PDGF enhances store-operated caspi 2+ entry by upregulating stim1/orai1 via activation of Akt/mTOR in human pulmonary arterial smooth muscle cells

Aiko Ogawa, Amy L. Firth, Kimberly A. Smith, Mary V. Maliakal, Yuan J. Jason

Research output: Contribution to journalArticlepeer-review

63 Scopus citations

Abstract

Plateletderived growth factor (PDGF) and its receptor are known to be substantially elevated in lung tissues and pulmonary arterial smooth muscle cells (PASMC) isolated from patients and animals with pulmonary arterial hypertension. PDGF has been shown to phosphorylate and activate Akt and mammalian target of rapamycin (mTOR) in PASMC. In this study, we investigated the role of PDGF-mediated activation of Akt signaling in the regulation of cytosolic Ca 2+ concentration and cell proliferation. PDGF activated the Akt/mTOR pathway and, subsequently, enhanced store-operated Ca 2+ entry (SOCE) and cell proliferation in human PASMC. Inhibition of Akt attenuated the increase in cytosolic Ca 2+ concentration due to both SOCE and PASMC proliferation. This effect correlated with a significant downregulation of stromal interacting molecule (STIM) and Orai, proposed molecular correlates for SOCE in many cell types. The data from this study present a novel pathway for the regulation of Ca 2+ signaling and PASMC proliferation involving activation of Akt in response to upregulated expression of PDGF. Targeting this pathway may lead to the development of a novel therapeutic option for the treatment of pulmonary arterial hypertension.

Original languageEnglish (US)
Pages (from-to)C405-C411
JournalAmerican Journal of Physiology - Cell Physiology
Volume302
Issue number2
DOIs
StatePublished - Jan 2012

Keywords

  • Akt/mammalian target of rapamycin pathway
  • Platelet-derived growth factor
  • Pulmonary vascular remodeling
  • Store-operated caspi entry

ASJC Scopus subject areas

  • Physiology
  • Cell Biology

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