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Updated: Jun 8, 2025

Confocal Imaging of Neuropeptide Y-pHluorin: A Technique to Visualize Insulin Granule Exocytosis in Intact Murine and Human Islets
Published on: September 13, 2017
Decoding Insulin Secretory Granule Maturation Using Genetically Encoded pH Sensors
Wen Lin1, Kaylee Tseng1, Scott E Fraser2
1Department of Chemistry, Bridge Institute, USC Michelson Center for Convergent Bioscience, University of Southern California, Los Angeles, California 90089, United States.
Abstract:
Insulin is a peptide hormone secreted from pancreatic beta cells to regulate blood glucose homeostasis. Maturation of active insulin occurs within insulin secretory granules (ISG) by acidification of the lumen and enzymatic cleavage of insulin before secretion. This process is dysregulated in diabetes, and many questions remain on how the cell controls insulin maturation. We address this gap in knowledge by designing two genetically encoded fluorescence pH sensors and a fluorescence lifetime imaging and analysis pipeline to monitor the pH of individual secretory ISGs within live cells at higher resolution and precision than previously possible. We observed different subpopulations of ISGs based on their pH and subcellular localization. Signals regulating metabolism vs membrane depolarization mobilize different subpopulations of ISGs for secretion, and we confirm that maturation signals acidify ISGs. We conclude that different signaling networks uniquely impact ISG mobilization and secretion. Future applications of these tools will be useful for exploring how these processes are dysregulated in diabetes and provide new paths for developing more effective treatments.
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