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转化生长因子β1处理后巨核细胞中钠/钙交换体的上调

Up-Regulation of Na+/Ca2+ Exchange in Megakaryocytes Following TGFβ1 Treatment.

作者信息

Almilaji Ahmad, Yan Jing, Hosseinzadeh Zohreh, Schmid Evi, Gawaz Meinrad, Lang Florian

机构信息

Department of Cardiology, Vascular Medicine and Physiology, Eberhard-Karls-University of Tuebingen, Tuebingen, Germany.

出版信息

Cell Physiol Biochem. 2016;39(2):693-9. doi: 10.1159/000445660. Epub 2016 Jul 21.

Abstract

BACKGROUND

Blood platelets are activated by increase of cytosolic Ca2+ activity ([Ca2+]i). Ca2+ entry is accomplished in part by store operated Ca2+ entry (SOCE) involving Ca2+ release activated Ca2+-channel (CRAC) moiety Orai1 and its regulator STIM1, which are stimulated by depletion of intracellular Ca2+ stores. An increase of [Ca2+]i is terminated by Na+/Ca2+-exchange. The expression of both, Orai1 and STIM1 in megakaryocytes is up-regulated by tumor growth factor TGFβ1, a powerful regulator of megakaryocyte differentiation. The present study explored whether TGFβ1 similarly modifies megakaryocyte Na+/Ca2+-exchanger activity.

METHODS

[Ca2+]i was determined utlizing Fura-2 fluorescence, SOCE from increase of [Ca2+]i, following readdition of extracellular Ca2+ after store depletion, and Na+/Ca2+-exchanger activity from increase of [Ca2+]i and whole cell currents following removal of extracellular Na+.

RESULTS

TGFβ1 treatment not only augments the increase of [Ca2+]i following store depletion and SOCE, but significantly up-regulates Na+/Ca2+-exchanger activity as apparent from [Ca2+]i measurements and whole cell currents.

CONCLUSIONS

TGFβ1 is a powerful stimulator of both, SOCE and Na+/Ca2+-exchanger activity in megakaryocytes.

摘要

背景

血小板通过胞质Ca2+活性([Ca2+]i)升高而被激活。Ca2+内流部分通过储存操纵性Ca2+内流(SOCE)来完成,该过程涉及Ca2+释放激活的Ca2+通道(CRAC)成分Orai1及其调节因子STIM1,它们受到细胞内Ca2+储存耗竭的刺激。[Ca2+]i的升高通过Na+/Ca2+交换而终止。巨核细胞中Orai1和STIM1的表达均由肿瘤生长因子TGFβ1上调,TGFβ1是巨核细胞分化的有力调节因子。本研究探讨了TGFβ1是否同样改变巨核细胞的Na+/Ca2+交换活性。

方法

利用Fura-2荧光测定[Ca2+]i,通过储存耗竭后重新添加细胞外Ca2+后[Ca2+]i的升高来测定SOCE,以及通过去除细胞外Na+后[Ca2+]i的升高和全细胞电流来测定Na+/Ca2+交换活性。

结果

TGFβ1处理不仅增强了储存耗竭和SOCE后[Ca2+]i的升高,而且从[Ca2+]i测量值和全细胞电流来看,显著上调了Na+/Ca2+交换活性。

结论

TGFβ1是巨核细胞中SOCE和Na+/Ca2+交换活性的有力刺激因子。

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