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Individual islet respirometry reveals functional diversity within the islet population of mice and human donors
OBJECTIVE: Islets from the same pancreas show remarkable variability in glucose sensitivity. While mitochondrial respiration is essential for glucose-stimulated insulin secretion, little is known regarding heterogeneity in mitochondrial function at the individual islet level. This is due in part to...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6157638/ https://www.ncbi.nlm.nih.gov/pubmed/30098928 http://dx.doi.org/10.1016/j.molmet.2018.07.003 |
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author | Taddeo, Evan P. Stiles, Linsey Sereda, Samuel Ritou, Eleni Wolf, Dane M. Abdullah, Muhamad Swanson, Zachary Wilhelm, Josh Bellin, Melena McDonald, Patrick Caradonna, Kacey Neilson, Andrew Liesa, Marc Shirihai, Orian S. |
author_facet | Taddeo, Evan P. Stiles, Linsey Sereda, Samuel Ritou, Eleni Wolf, Dane M. Abdullah, Muhamad Swanson, Zachary Wilhelm, Josh Bellin, Melena McDonald, Patrick Caradonna, Kacey Neilson, Andrew Liesa, Marc Shirihai, Orian S. |
author_sort | Taddeo, Evan P. |
collection | PubMed |
description | OBJECTIVE: Islets from the same pancreas show remarkable variability in glucose sensitivity. While mitochondrial respiration is essential for glucose-stimulated insulin secretion, little is known regarding heterogeneity in mitochondrial function at the individual islet level. This is due in part to a lack of high-throughput and non-invasive methods for detecting single islet function. METHODS: We have developed a novel non-invasive, high-throughput methodology capable of assessing mitochondrial respiration in large-sized individual islets using the XF96 analyzer (Agilent Technologies). RESULTS: By increasing measurement sensitivity, we have reduced the minimal size of mouse and human islets needed to assess mitochondrial respiration to single large islets of >35,000 μm(2) area (∼210 μm diameter). In addition, we have measured heterogeneous glucose-stimulated mitochondrial respiration among individual human and mouse islets from the same pancreas, allowing population analyses of islet mitochondrial function for the first time. CONCLUSIONS: We have developed a novel methodology capable of analyzing mitochondrial function in large-sized individual islets. By highlighting islet functional heterogeneity, we hope this methodology can significantly advance islet research. |
format | Online Article Text |
id | pubmed-6157638 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-61576382018-09-27 Individual islet respirometry reveals functional diversity within the islet population of mice and human donors Taddeo, Evan P. Stiles, Linsey Sereda, Samuel Ritou, Eleni Wolf, Dane M. Abdullah, Muhamad Swanson, Zachary Wilhelm, Josh Bellin, Melena McDonald, Patrick Caradonna, Kacey Neilson, Andrew Liesa, Marc Shirihai, Orian S. Mol Metab Original Article OBJECTIVE: Islets from the same pancreas show remarkable variability in glucose sensitivity. While mitochondrial respiration is essential for glucose-stimulated insulin secretion, little is known regarding heterogeneity in mitochondrial function at the individual islet level. This is due in part to a lack of high-throughput and non-invasive methods for detecting single islet function. METHODS: We have developed a novel non-invasive, high-throughput methodology capable of assessing mitochondrial respiration in large-sized individual islets using the XF96 analyzer (Agilent Technologies). RESULTS: By increasing measurement sensitivity, we have reduced the minimal size of mouse and human islets needed to assess mitochondrial respiration to single large islets of >35,000 μm(2) area (∼210 μm diameter). In addition, we have measured heterogeneous glucose-stimulated mitochondrial respiration among individual human and mouse islets from the same pancreas, allowing population analyses of islet mitochondrial function for the first time. CONCLUSIONS: We have developed a novel methodology capable of analyzing mitochondrial function in large-sized individual islets. By highlighting islet functional heterogeneity, we hope this methodology can significantly advance islet research. Elsevier 2018-07-25 /pmc/articles/PMC6157638/ /pubmed/30098928 http://dx.doi.org/10.1016/j.molmet.2018.07.003 Text en © 2018 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Original Article Taddeo, Evan P. Stiles, Linsey Sereda, Samuel Ritou, Eleni Wolf, Dane M. Abdullah, Muhamad Swanson, Zachary Wilhelm, Josh Bellin, Melena McDonald, Patrick Caradonna, Kacey Neilson, Andrew Liesa, Marc Shirihai, Orian S. Individual islet respirometry reveals functional diversity within the islet population of mice and human donors |
title | Individual islet respirometry reveals functional diversity within the islet population of mice and human donors |
title_full | Individual islet respirometry reveals functional diversity within the islet population of mice and human donors |
title_fullStr | Individual islet respirometry reveals functional diversity within the islet population of mice and human donors |
title_full_unstemmed | Individual islet respirometry reveals functional diversity within the islet population of mice and human donors |
title_short | Individual islet respirometry reveals functional diversity within the islet population of mice and human donors |
title_sort | individual islet respirometry reveals functional diversity within the islet population of mice and human donors |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6157638/ https://www.ncbi.nlm.nih.gov/pubmed/30098928 http://dx.doi.org/10.1016/j.molmet.2018.07.003 |
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