 1993Journal of Biological Chemistry230 citationsOpen Access

Lysophosphatidic acid stimulates mitogen-activated protein kinase activation via a G-protein-coupled pathway requiring p21ras and p74raf-1.

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LHLouise R. HoweCMC. J. Marshall

Key Points

  • The study aims to clarify the roles of p21ras and p74raf-1 in lysophosphatidic acid-induced MAP kinase activation through G-protein-coupled receptors.
  • Investigated the effect of lysophosphatidic acid on MAP kinase activation.
  • Utilized pertussis toxin-sensitive pathways and dominant negative constructs to analyze the involvement of p21ras and p74raf-1.
  • Overexpressed p74raf-1 and introduced a dominant negative Raf protein to assess their impacts on MAP kinase activation.
  • Lysophosphatidic acid stimulates MAP kinase activation via a pertussis toxin-sensitive pathway.
  • Activation is blocked by dominant negative Ras, confirming the necessity of p21ras.
  • Overexpression of p74raf-1 potentiates MAP kinase activation, while dominant negative Raf inhibits it.

Abstract

Activation of tyrosine kinase receptors causes mitogen-activated protein (MAP) kinase stimulation via a pathway involving p21ras, p74raf-1 (acting as a MAP kinase kinase kinase), and MAP kinase kinases; however, the pathway by which heterotrimeric G-protein-coupled receptors activate MAP kinases is undefined. Since there are several MAP kinase kinase kinases it has been suggested that p74raf-1 may only couple tyrosine kinase receptors to MAP kinase activation. We therefore investigated the requirement for p21ras and p74raf-1 in G-protein receptor-mediated MAP kinase activation. Lysophosphatidic acid stimulates MAP kinase via a pertussis toxin-sensitive pathway, which is blocked by dominant negative Ras. Lysophosphatidic acid-stimulated MAP kinase activation is potentiated by overexpression of p74raf-1 and blocked by expression of a dominant negative Raf protein comprising the N-terminal 259 amino acids. We conclude that lysophosphatidic acid activates MAP kinases by a G-protein-coupled pathway that requires both p21ras and p74raf-1.

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Cite This Study

Howe et al. (1993) studied this question.

synapsesocial.com/papers/6a1970d6001a20a9c0d96e49https://doi.org/10.1016/s0021-9258(19)36838-3
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