| Autor: |
Vasauskas AA; Departments of Biochemistry and Molecular Biology and Center for Lung Biology, University of South Alabama, Mobile, Alabama, USA., Chen H; Department of Anesthesiology and Perioperative Medicine, Georgia Regents University, Augusta, Georgia, USA., Wu S; Department of Anesthesiology and Perioperative Medicine, Georgia Regents University, Augusta, Georgia, USA., Cioffi DL; Departments of Biochemistry and Molecular Biology and Center for Lung Biology, University of South Alabama, Mobile, Alabama, USA. |
| Jazyk: |
angličtina |
| Zdroj: |
Pulmonary circulation [Pulm Circ] 2014 Mar; Vol. 4 (1), pp. 116-27. |
| DOI: |
10.1086/675641 |
| Abstrakt: |
Disruption of the endothelium leads to increased permeability, allowing extravasation of macromolecules and other solutes from blood vessels. Calcium entry through a calcium-selective, store-operated calcium (SOC) channel, I soc, contributes to barrier disruption. An understanding of the mechanisms surrounding the regulation of I soc is far from complete. We show that the calcium/calmodulin-activated phosphatase calcineurin (CN) plays a role in regulation of SOC entry, possibly through the dephosphorylation of stromal interaction molecule 1 (STIM1). Phosphorylation has been implicated as a regulatory mechanism of activity for a number of canonical transient receptor potential (TRPC) and SOC channels, including I soc. Our results show that STIM1 phosphorylation increases in pulmonary artery endothelial cells (PAECs) upon activation of SOC entry. However, the phosphatases involved in STIM1 dephosphorylation are unknown. We found that a CN inhibitor (calcineurin inhibitory peptide [CIP]) increases the phosphorylation pattern of STIM1. Using a fura 2-acetoxymethyl ester approach to measure cytosolic calcium in PAECs, we found that CIP decreases SOC entry following thapsigargin treatment in PAECs. Luciferase assays indicate that thapsigargin induces activation of CN activity and confirm inhibition of CN activity by CIP in PAECs. Also, I soc is significantly attenuated in whole-cell patch-clamp studies of PAECs treated with CIP. Finally, PAECs pretreated with CIP exhibit decreased interendothelial cell gap formation in response to thapsigargin-induced SOC entry, as compared to control cells. Taken together, our data show that CN contributes to the phosphorylation status of STIM1, which is important in regulation of endothelial SOC entry and I soc activity. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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