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通过正常和病理性半通道摄取 Ca 的定量测定。

A Quantitative Assay for Ca Uptake through Normal and Pathological Hemichannels.

机构信息

CNR Institute of Biochemistry and Cell Biology, Monterotondo, 00015 Rome, Italy.

Shanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai 201210, China.

出版信息

Int J Mol Sci. 2022 Jun 30;23(13):7337. doi: 10.3390/ijms23137337.

Abstract

Connexin (Cx) hemichannels (HCs) are large pore hexameric structures that allow the exchange of ions, metabolites and a variety of other molecules between the cell cytoplasm and extracellular milieu. HC inhibitors are attracting growing interest as drug candidates because deregulated fluxes through HCs have been implicated in a plethora of genetic conditions and other diseases. HC activity has been mainly investigated by electrophysiological methods and/or using HC-permeable dye uptake measurements. Here, we present an all-optical assay based on fluorometric measurements of ionized calcium (Ca) uptake with a Ca-selective genetically encoded indicator (GCaMP6s) that permits the optical tracking of cytosolic Ca concentration ([Ca]) changes with high sensitivity. We exemplify use of the assay in stable pools of HaCaT cells overexpressing human Cx26, Cx46, or the pathological mutant Cx26G45E, under control of a tetracycline (Tet) responsive element (TRE) promoter (Tet-on). We demonstrate the usefulness of the assay for the characterization of new monoclonal antibodies (mAbs) targeting the extracellular domain of the HCs. Although we developed the assay on a spinning disk confocal fluorescence microscope, the same methodology can be extended seamlessly to high-throughput high-content platforms to screen other kinds of inhibitors and/or to probe HCs expressed in primary cells and microtissues.

摘要

间隙连接 (Cx) 半通道 (HC) 是一种大型六聚体结构,允许细胞细胞质和细胞外环境之间交换离子、代谢物和各种其他分子。由于 HC 中失调的通量与许多遗传条件和其他疾病有关,因此 HC 抑制剂作为候选药物引起了越来越多的关注。HC 活性主要通过电生理学方法和/或使用 HC 通透染料摄取测量来研究。在这里,我们提出了一种基于荧光测量的全光学测定法,用于测量带有人钙选择基因编码指示剂 (GCaMP6s) 的离子化钙 (Ca) 摄取,该测定法具有高灵敏度,可用于光学跟踪细胞质 Ca 浓度 ([Ca]) 的变化。我们举例说明了该测定法在稳定的 HaCaT 细胞池中的用途,这些细胞过表达人 Cx26、Cx46 或病理突变体 Cx26G45E,受四环素 (Tet) 反应元件 (TRE) 启动子 (Tet-on) 的控制。我们证明了该测定法对于表征针对 HC 细胞外结构域的新型单克隆抗体 (mAb) 的有用性。尽管我们在旋转盘共聚焦荧光显微镜上开发了该测定法,但相同的方法可以无缝扩展到高通量高内涵平台,以筛选其他类型的抑制剂和/或探测原代细胞和微组织中表达的 HC。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf87/9266989/1784620dd79e/ijms-23-07337-g001.jpg

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