β-arrestin 1 couples thrombin to the rapid activation of the Akt pathway

Reema Goel, Joseph J. Baldassare

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

Abstract

In a variety of cell types including chinese hamster embryonic fibroblasts (IIC9 cells), α-thrombin is a potent mitogen. Thrombin irreversibly activates Par 1, a member of the seven membrane-spanning superfamily of G protein-coupled receptors (GPCRs). This, in turn, activates several heterotrimeric G proteins and induces signaling pathways that are critical for cell cycle reentry and proliferation. In IIC9 cells, α-thrombin activates the phosphatidylinositol-3-OH kinase (PI 3-Kinase)/Akt pathway, which is essential for G1 cell cycle progression. At present the mechanism for activation and regulation of the PI 3-kinase/Akt pathway is not fully understood. My preliminary data demonstrates a role for β-arrestin 1 in the regulation of α-thrombin-induced Akt activity. In addition to their importance in receptor down-regulation, β-arrestins are now known to scaffold proteins involved in stimulating specific signaling pathways. My preliminary data show that <-thrombin activates a rapid Akt activity in a β-arrestin 1-dependent manner in IIC9 cells.

Original languageEnglish (US)
Pages (from-to)138-141
Number of pages4
JournalAnnals of the New York Academy of Sciences
Volume973
DOIs
StatePublished - Jan 1 2002

All Science Journal Classification (ASJC) codes

  • Neuroscience(all)
  • Biochemistry, Genetics and Molecular Biology(all)
  • History and Philosophy of Science

Fingerprint Dive into the research topics of 'β-arrestin 1 couples thrombin to the rapid activation of the Akt pathway'. Together they form a unique fingerprint.

Cite this