The p110beta isoform of phosphoinositide 3-kinase signals downstream of G protein-coupled receptors and is functionally redundant with p110gamma

Julie Guillermet-Guibert, Katja Bjorklof, Ashreena Salpekar, Cristiano Gonella, Faruk Ramadani, Antonio Bilancio, Stephen Meek, Andrew J H Smith, Klaus Okkenhaug, Bart Vanhaesebroeck

Research output: Contribution to journalArticlepeer-review


The p110 isoforms of phosphoinositide 3-kinase (PI3K) are acutely regulated by extracellular stimuli. The class IA PI3K catalytic subunits (p110alpha, p110beta, and p110delta) occur in complex with a Src homology 2 (SH2) domain-containing p85 regulatory subunit, which has been shown to link p110alpha and p110delta to Tyr kinase signaling pathways. The p84/p101 regulatory subunits of the p110gamma class IB PI3K lack SH2 domains and instead couple p110gamma to G protein-coupled receptors (GPCRs). Here, we show, using small-molecule inhibitors with selectivity for p110beta and cells derived from a p110beta-deficient mouse line, that p110beta is not a major effector of Tyr kinase signaling but couples to GPCRs. In macrophages, both p110beta and p110gamma contributed to Akt activation induced by the GPCR agonist complement 5a, but not by the Tyr kinase ligand colony-stimulating factor-1. In fibroblasts, which express p110beta but not p110gamma, p110beta mediated Akt activation by the GPCR ligands stromal cell-derived factor, sphingosine-1-phosphate, and lysophosphatidic acid but not by the Tyr kinase ligands PDGF, insulin, and insulin-like growth factor 1. Introduction of p110gamma in these cells reduced the contribution of p110beta to GPCR signaling. Taken together, these data show that p110beta and p110gamma can couple redundantly to the same GPCR agonists. p110beta, which shows a much broader tissue distribution than the leukocyte-restricted p110gamma, could thus provide a conduit for GPCR-linked PI3K signaling in the many cell types where p110gamma expression is low or absent.
Original languageEnglish
Pages (from-to)8292-7
Number of pages6
JournalProceedings of the National Academy of Sciences
Issue number24
Publication statusPublished - Jun 2008


  • Animals
  • Class I Phosphatidylinositol 3-Kinases
  • Complement C5a/pharmacology
  • Fibroblasts/enzymology
  • Genetic Complementation Test
  • Isoenzymes/genetics
  • Isoenzymes/metabolism
  • Ligands
  • Macrophage Colony-Stimulating Factor/pharmacology
  • Macrophages/enzymology
  • Mice
  • Mice, Mutant Strains
  • Phosphatidylinositol 3-Kinases/genetics
  • Phosphatidylinositol 3-Kinases/metabolism
  • Proto-Oncogene Proteins c-akt/metabolism
  • Receptors, G-Protein-Coupled/agonists
  • Receptors, G-Protein-Coupled/metabolism
  • Signal Transduction

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