Ziomek Gabriela, van Breemen Cornelis, Esfandiarei Mitra
Department of Anaesthesiology, Pharmacology, and Therapeutics, University of British Columbia.
Department of Anaesthesiology, Pharmacology, and Therapeutics, University of British Columbia; Department of Biomedical Sciences, Midwestern University;
J Vis Exp. 2016 Jun 20(112):53912. doi: 10.3791/53912.
Maintenance of steady-state calcium (Ca(2+)) levels in the sarcoplasmic reticulum (SR) of vascular smooth muscle cells (VSMCs) is vital to their overall health. A significant portion of intracellular Ca(2+) content is found within the SR stores in VSMCs. As the only intracellular organelle with a close association to the surrounding extracellular space through plasma membrane-SR junctions, the SR can be considered to constitute the first line of response to any irregularity in Ca(2+) transients, or stress experienced by the cell. Among its many functions, one of the most important is its role in the transmission of Ca(2+)-regulated signals throughout the cell to induce further cell-wide reactions downstream. The more common use of cytoplasmic Ca(2+) indicators in this regard is overall insufficient for research into the highly dynamic changes to the intraluminal SR Ca(2+) store that have yet to be fully characterized. Here, we provide a detailed protocol for the direct and clear measurement of luminal SR Ca(2+). This tool is useful for investigation into the nuanced changes in SR Ca(2+) that have significant subsequent effects on the normal function and health of the cell. Fluctuations in SR Ca(2+) content specifically can provide us with a significant amount of information pertaining to cellular responses to disease or stress conditions experienced by the cell. In this method, a modified version of a SR-targeted Ca(2+) indicator, D1SR, is used to detect Ca(2+) fluctuations in response to the introduction of agents to cultured rat aortic smooth muscle cells (SMCs). Following incubation with the D1SR indicator, confocal fluorescence microscopy and fluorescence resonance energy transfer (FRET)-based imaging are used to directly observe changes to intraluminal SR Ca(2+) levels under control conditions and with the addition of agonist agents that function to induce intracellular Ca(2+) movement.
维持血管平滑肌细胞(VSMCs)肌浆网(SR)中稳态钙(Ca(2+))水平对其整体健康至关重要。VSMCs细胞内Ca(2+)含量的很大一部分存在于SR储存库中。作为唯一通过质膜-SR连接与周围细胞外空间紧密相连的细胞内细胞器,SR可被视为对Ca(2+)瞬变或细胞所经历的应激的任何异常情况做出反应的第一道防线。在其众多功能中,最重要的功能之一是它在将Ca(2+)调节信号传递到整个细胞以诱导下游进一步的全细胞反应中所起的作用。在这方面,更常用的细胞质Ca(2+)指示剂总体上不足以研究管腔内SR Ca(2+)储存库尚未完全表征的高度动态变化。在这里,我们提供了一种直接且清晰地测量管腔内SR Ca(2+)的详细方案。该工具对于研究SR Ca(2+)的细微变化很有用,这些变化对细胞的正常功能和健康有重大的后续影响。SR Ca(2+)含量的波动具体可以为我们提供大量与细胞对疾病或细胞所经历的应激条件的反应相关的信息。在该方法中,一种经过改良的靶向SR的Ca(2+)指示剂D1SR用于检测向培养的大鼠主动脉平滑肌细胞(SMCs)中引入试剂后Ca(2+)的波动。在用D1SR指示剂孵育后,共聚焦荧光显微镜和基于荧光共振能量转移(FRET)的成像用于直接观察在对照条件下以及添加用于诱导细胞内Ca(2+)移动的激动剂时管腔内SR Ca(2+)水平的变化。