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
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 |
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