SERCA Modulators Reveal Distinct Signaling and Functional Roles of T Lymphocyte Ca(2+) Stores

SERCA调节剂揭示T淋巴细胞Ca(2+)储存的独特信号传导和功能作用

阅读:1

Abstract

The allosteric SERCA (Sarcoplasmic/Endoplasmic Reticulum Ca(2+)-ATPase) activator CDN1163 has been recently added to the group of pharmacological tools for probing SERCA function. We chose to investigate the effects of the compound on T lymphocyte Ca(2+) stores, using the well-described Jurkat T lymphocyte as a reliable cell system for Ca(2+) signaling pathways. Our study identified the lowest concentrations of the SERCA inhibitors thapsigargin (TG) and 2,5-di-(tert butyl)-1,4-benzohydroquinone (tBHQ) capable of releasing Ca(2+), permitting the differentiation of the TG-sensitive SERCA 2b Ca(2+) store from the tBHQ-sensitive SERCA 3 Ca(2+) store. We proceeded to test the effects of CDN1163 on Ca(2+) stores, examining specific actions on the SERCA 2b and SERCA 3 Ca(2+) pools using our low-dose SERCA blocker regimen. In contrast to previous work, we find CDN1163 exerts complex time-sensitive and SERCA isoform-specific actions on Ca(2+) stores. Surprisingly, short-term exposure (0-30 min) to CDN1163 perturbs T cell Ca(2+) stores by suppressing Ca(2+) uptake with diminished Ca(2+) release from the SERCA 2b-controlled store. Concomitantly, we find evidence for a SERCA-activating effect of CDN1163 on the SERCA-3 regulated store, given the observation of increased Ca(2+) release inducible by low-dose tBHQ. Intriguingly, longer-term (>12 h) CDN1163 exposure reversed this pattern, with increased Ca(2+) release from SERCA 2b-regulated pools yet decreased Ca(2+) release responses from the tBHQ-sensitive SERCA 3 pool. Indeed, this remodeling of SERCA 2b Ca(2+) stores with longer-term CDN1163 exposure also translated into the compound's ability to protect Jurkat T lymphocytes from TG but not tBHQ-induced growth suppression.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。