CIDE Proteins in Human Health and Disease

被引:40
|
作者
Slayton, Mark [1 ,2 ]
Gupta, Abhishek [1 ,2 ]
Balakrishnan, Bijinu [1 ,2 ]
Puri, Vishwajeet [1 ,2 ]
机构
[1] Ohio Univ, Heritage Coll Osteopath Med, Dept Biomed Sci, Athens, OH 45701 USA
[2] Ohio Univ, Heritage Coll Osteopath Med, Inst Diabet, Athens, OH 45701 USA
关键词
CIDEA; CIDEB; FSP27; fat metabolism; lipid droplets; adipose; liver; FAT-SPECIFIC PROTEIN-27; ALPHA-LIKE EFFECTOR; ADIPOCYTE-SPECIFIC GENE; LIPID DROPLET GROWTH; PPAR-GAMMA; INSULIN SENSITIVITY; TRANSCRIPTIONAL REGULATION; DIFFERENTIAL ROLES; HEPATIC STEATOSIS; ADIPOSE-TISSUE;
D O I
10.3390/cells8030238
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
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页数:14
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