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The Role of INDY in Metabolic Regulation

Reduced expression of the Indy (I'm Not Dead Yet) gene in D. melanogaster and C. elegans extends longevity. Indy and its mammalian homolog mINDY (Slc13a5, NaCT) are transporters of TCA cycle intermediates, mainly handling the uptake of citrate via the plasma membrane into the cytosol. Deletion...

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Detalles Bibliográficos
Autores principales: Willmes, Diana M, Birkenfeld, Andreas L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology (RNCSB) Organization 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3962103/
https://www.ncbi.nlm.nih.gov/pubmed/24688728
http://dx.doi.org/10.5936/csbj.201303020
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author Willmes, Diana M
Birkenfeld, Andreas L
author_facet Willmes, Diana M
Birkenfeld, Andreas L
author_sort Willmes, Diana M
collection PubMed
description Reduced expression of the Indy (I'm Not Dead Yet) gene in D. melanogaster and C. elegans extends longevity. Indy and its mammalian homolog mINDY (Slc13a5, NaCT) are transporters of TCA cycle intermediates, mainly handling the uptake of citrate via the plasma membrane into the cytosol. Deletion of mINDY in mice leads to significant metabolic changes akin to caloric restriction, likely caused by reducing the effects of mINDY-imported citrate on fatty acid and cholesterol synthesis, glucose metabolism and ß-oxidation. This review will provide an overview on different mammalian SLC1 3 family members with a focus on mINDY (SLCl3A5) in glucose and energy metabolism and will highlight the role of mINDY as a putative therapeutic target for the treatment of obesity, non-alcoholic fatty liver disease and type 2 diabetes.
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spelling pubmed-39621032014-03-31 The Role of INDY in Metabolic Regulation Willmes, Diana M Birkenfeld, Andreas L Comput Struct Biotechnol J Review Article Reduced expression of the Indy (I'm Not Dead Yet) gene in D. melanogaster and C. elegans extends longevity. Indy and its mammalian homolog mINDY (Slc13a5, NaCT) are transporters of TCA cycle intermediates, mainly handling the uptake of citrate via the plasma membrane into the cytosol. Deletion of mINDY in mice leads to significant metabolic changes akin to caloric restriction, likely caused by reducing the effects of mINDY-imported citrate on fatty acid and cholesterol synthesis, glucose metabolism and ß-oxidation. This review will provide an overview on different mammalian SLC1 3 family members with a focus on mINDY (SLCl3A5) in glucose and energy metabolism and will highlight the role of mINDY as a putative therapeutic target for the treatment of obesity, non-alcoholic fatty liver disease and type 2 diabetes. Research Network of Computational and Structural Biotechnology (RNCSB) Organization 2013-12-08 /pmc/articles/PMC3962103/ /pubmed/24688728 http://dx.doi.org/10.5936/csbj.201303020 Text en © Willmes and Birkenfeld. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly cited.
spellingShingle Review Article
Willmes, Diana M
Birkenfeld, Andreas L
The Role of INDY in Metabolic Regulation
title The Role of INDY in Metabolic Regulation
title_full The Role of INDY in Metabolic Regulation
title_fullStr The Role of INDY in Metabolic Regulation
title_full_unstemmed The Role of INDY in Metabolic Regulation
title_short The Role of INDY in Metabolic Regulation
title_sort role of indy in metabolic regulation
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3962103/
https://www.ncbi.nlm.nih.gov/pubmed/24688728
http://dx.doi.org/10.5936/csbj.201303020
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