Gβγ subunits inhibit Epac-induced melanoma cell migration

BMC Cancer. 2011 Jun 17:11:256. doi: 10.1186/1471-2407-11-256.

Abstract

Background: Recently we reported that activation of Epac1, an exchange protein activated by cAMP, increases melanoma cell migration via Ca 2+ release from the endoplasmic reticulum (ER). G-protein βγ subunits (Gβγ) are known to act as an independent signaling molecule upon activation of G-protein coupled receptor. However, the role of Gβγ in cell migration and Ca 2+ signaling in melanoma has not been well studied. Here we report that there is crosstalk of Ca 2+ signaling between Gβγ and Epac in melanoma, which plays a role in regulation of cell migration.

Methods: SK-Mel-2 cells, a human metastatic melanoma cell line, were mainly used in this study. Intracellular Ca 2+ was measured with Fluo-4AM fluorescent dyes. Cell migration was examined using the Boyden chambers.

Results: The effect of Gβγ on Epac-induced cell migration was first examined. Epac-induced cell migration was inhibited by mSIRK, a Gβγ -activating peptide, but not its inactive analog, L9A, in SK-Mel-2 cells. Guanosine 5', α-β-methylene triphosphate (Gp(CH2)pp), a constitutively active GTP analogue that activates Gβγ, also inhibited Epac-induced cell migration. In addition, co-overexpression of β1 and γ2, which is the major combination of Gβγ, inhibited Epac1-induced cell migration. By contrast, when the C-terminus of β adrenergic receptor kinase (βARK-CT), an endogenous inhibitor for Gβγ, was overexpressed, mSIRK's inhibitory effect on Epac-induced cell migration was negated, suggesting the specificity of mSIRK for Gβγ. We next examined the effect of mSIRK on Epac-induced Ca 2+ response. When cells were pretreated with mSIRK, but not with L9A, 8-(4-Methoxyphenylthio)-2'-O-methyladenosine-3',5'-cyclic monophosphate (8-pMeOPT), an Epac-specific agonist, failed to increase Ca 2+ signal. Co-overexpression of β1 and γ2 subunits inhibited 8-pMeOPT-induced Ca 2+ elevation. Inhibition of Gβγ with βARK-CT or guanosine 5'-O-(2-thiodiphosphate) (GDPβS), a GDP analogue that inactivates Gβγ, restored 8-pMeOPT-induced Ca 2+ elevation even in the presence of mSIRK. These data suggested that Gβγ inhibits Epac-induced Ca 2+ elevation. Subsequently, the mechanism by which Gβγ inhibits Epac-induced Ca 2+ elevation was explored. mSIRK activates Ca 2+ influx from the extracellular space. In addition, W-5, an inhibitor of calmodulin, abolished mSIRK's inhibitory effects on Epac-induced Ca 2+ elevation, and cell migration. These data suggest that, the mSIRK-induced Ca 2+ from the extracellular space inhibits the Epac-induced Ca 2+ release from the ER, resulting suppression of cell migration.

Conclusion: We found the cross talk of Ca 2+ signaling between Gβγ and Epac, which plays a major role in melanoma cell migration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Calcium Channel Blockers / pharmacology
  • Calcium Signaling / physiology*
  • Calmodulin / physiology
  • Cell Line, Tumor / drug effects
  • Cell Movement / drug effects
  • GTP-Binding Protein beta Subunits / genetics
  • GTP-Binding Protein beta Subunits / physiology*
  • GTP-Binding Proteins / genetics
  • GTP-Binding Proteins / physiology*
  • Guanine Nucleotide Exchange Factors / antagonists & inhibitors*
  • Guanine Nucleotide Exchange Factors / physiology
  • Guanosine Diphosphate / analogs & derivatives
  • Guanosine Diphosphate / pharmacology
  • Guanosine Triphosphate / analogs & derivatives
  • Guanosine Triphosphate / pharmacology
  • Humans
  • Melanoma / pathology*
  • Melanoma / secondary
  • Molecular Sequence Data
  • Neoplasm Proteins / antagonists & inhibitors
  • Neoplasm Proteins / physiology*
  • Peptide Fragments / pharmacology
  • Peptides / pharmacology
  • Recombinant Fusion Proteins / physiology
  • Recombinant Proteins / pharmacology
  • Thionucleotides / pharmacology
  • beta-Adrenergic Receptor Kinases / antagonists & inhibitors

Substances

  • Calcium Channel Blockers
  • Calmodulin
  • GNB1 protein, human
  • GNG2 protein, human
  • GTP-Binding Protein beta Subunits
  • Guanine Nucleotide Exchange Factors
  • Neoplasm Proteins
  • Peptide Fragments
  • Peptides
  • RAPGEF3 protein, human
  • Recombinant Fusion Proteins
  • Recombinant Proteins
  • Thionucleotides
  • beta-adrenergic receptor kinase inhibitory peptide
  • Guanosine Diphosphate
  • guanosine 5'-(alpha,beta-methylene)triphosphate
  • guanosine 5'-O-(2-thiodiphosphate)
  • Guanosine Triphosphate
  • beta-Adrenergic Receptor Kinases
  • GTP-Binding Proteins