首页> 外文期刊>Journal of Bioenergetics and Biomembranes >The interplay between plasma membrane and endoplasmic reticulum Ca~(2+)ATPases in agonist-induced temporal Ca~(2+) dynamics
【24h】

The interplay between plasma membrane and endoplasmic reticulum Ca~(2+)ATPases in agonist-induced temporal Ca~(2+) dynamics

机译:激动剂诱导的瞬时Ca〜(2+)动力学中质膜与内质网Ca〜(2+)ATPase的相互作用

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

A change in the intracellular free Ca~(2+) concentration([Ca~(2+)]i) functions as a transmitter for signal transduction and shows a broad temporal pattern. Even genetically homogeneous cell types show different Ca~(2+) response patterns under permanent agonist stimulation. In Ca~(2+) signaling, the dynamics of the Ca~(2+) release from the Ca~(2+) channels during continuous agonist stimulation and the simultaneous effect of the pumps are unclear. In this study, the dynamic interaction of the Ca~(2+) ATPases in the plasma membrane (PMCA) and the endoplasmic reticulum membrane (SERCA) during continuous ACh stimulation is monitored using Fluo-3 and Fura-2 loaded HEK 293 cells. We characterize Ca~(2+) release patterns at the sub-maximal and maximal stimulation doses in the absence of extracellular Ca~(2+). We analyze the responses regarding their types, oscillation frequency and response times. La~(3+) (PMCA blocker) do not change the frequency and time courses in sub-maximal ACh treatment, while with the maximal stimulation oscillation frequency increase as oscillations superimpose on robust release, and response time of [Ca~(2+)]i is elongated. A similar effect of La~(3+) is observed in quantal Ca~(2+) release phenomenon. In the presence of CPA, a SERCA blocker, oscillations are completely abolished, but response time does not change.We also observe that during continuous receptor stimulation, Ca~(2+) release do not cease. These data may suggest that Ca~(2+) release continues during agonist stimulation, but SERCA and PMCA form a new steady state and return [Ca~(2+)]i to its physiological concentration.
机译:细胞内游离Ca〜(2+)浓度([Ca〜(2 +)] i)的变化充当信号转导的发送器,并显示出宽泛的时间模式。甚至遗传上均一的细胞类型在永久性激动剂刺激下也显示出不同的Ca〜(2+)反应模式。在Ca〜(2+)信号传导中,在连续激动剂刺激期间Ca〜(2+)从Ca〜(2+)通道释放的动力学以及泵的同时作用尚不清楚。在这项研究中,使用Fluo-3和Fura-2负载的HEK 293细胞监测连续ACh刺激期间质膜(PMCA)和内质网膜(SERCA)中Ca〜(2+)ATPase的动态相互作用。我们在没有细胞外Ca〜(2+)的情况下,以次最大和最大刺激剂量表征Ca〜(2+)的释放模式。我们分析有关它们的类型,振荡频率和响应时间的响应。 La〜(3+)(PMCA阻滞剂)在次最大ACh治疗中不会改变频率和时间进程,而随着最大刺激振荡频率的增加,因为振荡叠加在稳健释放上,响应时间为[Ca〜(2+ )] i拉长了。在定量的Ca〜(2+)释放现象中观察到了La〜(3+)的类似作用。在存在SERCA阻断剂CPA的情况下,振荡被完全消除,但响应时间没有改变。我们还观察到在连续的受体刺激过程中,Ca〜(2+)释放不会停止。这些数据可能表明在激动剂刺激过程中Ca〜(2+)释放继续,但是SERCA和PMCA形成新的稳定状态并使[Ca〜(2 +)] i返回其生理浓度。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号