Insulin Promoter-Driven Gaussia Luciferase-Based Insulin Secretion Biosensor Assay for Discovery of β‑Cell Glucose-Sensing Pathways

High throughput screening of insulin secretion is intractable with current methods. We developed a secreted insulin–luciferase system (Ins-GLuc) in β cells that is rapid, inexpensive, and amenable to 96- and 384-well formats. We treated stable Ins-GLuc-expressing MIN6 cells overnight with 6298 marin...

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Bibliographic Details
Published in:ACS sensors Vol. 1; no. 10; pp. 1208 - 1212
Main Authors: Kalwat, Michael A, Wichaidit, Chonlarat, Nava Garcia, Alejandra Y, McCoy, Melissa K, McGlynn, Kathleen, Hwang, In Hyun, MacMillan, John B, Posner, Bruce A, Cobb, Melanie H
Format: Journal Article
Language:English
Published: United States American Chemical Society 28-10-2016
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Summary:High throughput screening of insulin secretion is intractable with current methods. We developed a secreted insulin–luciferase system (Ins-GLuc) in β cells that is rapid, inexpensive, and amenable to 96- and 384-well formats. We treated stable Ins-GLuc-expressing MIN6 cells overnight with 6298 marine natural product fractions. The cells were then washed to remove media and chemicals, followed by stimulation with glucose in the diazoxide paradigm. These conditions allowed the discovery of many insulin secretion suppressors and potentiators. The mechanisms of action of these natural products must be long-lasting given the continuance of secretory phenotypes in the absence of chemical treatment. We anticipate that these natural products and their target pathways will lead to a greater understanding of glucose-stimulated insulin secretion.
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ISSN:2379-3694
2379-3694
DOI:10.1021/acssensors.6b00433