Role of the phosphatidylinositol-3-kinase and extracellular regulated kinase pathways in the induction of hypoxia-inducible factor (HIF)-1 activity and the HIF-1 target vascular endothelial growth factor in ovarian granulosa cells in response to follicle-stimulating hormone

Hena Alam, Jennifer Week, Evelyn Maizels, Youngkyu Park, Eun Jig Lee, Margaret Ashcroft, Mary Hunzicker-Dunn

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FSH stimulation of granulosa cells (GCs) results in increased hypoxia-inducible factor (HIF)-1α protein levels and HIF-1 activity that is necessary for up-regulation of certain FSH target genes including vascular endothelial growth factor. We report that the role of the phosphatidylinositol (PI)-3-kinase/AKT pathway in increasing HIF-1 α protein in FSH-stimulated GCs extends beyond an increase in mammalian target of rapamycin-stimulated translation. FSH increases phosphorylation of the AKT target mouse double-minute 2 (MDM2); a phosphomimetic mutation of MDM2 is sufficient to induce HIF-1 activity. The PI3-kinase/AKT target forkhead box-containing protein O subfamily 1 (FOXO1) also effects the accumulation of HIF-1α as evidenced by the ability of a constitutively active FOXO1 mutant to inhibit the induction by FSH of HIF-1 α protein and HIF-1 activity. Activation of the PI3-kinase/AKT pathway in GCs by IGF-I is sufficient to induce HIF-1 α protein but surprisingly not HIF-1 activity. HIF-1 activity also appearsto require a PD98059-sensitive protein (kinase) activity stimulated by FSH that is both distinct from mitogen-activated ERK kinase1/2 or 5 and independent of the PI3-kinase/AKT pathway. These results indicate that FSH-stimulated HIF-1 activation leadingto up-regulation of targetssuch asvascularendothelial growth factor requires not only PI3-kinase/AKT-mediated activation of mammalian target of rapamycin as well as phosphorylation of FOXO1 and possibly MDM2 but also a protein (kinase) activity that is inhibited by the classic ERK kinase inhibitor PD98059 but not ERK1/2 or 5. Thus, regulation of HIF-1 activity in GCs by FSH under normoxic conditions is complex and requires input from multiple signaling pathways.

Original languageEnglish
Pages (from-to)915-928
Number of pages14
Issue number2
Publication statusPublished - 2009 Feb 1


All Science Journal Classification (ASJC) codes

  • Endocrinology

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