Stanniocalcin 2 (STC2) is a fish protein that controls body Ca and phosphate metabolism. STC2 has also been described in mammals, and as platelet function highly depends on both extracellular and intracellular Ca, we have explored its expression and function in these cells. STC2 mice exhibit shorter tail bleeding time than WT mice. Platelets from STC2-deficient mice showed enhanced aggregation, as well as enhanced Ca mobilization in response to the physiological agonist thrombin (Thr) and the diacylglycerol analog, OAG, a selective activator of the non-capacitative Ca entry channels. Interestingly, platelets from STC2 mice exhibit attenuated interaction between STIM1 and Orai1 in response to Thr, thus suggesting that STC2 is required for Thr-evoked STIM1-Orai1 interaction and the subsequent store-operated Ca entry (SOCE). We have further assessed possible changes in the expression of the most relevant channels involved in non-capacitative Ca entry in platelets. Then, protein expression of Orai3, TRPC3 and TRPC6 were evaluated by Western blotting, and the results revealed that while the expression of Orai3 was enhanced in the STC2-deficient mice, others like TRPC3 and TRPC6 remains almost unaltered. Summarizing, our results provide for the first time evidence for a role of STC2 in platelet physiology through the regulation of agonist-induced Ca entry, which might be mediated by the regulation of Orai3 channel expression.
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http://dx.doi.org/10.3389/fphys.2018.00266 | DOI Listing |
Int J Mol Sci
November 2022
Department of Physiology (Cellular Physiology Research Group), Institute of Molecular Pathology Biomarkers (IMPB), University of Extremadura, 10003 Caceres, Spain.
Orai1, the first identified member of the Orai protein family, is ubiquitously expressed in the animal kingdom. Orai1 was initially characterized as the channel responsible for the store-operated calcium entry (SOCE), a major mechanism that allows cytosolic calcium concentration increments upon receptor-mediated IP generation, which results in intracellular Ca store depletion. Furthermore, current evidence supports that abnormal Orai1 expression or function underlies several disorders.
View Article and Find Full Text PDFFront Physiol
March 2018
Department of Physiology (PHYCELL) of the Veterinary Faculty, University of Extremadura, Cáceres, Spain.
Stanniocalcin 2 (STC2) is a fish protein that controls body Ca and phosphate metabolism. STC2 has also been described in mammals, and as platelet function highly depends on both extracellular and intracellular Ca, we have explored its expression and function in these cells. STC2 mice exhibit shorter tail bleeding time than WT mice.
View Article and Find Full Text PDFWorld J Nephrol
January 2016
Alessandra Mangolini, Lucia de Stephanis, Gianluca Aguiari, Department of Biomedical and Surgical Specialty Sciences, Section of Biochemistry, Molecular Biology and Medical Genetics, University of Ferrara, 44121 Ferrara, Italy.
Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited monogenic kidney disease. Characterized by the development and growth of cysts that cause progressive kidney enlargement, it ultimately leads to end-stage renal disease. Approximately 85% of ADPKD cases are caused by mutations in the PKD1 gene, while mutations in the PKD2 gene account for the remaining 15% of cases.
View Article and Find Full Text PDFBiochim Biophys Acta
October 2015
Department of Physiology, Cell Physiology Research Group, University of Extremadura, 10003 Cáceres, Spain. Electronic address:
Non-capacitative calcium entry (NCCE) contributes to cell activation in response to the occupation of G protein-coupled membrane receptors. Thrombin administration to platelets evokes the synthesis of diacylglycerol downstream of PAR receptor activation. Diacylglycerol evokes NCCE through activating TRPC3 and TRPC6 in human platelets.
View Article and Find Full Text PDFHistochem Cell Biol
October 2013
Department of Anatomy (Cell Biology), Iwate Medical University, 2-1-1 Nishitokuda, Yahaba, Iwate, 028-3694, Japan.
Protease-activated receptors (PARs) represent a novel class of seven transmembrane domain G-protein coupled receptors, which are activated by proteolytic cleavage. PARs are present in a variety of cells and have been prominently implicated in the regulation of a number of vital functions. Here, lacrimal gland acinar cell responses to PAR activation were examined, with special reference to intracellular Ca(2+) concentration ([Ca(2+)]i) dynamics.
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