HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Coupling of mitochondria to store-operated Ca(2+)-signaling sustains constitutive activation of protein kinase B/Akt and augments survival of malignant melanoma cells.

Abstract
Mitochondria are emerging as a major hub for cellular Ca(2+)-signaling, though their contribution to Ca(2+)-driven growth- and survival-promoting events in cancer is poorly understood. Here employing flow cytometry to monitor mitochondrial and cytosolic Ca(2+), we assessed trans-mitochondrial Ca(2+)-transport and store-operated Ca(2+)-influx (store-operated channels (SOC)) in malignant vs. non-malignant B16BL6 melanoma clones. Remarkably, mitochondrial Ca(2+)-fluxes measured in whole cells or in isolated mitochondria were accelerated in the malignant clones compared to their non-malignant counterpart clones. This coincided with enhanced SOC-mediated Ca(2+)-influx and high levels of constitutively active protein kinase B/Akt (PKB). Interruption of trans-mitochondrial Ca(2+)-transport in the malignant cells with an antagonist of the mitochondrial Na(+)/Ca(2+) exchanger, CGP-37157, abolsihed SOC-mediated Ca(2+)-influx, inactivated PKB, retarded cell growth and increased vulnerability to apoptosis. Similarly, direct SOC blockade by silencing Stim1 inhibited PKB, indicating that the crosstalk between SOC and mitochondria is essential to preserve PKB in constitutively active state. Finally, the retraction of mitochondria from sub-plasmalemmal micro-domains triggered by Fis1 over-expression inhibited SOC-coupled trans-mitochondrial Ca(2+)-flux, Ca(2+)-entry via SOC and PKB activity. Taken together, our data show that in the malignant melanoma cells, the functional and spatial relationship of up-regulated mitochondrial Ca(2+)-transport to the SOC sustains the robust Ca(2+)-responses and down-stream signaling critical for apoptosis-resistance and proliferation.
AuthorsBen Feldman, Shlomit Fedida-Metula, Julia Nita, Israel Sekler, Daniel Fishman
JournalCell calcium (Cell Calcium) Vol. 47 Issue 6 Pg. 525-37 (Jun 2010) ISSN: 1532-1991 [Electronic] Netherlands
PMID20605628 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Copyright2010 Elsevier Ltd. All rights reserved.
Chemical References
  • Calcium Channels
  • Sodium-Calcium Exchanger
  • Thiazepines
  • Clonazepam
  • CGP 37157
  • Proto-Oncogene Proteins c-akt
  • Calcium
Topics
  • Animals
  • Calcium (metabolism)
  • Calcium Channels (metabolism)
  • Calcium Signaling
  • Cell Survival
  • Clonazepam (analogs & derivatives, pharmacology)
  • Flow Cytometry
  • Melanoma (enzymology, metabolism)
  • Mice
  • Mitochondria (metabolism)
  • Proto-Oncogene Proteins c-akt (metabolism)
  • Sodium-Calcium Exchanger (antagonists & inhibitors, metabolism)
  • Thiazepines (pharmacology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: