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Calcium, mitochondria and apoptosis studied by fluorescence measurements.

机译:通过荧光测量研究钙,线粒体和细胞凋亡。

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Among the many unsolved problems of calcium signalling, the role of calcium elevations in apoptotic and necrotic cell death has been a focus of research in recent years. Evidence has been presented that calcium oscillations can effectively trigger apoptosis under certain conditions and that dysregulation of calcium signalling is a common cause of cell death. These effects are regularly mediated through calcium signal propagation to the mitochondria and the ensuing mitochondrial membrane permeabilization and release of pro-apoptotic factors from mitochondria to the cytoplasm. The progress in this area depended on the development of (1) fluorescent/luminescent probes, including fluorescent proteins that can be genetically targeted to different intracellular locations and (2) the digital imaging technology, fluorescence-activated cell sorting and fluorescent high throughput approaches, which allowed dynamic measurements of both [Ca2+] in the intracellular compartments of interest and the downstream processes. Fluorescence single cell imaging has been the only possible approach to resolve the cell-to-cell heterogeneity and the complex subcellular spatiotemporal organization of the cytoplasmic and mitochondrial calcium signals and downstream events. We outline here fluorometric and fluorescence imaging protocols that we set up for the study of calcium in the context of apoptosis.
机译:在许多尚未解决的钙信号传递问题中,近年来钙升高在凋亡和坏死细胞死亡中的作用一直是研究的重点。已有证据表明,钙振荡可在某些条件下有效触发细胞凋亡,而钙信号传导失调是细胞死亡的常见原因。这些作用通常通过钙信号传播到线粒体和随后的线粒体膜通透性以及促凋亡因子从线粒体到细胞质的释放而介导。该领域的进展取决于(1)荧光/发光探针的开发,包括可以遗传靶向不同细胞内位置的荧光蛋白,以及(2)数字成像技术,荧光激活细胞分选和荧光高通量方法,可以动态测量目标细胞内区室和下游过程中的[Ca2 +]。荧光单细胞成像已经成为解决细胞间异质性以及胞质和线粒体钙信号和下游事件的复​​杂亚细胞时空组织的唯一可能方法。我们在这里概述了荧光测定和荧光成像方案,这些方案是为了在细胞凋亡的背景下研究钙而建立的。

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