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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...

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Autores principales: Wang, Gaiping, Chen, Anqi, Wu, Yu, Wang, Danlin, Chang, Cuifang, Yu, Guoying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
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.
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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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