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ORIGINAL RESEARCH article

Front. Endocrinol.

Sec. Cellular Endocrinology

Volume 16 - 2025 | doi: 10.3389/fendo.2025.1640601

An optimized fluorescent reporter enables rapid and cost-effective quantification of regulated secretion from neuroendocrine cells

Provisionally accepted
Theodore  CarterTheodore CarterAlice  McTavishAlice McTavishCedric  S AsensioCedric S Asensio*
  • University of Denver, Denver, United States

The final, formatted version of the article will be published soon.

The ability to quantify protein secretion is critical for studying the secretory pathway. This is particularly important in endocrine cells where dysregulated hormone secretion is associated with the development of diseases such as type 2 diabetes. To measure protein secretion, researchers have previously relied on techniques such as ELISA, RIA and Western blot, which all present limitations, including cost and time consumption. To address these challenges, we developed a plate reader-based assay using an optimized red fluorescent reporter, NPY-sfCherry3c. This reporter showed enhanced expression, proper sorting into secretory granules, and robust secretion from both INS-1 832/13 and PC12 cells. As NPY-sfCherry3c displayed better signal-tobackground ratio compared to previously published reporters (e.g. NPY-GFP, NPY-mCherry), secretion could easily be detected within a few minutes of stimulation, demonstrating the assay's enhanced sensitivity. Our results suggest that NPY-sfCherry3c is a valuable tool to perform rapid and cost-effective secretion assays from neuroendocrine cells.

Keywords: Insulin, regulated secretion, beta cells, Fluorescent reporter, PC12 Cells, INS-1 cells, TIRF, Plate reader

Received: 03 Jun 2025; Accepted: 22 Jul 2025.

Copyright: © 2025 Carter, McTavish and Asensio. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Cedric S Asensio, University of Denver, Denver, United States

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