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CIDE Proteins in Human Health and Disease
Cell death-Inducing DNA Fragmentation Factor Alpha (DFFA)-like Effector (CIDE) proteins have emerged as lipid droplet-associated proteins that regulate fat metabolism. There are three members in the CIDE protein family—CIDEA, CIDEB, and CIDEC (also known as fat-specific protein 27 (FSP27)). CIDEA an...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6468517/ https://www.ncbi.nlm.nih.gov/pubmed/30871156 http://dx.doi.org/10.3390/cells8030238 |
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author | Slayton, Mark Gupta, Abhishek Balakrishnan, Bijinu Puri, Vishwajeet |
author_facet | Slayton, Mark Gupta, Abhishek Balakrishnan, Bijinu Puri, Vishwajeet |
author_sort | Slayton, Mark |
collection | PubMed |
description | Cell death-Inducing DNA Fragmentation Factor Alpha (DFFA)-like Effector (CIDE) proteins have emerged as lipid droplet-associated proteins that regulate fat metabolism. There are three members in the CIDE protein family—CIDEA, CIDEB, and CIDEC (also known as fat-specific protein 27 (FSP27)). CIDEA and FSP27 are primarily expressed in adipose tissue, while CIDEB is expressed in the liver. Originally, based upon their homology with DNA fragmentation factors, these proteins were identified as apoptotic proteins. However, recent studies have changed the perception of these proteins, redefining them as regulators of lipid droplet dynamics and fat metabolism, which contribute to a healthy metabolic phenotype in humans. Despite various studies in humans and gene-targeting studies in mice, the physiological roles of CIDE proteins remains elusive. This review will summarize the known physiological role and metabolic pathways regulated by the CIDE proteins in human health and disease. |
format | Online Article Text |
id | pubmed-6468517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64685172019-04-23 CIDE Proteins in Human Health and Disease Slayton, Mark Gupta, Abhishek Balakrishnan, Bijinu Puri, Vishwajeet Cells Review Cell death-Inducing DNA Fragmentation Factor Alpha (DFFA)-like Effector (CIDE) proteins have emerged as lipid droplet-associated proteins that regulate fat metabolism. There are three members in the CIDE protein family—CIDEA, CIDEB, and CIDEC (also known as fat-specific protein 27 (FSP27)). CIDEA and FSP27 are primarily expressed in adipose tissue, while CIDEB is expressed in the liver. Originally, based upon their homology with DNA fragmentation factors, these proteins were identified as apoptotic proteins. However, recent studies have changed the perception of these proteins, redefining them as regulators of lipid droplet dynamics and fat metabolism, which contribute to a healthy metabolic phenotype in humans. Despite various studies in humans and gene-targeting studies in mice, the physiological roles of CIDE proteins remains elusive. This review will summarize the known physiological role and metabolic pathways regulated by the CIDE proteins in human health and disease. MDPI 2019-03-13 /pmc/articles/PMC6468517/ /pubmed/30871156 http://dx.doi.org/10.3390/cells8030238 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Slayton, Mark Gupta, Abhishek Balakrishnan, Bijinu Puri, Vishwajeet CIDE Proteins in Human Health and Disease |
title | CIDE Proteins in Human Health and Disease |
title_full | CIDE Proteins in Human Health and Disease |
title_fullStr | CIDE Proteins in Human Health and Disease |
title_full_unstemmed | CIDE Proteins in Human Health and Disease |
title_short | CIDE Proteins in Human Health and Disease |
title_sort | cide proteins in human health and disease |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6468517/ https://www.ncbi.nlm.nih.gov/pubmed/30871156 http://dx.doi.org/10.3390/cells8030238 |
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