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Role of ACSL5 in fatty acid metabolism
Free fatty acids (FFAs) are essential energy sources for most body tissues. A fatty acid must be converted to fatty acyl-CoA to oxidize or be incorporated into new lipids. Acyl-CoA synthetase long-chain family member 5 (ACSL5) is localized in the endoplasmic reticulum and mitochondrial outer membran...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9932481/ https://www.ncbi.nlm.nih.gov/pubmed/36816310 http://dx.doi.org/10.1016/j.heliyon.2023.e13316 |
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author | Luo, Qin Das, Avash Oldoni, Federico Wu, Panyun Wang, Jiangang Luo, Fei Fang, Zhenfei |
author_facet | Luo, Qin Das, Avash Oldoni, Federico Wu, Panyun Wang, Jiangang Luo, Fei Fang, Zhenfei |
author_sort | Luo, Qin |
collection | PubMed |
description | Free fatty acids (FFAs) are essential energy sources for most body tissues. A fatty acid must be converted to fatty acyl-CoA to oxidize or be incorporated into new lipids. Acyl-CoA synthetase long-chain family member 5 (ACSL5) is localized in the endoplasmic reticulum and mitochondrial outer membrane, where it catalyzes the formation of fatty acyl-CoAs from long-chain fatty acids (C16–C20). Fatty acyl-CoAs are then used in lipid synthesis or β-oxidation mediated pathways. ACSL5 plays a pleiotropic role in lipid metabolism depending on substrate preferences, subcellular localization and tissue specificity. Here, we review the role of ACSL5 in fatty acid metabolism in multiple metabolic tissues, including the liver, small intestine, adipose tissue, and skeletal muscle. Given the increasing number of studies suggesting the role of ACSL5 in glucose and lipid metabolism, we also summarized the effects of ACSL5 on circulating lipids and insulin resistance. |
format | Online Article Text |
id | pubmed-9932481 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-99324812023-02-17 Role of ACSL5 in fatty acid metabolism Luo, Qin Das, Avash Oldoni, Federico Wu, Panyun Wang, Jiangang Luo, Fei Fang, Zhenfei Heliyon Review Article Free fatty acids (FFAs) are essential energy sources for most body tissues. A fatty acid must be converted to fatty acyl-CoA to oxidize or be incorporated into new lipids. Acyl-CoA synthetase long-chain family member 5 (ACSL5) is localized in the endoplasmic reticulum and mitochondrial outer membrane, where it catalyzes the formation of fatty acyl-CoAs from long-chain fatty acids (C16–C20). Fatty acyl-CoAs are then used in lipid synthesis or β-oxidation mediated pathways. ACSL5 plays a pleiotropic role in lipid metabolism depending on substrate preferences, subcellular localization and tissue specificity. Here, we review the role of ACSL5 in fatty acid metabolism in multiple metabolic tissues, including the liver, small intestine, adipose tissue, and skeletal muscle. Given the increasing number of studies suggesting the role of ACSL5 in glucose and lipid metabolism, we also summarized the effects of ACSL5 on circulating lipids and insulin resistance. Elsevier 2023-01-31 /pmc/articles/PMC9932481/ /pubmed/36816310 http://dx.doi.org/10.1016/j.heliyon.2023.e13316 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Review Article Luo, Qin Das, Avash Oldoni, Federico Wu, Panyun Wang, Jiangang Luo, Fei Fang, Zhenfei Role of ACSL5 in fatty acid metabolism |
title | Role of ACSL5 in fatty acid metabolism |
title_full | Role of ACSL5 in fatty acid metabolism |
title_fullStr | Role of ACSL5 in fatty acid metabolism |
title_full_unstemmed | Role of ACSL5 in fatty acid metabolism |
title_short | Role of ACSL5 in fatty acid metabolism |
title_sort | role of acsl5 in fatty acid metabolism |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9932481/ https://www.ncbi.nlm.nih.gov/pubmed/36816310 http://dx.doi.org/10.1016/j.heliyon.2023.e13316 |
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