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同步测量胰腺β细胞中线粒体和内质网游离钙的变化。

Simultaneous Measurement of Changes in Mitochondrial and Endoplasmic Reticulum Free Calcium in Pancreatic Beta Cells.

机构信息

Department of Pharmacology, University of Michigan Medical School, Ann Arbor, MI 48105, USA.

Department of Internal Medicine, Division of Metabolism, Endocrinology & Diabetes, University of Michigan Medical School, Ann Arbor, MI 48105, USA.

出版信息

Biosensors (Basel). 2023 Mar 14;13(3):382. doi: 10.3390/bios13030382.

Abstract

The free calcium (Ca) levels in pancreatic beta cell organelles have been the subject of many recent investigations. Under pathophysiological conditions, disturbances in these pools have been linked to altered intracellular communication and cellular dysfunction. To facilitate studies of subcellular Ca signaling in beta cells and, particularly, signaling between the endoplasmic reticulum (ER) and mitochondria, we designed a novel dual Ca sensor which we termed DS-1. DS-1 encodes two stoichiometrically fluorescent proteins within a single plasmid, G-CEPIA-er, targeted to the ER and R-CEPIA3-mt, targeted to mitochondria. Our goal was to simultaneously measure the ER and mitochondrial Ca in cells in real time. The of G-CEPIA-er and R-CEPIA3-mt for Ca are 672 and 3.7 μM, respectively. Confocal imaging of insulin-secreting INS-1 832/13 expressing DS-1 confirmed that the green and red fluorophores correctly colocalized with organelle-specific fluorescent markers as predicted. Further, we tested whether DS-1 exhibited the functional properties expected by challenging an INS-1 cell to glucose concentrations or drugs having well-documented effects on the ER and mitochondrial Ca handling. The data obtained were consistent with those seen using other single organelle targeted probes. These results taken together suggest that DS-1 is a promising new approach for investigating Ca signaling within multiple organelles of the cell.

摘要

胰腺β细胞细胞器中的游离钙(Ca)水平一直是许多近期研究的主题。在病理生理条件下,这些池中的紊乱与细胞内通讯和细胞功能障碍的改变有关。为了促进β细胞亚细胞 Ca 信号转导的研究,特别是内质网(ER)和线粒体之间的信号转导,我们设计了一种新型的双 Ca 传感器,我们称之为 DS-1。DS-1 在单个质粒 G-CEPIA-er 中编码两个化学计量荧光蛋白,靶向 ER 和 R-CEPIA3-mt,靶向线粒体。我们的目标是实时同时测量细胞中的 ER 和线粒体 Ca。G-CEPIA-er 和 R-CEPIA3-mt 的 Ca 分别为 672 和 3.7 μM。用表达 DS-1 的胰岛素分泌 INS-1 832/13 进行共聚焦成像证实,绿色和红色荧光团与细胞器特异性荧光标记物如预测的那样正确共定位。此外,我们测试了 DS-1 是否表现出预期的功能特性,即用具有明确记载的 ER 和线粒体 Ca 处理作用的药物或葡萄糖浓度挑战 INS-1 细胞。获得的数据与使用其他单细胞器靶向探针观察到的数据一致。这些结果表明,DS-1 是研究细胞内多个细胞器 Ca 信号转导的一种很有前途的新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7769/10046164/fb770ab82c38/biosensors-13-00382-g001.jpg

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