| Autor: |
Martinovich GG; Department of Biophysics, Belarusian State University, Nezavisimosti Avenue 4, 220030 Minsk, Belarus., Golubeva EN, Martinovich IV, Cherenkevich SN |
| Jazyk: |
angličtina |
| Zdroj: |
Journal of biophysics (Hindawi Publishing Corporation : Online) [J Biophys] 2012; Vol. 2012, pp. 921653. Date of Electronic Publication: 2012 Nov 25. |
| DOI: |
10.1155/2012/921653 |
| Abstrakt: |
Previously, we have reported that ascorbic acid regulates calcium signaling in human larynx carcinoma HEp-2 cells. To evaluate the precise mechanism of Ca(2+) release by ascorbic acid, the effects of specific inhibitors of the electron transport chain components on mitochondrial reactive oxygen species (ROS) production and Ca(2+) mobilization in HEp-2 cells were investigated. It was revealed that the mitochondrial complex III inhibitor (antimycin A) amplifies ascorbate-induced Ca(2+) release from intracellular stores. The mitochondrial complex I inhibitor (rotenone) decreases Ca(2+) release from intracellular stores in HEp-2 cells caused by ascorbic acid and antimycin A. In the presence of rotenone, antimycin A stimulates ROS production by mitochondria. Ascorbate-induced Ca(2+) release in HEp-2 cells is shown to be unaffected by catalase. The results obtained suggest that Ca(2+) release in HEp-2 cells caused by ascorbic acid is associated with induced mitochondrial ROS production. The data obtained are in line with the concept of redox signaling that explains oxidant action by compartmentalization of ROS production and oxidant targets. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
|
