P38 Kinase, SGK1 and NF-κB Dependent Up-Regulation of Na+/Ca2+ Exchanger Expression and Activity Following TGFß1 Treatment of Megakaryocytes

Background: TGFβ1, a decisive regulator of megakaryocyte maturation and platelet formation, has previously been shown to up-regulate both, store operated Ca 2+ entry (SOCE) and Ca 2+ extrusion by Na + /Ca 2+ exchange. The growth factor thus augments the increase of cytosolic Ca 2+ activity ([Ca 2+ ]...

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Veröffentlicht in:Cellular physiology and biochemistry 2017, Vol.42 (6), p.2169-2181
Hauptverfasser: Al-Maghout, Tamer, Pelzl, Lisann, Sahu, Itishri, Sukkar, Basma, Hosseinzadeh, Zohreh, Gutti, Ravi, Laufer, Stefan, Voelkl, Jakob, Pieske, Burkert, Gawaz, Meinrad, Lang, Florian
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Sprache:eng
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Zusammenfassung:Background: TGFβ1, a decisive regulator of megakaryocyte maturation and platelet formation, has previously been shown to up-regulate both, store operated Ca 2+ entry (SOCE) and Ca 2+ extrusion by Na + /Ca 2+ exchange. The growth factor thus augments the increase of cytosolic Ca 2+ activity ([Ca 2+ ] i ) following release of Ca 2+ from intracellular stores and accelerates the subsequent decline of [Ca 2+ ] 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 + /Ca 2+ exchanger isoforms involved and the signalling regulating the Na + /Ca 2+ exchangers remained, however elusive. The present study explored, whether TGFβ1 influences the expression and function of K + insensitive (NCX) and K + sensitive (NCKX) Na + /Ca 2+ 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, [Ca 2+ ] i was determined by Fura-2 fluorescence, and Na + /Ca 2+ exchanger activity was estimated from the increase of [Ca 2+ ] i following switch from an extracellular solution with 130 or 90 mM Na + and 0 mM Ca 2+ to an extracellular solution with 0 Na + and 2 mM Ca 2+ . 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 + /Ca 2+ exchanger activity, an effect requiring p38 kinase, SGK1 and NFκB.
ISSN:1015-8987
1421-9778
DOI:10.1159/000479992