P38 Kinase, SGK1 and NF-κB Dependent Up-Regulation of Na+/Ca2+ Exchanger Expression and Activity Following TGFß1 Treatment of Megakaryocytes
Open Access
- 15 August 2017
- journal article
- research article
- Published by S. Karger AG in Cellular Physiology and Biochemistry
- Vol. 42 (6) , 2169-2181
Abstract
Background: TGFβ1, a decisive regulator of megakaryocyte maturation and platelet formation, has previously been shown to up-regulate both, store operated Ca2+ entry (SOCE) and Ca2+ extrusion by Na+/Ca2+ exchange. The growth factor thus augments the increase of cytosolic Ca2+ activity ([Ca2+]i) following release of Ca2+ from intracellular stores and accelerates the subsequent decline of [Ca2+]i. The effect on SOCE is dependent on a signaling cascade including p38 kinase, serum & glucocorticoid inducible kinase SGK1, and nuclear factor NFκB. The specific Na+/Ca2+ exchanger isoforms involved and the signalling regulating the Na+/Ca2+ exchangers remained, however elusive. The present study explored, whether TGFβ1 influences the expression and function of K+ insensitive (NCX) and K+ sensitive (NCKX) Na+/Ca2+ exchangers, and aimed to shed light on the signalling involved. Methods: In human megakaryocytic cells (MEG01) RT-PCR was performed to quantify NCX/NCKX isoform transcript levels, [Ca2+]i was determined by Fura-2 fluorescence, and Na+/Ca2+ exchanger activity was estimated from the increase of [Ca2+]i following switch from an extracellular solution with 130 or 90 mM Na+ and 0 mM Ca2+ to an extracellular solution with 0 Na+ and 2 mM Ca2+. K+ concentration was 0 mM for analysis of NCX and 40 mM for analysis of NCKX. Results: TGFβ1 (60 ng/ml, 24 h) significantly increased the transcript levels of NCX1, NCKX1, NCKX2 and NCKX5. Moreover, TGFβ1 (60 ng/ml, 24 h) significantly increased the activity of both, NCX and NCKX. The effect of TGFβ1 on NCX and NCKX transcript levels and activity was significantly blunted by p38 kinase inhibitor Skepinone-L (1 µM), the effect on NCX and NCKX activity further by SGK1 inhibitor GSK-650394 (10 µM) and NFκB inhibitor Wogonin (100 µM). Conclusions: TGFβ1 markedly up-regulates transcription of NCX1, NCKX1, NCKX2, and NCKX5 and thus Na+/Ca2+ exchanger activity, an effect requiring p38 kinase, SGK1 and NFκB.Keywords
This publication has 53 references indexed in Scilit:
- Effect of TGFβ on calcium signaling in megakaryocytesBiochemical and Biophysical Research Communications, 2015
- Effect of TGFβ on Na+/K+ ATPase activity in megakaryocytesBiochemical and Biophysical Research Communications, 2014
- Sodium-calcium exchangers (NCX): molecular hallmarks underlying the tissue-specific and systemic functionsPflügers Archiv - European Journal of Physiology, 2013
- Role of Ion Transport in Control of Apoptotic Cell DeathComprehensive Physiology, 2012
- The relationship of the active and latent forms of TGF-β1 with marrow fibrosis in essential thrombocythemia and primary myelofibrosisMedical Oncology, 2011
- Calcium wave signaling in cancer cellsLife Sciences, 2010
- Calcium microdomains: Organization and functionCell Calcium, 2006
- Calcium entry mediated by SOCs and TRP channels: variations and enigmaBiochimica et Biophysica Acta (BBA) - Molecular Cell Research, 2004
- h-sgk serine-threonine protein kinase gene as transcriptional target of transforming growth factor β in human intestineGastroenterology, 1999
- Bradykinin-induced oscillations of cell membrane potential in cells expressing the Ha-ras oncogene.Journal of Biological Chemistry, 1991