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Fat storage-inducing transmembrane proteins: beyond mediating lipid droplet formation
Fat storage-inducing transmembrane proteins (FITMs) were initially identified in 2007 as members of a conserved endoplasmic reticulum (ER) resident transmembrane protein gene family, and were found to be involved in lipid droplet (LD) formation. Recently, several studies have further demonstrated th...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9644577/ https://www.ncbi.nlm.nih.gov/pubmed/36348306 http://dx.doi.org/10.1186/s11658-022-00391-z |
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author | Wang, Gaiping Chen, Anqi Wu, Yu Wang, Danlin Chang, Cuifang Yu, Guoying |
author_facet | Wang, Gaiping Chen, Anqi Wu, Yu Wang, Danlin Chang, Cuifang Yu, Guoying |
author_sort | Wang, Gaiping |
collection | PubMed |
description | Fat storage-inducing transmembrane proteins (FITMs) were initially identified in 2007 as members of a conserved endoplasmic reticulum (ER) resident transmembrane protein gene family, and were found to be involved in lipid droplet (LD) formation. Recently, several studies have further demonstrated that the ability of FITMs to directly bind to triglyceride and diacylglycerol, and the diphosphatase activity of hydrolyzing fatty acyl-CoA, might enable FITMs to maintain the formation of lipid droplets, engage in lipid metabolism, and protect against cellular stress. Based on the distribution of FITMs in tissues and their important roles in lipid droplet biology and lipid metabolism, it was discovered that FITMs were closely related to muscle development, adipocyte differentiation, and energy metabolism. Accordingly, the abnormal expression of FITMs was not only associated with type 2 diabetes and lipodystrophy, but also with cardiac disease and several types of cancer. This study reviews the structure, distribution, expression regulation, and functionality of FITMs and their potential relationships with various metabolic diseases, hoping to provide inspiration for fruitful research directions and applications of FITM proteins. Moreover, this review will provide an important theoretical basis for the application of FITMs in the diagnosis and treatment of related diseases. |
format | Online Article Text |
id | pubmed-9644577 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-96445772022-11-15 Fat storage-inducing transmembrane proteins: beyond mediating lipid droplet formation Wang, Gaiping Chen, Anqi Wu, Yu Wang, Danlin Chang, Cuifang Yu, Guoying Cell Mol Biol Lett Review Letter Fat storage-inducing transmembrane proteins (FITMs) were initially identified in 2007 as members of a conserved endoplasmic reticulum (ER) resident transmembrane protein gene family, and were found to be involved in lipid droplet (LD) formation. Recently, several studies have further demonstrated that the ability of FITMs to directly bind to triglyceride and diacylglycerol, and the diphosphatase activity of hydrolyzing fatty acyl-CoA, might enable FITMs to maintain the formation of lipid droplets, engage in lipid metabolism, and protect against cellular stress. Based on the distribution of FITMs in tissues and their important roles in lipid droplet biology and lipid metabolism, it was discovered that FITMs were closely related to muscle development, adipocyte differentiation, and energy metabolism. Accordingly, the abnormal expression of FITMs was not only associated with type 2 diabetes and lipodystrophy, but also with cardiac disease and several types of cancer. This study reviews the structure, distribution, expression regulation, and functionality of FITMs and their potential relationships with various metabolic diseases, hoping to provide inspiration for fruitful research directions and applications of FITM proteins. Moreover, this review will provide an important theoretical basis for the application of FITMs in the diagnosis and treatment of related diseases. BioMed Central 2022-11-08 /pmc/articles/PMC9644577/ /pubmed/36348306 http://dx.doi.org/10.1186/s11658-022-00391-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Letter Wang, Gaiping Chen, Anqi Wu, Yu Wang, Danlin Chang, Cuifang Yu, Guoying Fat storage-inducing transmembrane proteins: beyond mediating lipid droplet formation |
title | Fat storage-inducing transmembrane proteins: beyond mediating lipid droplet formation |
title_full | Fat storage-inducing transmembrane proteins: beyond mediating lipid droplet formation |
title_fullStr | Fat storage-inducing transmembrane proteins: beyond mediating lipid droplet formation |
title_full_unstemmed | Fat storage-inducing transmembrane proteins: beyond mediating lipid droplet formation |
title_short | Fat storage-inducing transmembrane proteins: beyond mediating lipid droplet formation |
title_sort | fat storage-inducing transmembrane proteins: beyond mediating lipid droplet formation |
topic | Review Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9644577/ https://www.ncbi.nlm.nih.gov/pubmed/36348306 http://dx.doi.org/10.1186/s11658-022-00391-z |
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