内质网
钙
细胞生物学
细胞器
钙信号传导
生物
生物学中的钙
钙代谢
平衡
钙显像
诱导多能干细胞
神经退行性变
细胞
生物化学
病理
细胞内
内科学
医学
疾病
胚胎干细胞
基因
作者
Mark J. Henderson,Heather A. Baldwin,Christopher A. Werley,Stefano Boccardo,Leslie R. Whitaker,Xiaokang Yan,Graham T. Holt,Eric R. Schreiter,Loren L. Looger,Adam E. Cohen,Douglas S. Kim,Brandon K. Harvey
出处
期刊:PLOS ONE
[Public Library of Science]
日期:2015-10-09
卷期号:10 (10): e0139273-e0139273
被引量:67
标识
DOI:10.1371/journal.pone.0139273
摘要
Endoplasmic reticulum calcium homeostasis is critical for cellular functions and is disrupted in diverse pathologies including neurodegeneration and cardiovascular disease. Owing to the high concentration of calcium within the ER, studying this subcellular compartment requires tools that are optimized for these conditions. To develop a single-fluorophore genetically encoded calcium indicator for this organelle, we targeted a low affinity variant of GCaMP3 to the ER lumen (GCaMPer (10.19)). A set of viral vectors was constructed to express GCaMPer in human neuroblastoma cells, rat primary cortical neurons, and human induced pluripotent stem cell-derived cardiomyocytes. We observed dynamic changes in GCaMPer (10.19) fluorescence in response to pharmacologic manipulations of the ER calcium store. Additionally, periodic calcium efflux from the ER was observed during spontaneous beating of cardiomyocytes. GCaMPer (10.19) has utility in imaging ER calcium in living cells and providing insight into luminal calcium dynamics under physiologic and pathologic states.
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