Calcium as a reliable marker for the quantitative assessment of endoplasmic reticulum stress in live cells

Calcium (Ca 2+ ) is an essential mineral of endoplasmic reticulum (ER) luminal biochemistry because of the Ca 2+ dependence of ER-resident chaperones charged with folding de novo proteins that transit this cellular compartment. ER Ca 2+ depletion reduces the ability of chaperones to properly fold the proteins entering the ER, thus leading to an accumulation of misfolded proteins and the onset of a state known as ER stress. However, not all conditions that cause ER stress do so in a manner dependent on ER Ca 2+ depletion. Agents such as tunicamycin inhibit the glycosylation of de novo polypeptides, a key step in the maturation process of newly synthesized proteins. Despite this established effect of tunicamycin, our understanding of how such conditions modulate ER Ca 2+ levels is still limited. In the present study, we report that a variety of ER stress–inducing agents that have not been known to directly alter ER Ca 2+ homeostasis can also cause a marked reduction in ER Ca 2+ levels. Consistent with these observations, protecting against ER stress using small chemical chaperones, such as 4-phenylbutyrate and tauroursodeoxycholic acid, also attenuated ER Ca 2+ depletion caused by these agents. We also describe a novel high-throughput and low-cost assay for the rapid quantification of ER stress using ER Ca 2+ levels as a surrogate marker. This report builds on our understanding of ER Ca 2+ levels in the context of ER stress and also provides the scientific community with a new, reliable tool to study this important cellular process in vitro .