Endoplasmic-Reticulum Calcium Depletion and Disease

Publication: ncbi.nlm.nih.gov | Publication Date: January 7, 2016

Authors: Fumihiko Urano

Abstract

The endoplasmic reticulum (ER) as an intracellular Ca2+ store not only sets up cytosolic Ca2+ signals, but, among other functions, also assembles and folds newly synthesized proteins. Alterations in ER homeostasis, including severe Ca2+ depletion, are an upstream event in the pathophysiology of many diseases. On the one hand, insufficient release of activator Ca2+ may no longer sustain essential cell functions. On the other hand, loss of luminal Ca2+ causes ER stress and activates an unfolded protein response, which, depending on the duration and severity of the stress, can reestablish normal ER function or lead to cell death. We will review these various diseases by mainly focusing on the mechanisms that cause ER Ca2+ depletion.

Mekahli, D., Bultynck, G., Parys, J. B., De Smedt, H., & Missiaen, L. (2011). Endoplasmic-reticulum calcium depletion and disease. Cold Spring Harbor perspectives in biology, 3(6), a004317. Retrieved February 4, 2024, from https://doi.org/10.1101/cshperspect.a004317.