A Highly Sensitive Assay for Monitoring the Secretory Pathway and ER Stress
Open Access
- 27 June 2007
- journal article
- research article
- Published by Public Library of Science (PLoS) in PLOS ONE
- Vol. 2 (6), e571
- https://doi.org/10.1371/journal.pone.0000571
Abstract
The secretory pathway is a critical index of the capacity of cells to incorporate proteins into cellular membranes and secrete proteins into the extracellular space. Importantly it is disrupted in response to stress to the endoplasmic reticulum that can be induced by a variety of factors, including expression of mutant proteins and physiologic stress. Activation of the ER stress response is critical in the etiology of a number of diseases, such as diabetes and neurodegeneration, as well as cancer. We have developed a highly sensitive assay to monitor processing of proteins through the secretory pathway and endoplasmic reticulum (ER) stress in real-time based on the naturally secreted Gaussia luciferase (Gluc). An expression cassette for Gluc was delivered to cells, and its secretion was monitored by measuring luciferase activity in the conditioned medium. Gluc secretion was decreased down to 90% when these cells were treated with drugs that interfere with the secretory pathway at different steps. Fusing Gluc to a fluorescent protein allowed quantitation and visualization of the secretory pathway in real-time. Expression of this reporter protein did not itself elicit an ER stress response in cells; however, Gluc proved very sensitive at sensing this type of stress, which is associated with a temporary decrease in processing of proteins through the secretory pathway. The Gluc secretion assay was over 20,000-fold more sensitive as compared to the secreted alkaline phosphatase (SEAP), a well established assay for monitoring of protein processing and ER stress in mammalian cells. The Gluc assay provides a fast, quantitative and sensitive technique to monitor the secretory pathway and ER stress and its compatibility with high throughput screening will allow discovery of drugs for treatment of conditions in which the ER stress is generally induced.Keywords
This publication has 32 references indexed in Scilit:
- Mutant torsinA interferes with protein processing through the secretory pathway in DYT1 dystonia cellsProceedings of the National Academy of Sciences, 2007
- Real-time detection and continuous monitoring of ER stress in vitro and in vivo by ES-TRAP: evidence for systemic, transient ER stress during endotoxemiaNucleic Acids Research, 2006
- Quantitative measurement of events in the mammalian unfolded protein responseMethods, 2005
- Endoplasmic Reticulum Stress Links Obesity, Insulin Action, and Type 2 DiabetesScience, 2004
- An improved cyan fluorescent protein variant useful for FRETNature Biotechnology, 2004
- Rapid redistribution of Golgi proteins into the ER in cells treated with brefeldin A: Evidence for membrane cycling from Golgi to ERCell, 1989
- Associations of elements of the Golgi apparatus with microtubules.The Journal of cell biology, 1984
- Cathechol-O-methyltransferase activity in cultured human skin fibroblasts from controls and patients with dystonia musculorum deformansJournal of Neuroscience Research, 1981
- Comparative studies of intracellular transport of secretory proteins.The Journal of cell biology, 1978
- Cytochalasin B: Does It Affect Actin-Like Filaments?Science, 1972