Critical contribution of Na+‐Ca2+ exchanger to the Ca2+‐mediated vasodilation activated in endothelial cells of resistance arteries. Issue 4 (5th January 2018)
- Record Type:
- Journal Article
- Title:
- Critical contribution of Na+‐Ca2+ exchanger to the Ca2+‐mediated vasodilation activated in endothelial cells of resistance arteries. Issue 4 (5th January 2018)
- Main Title:
- Critical contribution of Na+‐Ca2+ exchanger to the Ca2+‐mediated vasodilation activated in endothelial cells of resistance arteries
- Authors:
- Lillo, Mauricio A.
Gaete, Pablo S.
Puebla, Mariela
Ardiles, Nicolás M.
Poblete, Inés
Becerra, Alvaro
Simon, Felipe
Figueroa, Xavier F. - Abstract:
- Abstract : Na + ‐Ca 2+ exchanger (NCX) contributes to control the intracellular free Ca 2+ concentration ([Ca 2 +]i ), but the functional activation of NCX reverse mode (NCXrm) in endothelial cells is controversial. We evaluated the participation of NCXrm‐mediated Ca 2+ uptake in the endothelium‐dependent vasodilation of rat isolated mesenteric arterial beds. In phenylephrine‐contracted mesenteries, the acetylcholine (ACh)‐induced vasodilation was abolished by treatment with the NCXrm blockers SEA0400, KB‐R7943, or SN‐6. Consistent with that, the ACh‐induced hyperpolarization observed in primary cultures of mesenteric endothelial cells and in smooth muscle of isolated mesenteric resistance arteries was attenuated by KB‐R7943 and SEA0400, respectively. In addition, both blockers abolished the NO production activated by ACh in intact mesenteric arteries. In contrast, the inhibition of NCXrm did not affect the vasodilator responses induced by the Ca 2+ ionophore, ionomycin, and the NO donor, S‐nitroso‐ N ‐acetylpenicillamine. Furthermore, SEA0400, KB‐R7943, and a small interference RNA directed against NCX1 blunted the increase in [Ca 2+ ]i induced by ACh or ATP in cultured endothelial cells. The analysis by proximity ligation assay showed that the NO‐synthesizing enzyme, eNOS, and NCX1 were associated in endothelial cell caveolae of intact mesenteric resistance arteries. These results indicate that the activation of NCXrm has a central role in Ca 2+ ‐mediated vasodilationAbstract : Na + ‐Ca 2+ exchanger (NCX) contributes to control the intracellular free Ca 2+ concentration ([Ca 2 +]i ), but the functional activation of NCX reverse mode (NCXrm) in endothelial cells is controversial. We evaluated the participation of NCXrm‐mediated Ca 2+ uptake in the endothelium‐dependent vasodilation of rat isolated mesenteric arterial beds. In phenylephrine‐contracted mesenteries, the acetylcholine (ACh)‐induced vasodilation was abolished by treatment with the NCXrm blockers SEA0400, KB‐R7943, or SN‐6. Consistent with that, the ACh‐induced hyperpolarization observed in primary cultures of mesenteric endothelial cells and in smooth muscle of isolated mesenteric resistance arteries was attenuated by KB‐R7943 and SEA0400, respectively. In addition, both blockers abolished the NO production activated by ACh in intact mesenteric arteries. In contrast, the inhibition of NCXrm did not affect the vasodilator responses induced by the Ca 2+ ionophore, ionomycin, and the NO donor, S‐nitroso‐ N ‐acetylpenicillamine. Furthermore, SEA0400, KB‐R7943, and a small interference RNA directed against NCX1 blunted the increase in [Ca 2+ ]i induced by ACh or ATP in cultured endothelial cells. The analysis by proximity ligation assay showed that the NO‐synthesizing enzyme, eNOS, and NCX1 were associated in endothelial cell caveolae of intact mesenteric resistance arteries. These results indicate that the activation of NCXrm has a central role in Ca 2+ ‐mediated vasodilation initiated by ACh in endothelial cells of resistance arteries.— Lillo, M. A., Gaete, P. S., Puebla, M., Ardiles, N. M., Poblete, I., Becerra, A., Simon, F., Figueroa, X. F. Critical contribution of Na+‐Ca2+ exchanger to the Ca2+‐mediated vasodilation activated in endothelial cells of resistance arteries. FASEB J. 32, 2137–2147 (2018). www.fasebj.org … (more)
- Is Part Of:
- FASEB journal. Volume 32:Issue 4(2018)
- Journal:
- FASEB journal
- Issue:
- Volume 32:Issue 4(2018)
- Issue Display:
- Volume 32, Issue 4 (2018)
- Year:
- 2018
- Volume:
- 32
- Issue:
- 4
- Issue Sort Value:
- 2018-0032-0004-0000
- Page Start:
- 2137
- Page End:
- 2147
- Publication Date:
- 2018-01-05
- Subjects:
- NO production -- endothelium‐dependent vasodilation -- endothelium‐derived hyperpolarization -- Ca2+ signaling -- endothelial NO synthase
Biology -- Periodicals
Biology, Experimental -- Periodicals
570 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1096/fj.201700365RR ↗
- Languages:
- English
- ISSNs:
- 0892-6638
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 13220.xml