P38 Kinase, SGK1 and NF-κB Dependent Up-Regulation of Na < sup > + < /sup > /Ca < sup > 2+ < /sup > Exchanger Expression and Activity Following TGFß1 Treatment of Megakaryocytes

dc.contributor.author Al-Maghout, Tamer
dc.contributor.author Pelzl, Lisann
dc.contributor.author Sahu, Itishri
dc.contributor.author Sukkar, Basma
dc.contributor.author Hosseinzadeh, Zohreh
dc.contributor.author Gutti, Ravi
dc.contributor.author Laufer, Stefan
dc.contributor.author Voelkl, Jakob
dc.contributor.author Pieske, Burkert
dc.contributor.author Gawaz, Meinrad
dc.contributor.author Lang, Florian
dc.date.accessioned 2022-03-27T04:52:25Z
dc.date.available 2022-03-27T04:52:25Z
dc.date.issued 2017-10-01
dc.description.abstract 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.
dc.identifier.citation Cellular Physiology and Biochemistry. v.42(6)
dc.identifier.issn 10158987
dc.identifier.uri 10.1159/000479992
dc.identifier.uri https://www.karger.com/Article/FullText/479992
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/7378
dc.subject Calcium
dc.subject NCKX1
dc.subject NCKX2
dc.subject NCKX5
dc.subject NCX1
dc.subject NF-κB
dc.subject p38 kinase
dc.subject SGK1
dc.title P38 Kinase, SGK1 and NF-κB Dependent Up-Regulation of Na < sup > + < /sup > /Ca < sup > 2+ < /sup > Exchanger Expression and Activity Following TGFß1 Treatment of Megakaryocytes
dc.type Journal. Article
dspace.entity.type
Files
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.71 KB
Format:
Plain Text
Description: