SERCaMP: a carboxy-terminal protein modification that enables monitoring of ER calcium homeostasis

被引:47
作者
Henderson, Mark J. [1 ]
Wires, Emily S. [1 ]
Trychta, Kathleen A. [1 ]
Richie, Christopher T. [1 ]
Harvey, Brandon K. [1 ]
机构
[1] NIDA, Intramural Res Program, Baltimore, MD 21224 USA
关键词
ENDOPLASMIC-RETICULUM STRESS; SECRETORY PATHWAY; CA2+ ATPASE; IN-VITRO; INHIBITOR; CYCLO-OXYGENASE-2; MUTATIONS; REGULATOR; CELECOXIB; TOXICITY;
D O I
10.1091/mbc.E14-06-1141
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Endoplasmic reticulum (ER) calcium homeostasis is disrupted in diverse pathologies, including neurodegeneration, cardiovascular diseases, and diabetes. Temporally defining calcium dysregulation during disease progression, however, has been challenging. Here we describe secreted ER calcium-monitoring proteins (SERCaMPs), which allow for longitudinal monitoring of ER calcium homeostasis. We identified a carboxy-terminal modification that is sufficient to confer release of a protein specifically in response to ER calcium depletion. A Gaussia luciferase (GLuc)-based SERCaMP provides a simple and sensitive method to monitor ER calcium homeostasis in vitro or in vivo by analyzing culture medium or blood. GLuc-SERCaMPs revealed ER calcium depletion in rat primary neurons exposed to various ER stressors. In vivo, ER calcium disruption in rat liver was monitored over several days by repeated sampling of blood. Our results suggest that SERCaMPs will have broad applications for the long-term monitoring of ER calcium homeostasis and the development of therapeutic approaches to counteract ER calcium dysregulation.
引用
收藏
页码:2828 / 2839
页数:12
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