Publication | Open Access
High Density Lipoprotein-induced Signaling of the MAPK Pathway Involves Scavenger Receptor Type BI-mediated Activation of Ras
79
Citations
23
References
2003
Year
Pertussis ToxinMolecular PhysiologySignal TransductionCell RegulationG Protein-coupled ReceptorNutrient SignallingHigh Density LipoproteinMedicineImmunologyReceptor Tyrosine KinaseSignaling PathwayMapk PathwayReceptor Type BiLipoprotein MetabolismPharmacologyCell BiologyCell SignalingMolecular Signaling
High density lipoprotein (HDL) stimulates multiple signaling pathways. HDL-induced activation of the mitogen-activated protein kinase (MAPK) pathway can be mediated by protein kinase C (PKC) and/or pertussis toxin-sensitive G-proteins. Although HDL-induced activation of MAPK involves Raf-1, Mek, and Erk1/2, the upstream contribution of p21(ras) (Ras) on the activation of Raf-1 and MAPK remains elusive. Here we examine the effect of HDL on Ras activity and demonstrate that HDL induces PKC-independent activation of Ras that is completely blocked by pertussis toxin, thus implicating heterotrimeric G-proteins. In addition, the HDL-induced activation of Ras is inhibited by a neutralizing antibody against scavenger receptor type BI. We conclude that the binding of HDL to scavenger receptor type BI activates Ras in a PKC-independent manner with subsequent induction of the MAPK signaling cascade.
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