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Sucralose activates an ERK1/2–ribosomal protein S6 signaling axis

The sweetener sucralose can signal through its GPCR receptor to induce insulin secretion from pancreatic β cells, but the downstream signaling pathways involved are not well‐understood. Here we measure responses to sucralose, glucagon‐like peptide 1, and amino acids in MIN6 β cells. Our data suggest...

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Detalles Bibliográficos
Autores principales: Guerra, Marcy L., Kalwat, Michael A., McGlynn, Kathleen, Cobb, Melanie H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5292669/
https://www.ncbi.nlm.nih.gov/pubmed/28174684
http://dx.doi.org/10.1002/2211-5463.12172
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author Guerra, Marcy L.
Kalwat, Michael A.
McGlynn, Kathleen
Cobb, Melanie H.
author_facet Guerra, Marcy L.
Kalwat, Michael A.
McGlynn, Kathleen
Cobb, Melanie H.
author_sort Guerra, Marcy L.
collection PubMed
description The sweetener sucralose can signal through its GPCR receptor to induce insulin secretion from pancreatic β cells, but the downstream signaling pathways involved are not well‐understood. Here we measure responses to sucralose, glucagon‐like peptide 1, and amino acids in MIN6 β cells. Our data suggest a signaling axis, whereby sucralose induces calcium and cAMP, activation of ERK1/2, and site‐specific phosphorylation of ribosomal protein S6. Interestingly, sucralose acted independently of mTORC1 or ribosomal S6 kinase (RSK). These results suggest that sweeteners like sucralose can influence β‐cell responses to secretagogues like glucose through metabolic as well as GPCR‐mediated pathways. Future investigation of novel sweet taste receptor signaling pathways in β cells will have implications for diabetes and other emergent fields involving these receptors.
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spelling pubmed-52926692017-02-07 Sucralose activates an ERK1/2–ribosomal protein S6 signaling axis Guerra, Marcy L. Kalwat, Michael A. McGlynn, Kathleen Cobb, Melanie H. FEBS Open Bio Research Articles The sweetener sucralose can signal through its GPCR receptor to induce insulin secretion from pancreatic β cells, but the downstream signaling pathways involved are not well‐understood. Here we measure responses to sucralose, glucagon‐like peptide 1, and amino acids in MIN6 β cells. Our data suggest a signaling axis, whereby sucralose induces calcium and cAMP, activation of ERK1/2, and site‐specific phosphorylation of ribosomal protein S6. Interestingly, sucralose acted independently of mTORC1 or ribosomal S6 kinase (RSK). These results suggest that sweeteners like sucralose can influence β‐cell responses to secretagogues like glucose through metabolic as well as GPCR‐mediated pathways. Future investigation of novel sweet taste receptor signaling pathways in β cells will have implications for diabetes and other emergent fields involving these receptors. John Wiley and Sons Inc. 2017-01-18 /pmc/articles/PMC5292669/ /pubmed/28174684 http://dx.doi.org/10.1002/2211-5463.12172 Text en © 2016 The Authors. Published by FEBS Press and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Guerra, Marcy L.
Kalwat, Michael A.
McGlynn, Kathleen
Cobb, Melanie H.
Sucralose activates an ERK1/2–ribosomal protein S6 signaling axis
title Sucralose activates an ERK1/2–ribosomal protein S6 signaling axis
title_full Sucralose activates an ERK1/2–ribosomal protein S6 signaling axis
title_fullStr Sucralose activates an ERK1/2–ribosomal protein S6 signaling axis
title_full_unstemmed Sucralose activates an ERK1/2–ribosomal protein S6 signaling axis
title_short Sucralose activates an ERK1/2–ribosomal protein S6 signaling axis
title_sort sucralose activates an erk1/2–ribosomal protein s6 signaling axis
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5292669/
https://www.ncbi.nlm.nih.gov/pubmed/28174684
http://dx.doi.org/10.1002/2211-5463.12172
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