Human Epicardial Fat Expresses Glucagon-Like Peptide 1 and 2 Receptors Genes

被引:81
作者
Iacobellis, Gianluca [1 ]
Camarena, Vladimir [2 ]
Sant, David W. [2 ]
Wang, Gaofeng [2 ]
机构
[1] Univ Miami, Miller Sch Med, Dept Med, Div Endocrinol Diabet & Metab, 1400 NW 10th Ave Domin Tower Suite 805 807, Miami, FL 33136 USA
[2] Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, John P Hussman Inst Human Genom, 1400 NW 10th Ave Domin Tower Suite 805 807, Miami, FL 33136 USA
基金
美国国家卫生研究院;
关键词
epicardial fat; epicardial adipose tissue; glucagon-like peptide-1; glucagon-like peptide-2; glucagon-like peptide 1 receptor; ADIPOSE-TISSUE; GLP-1; RECEPTOR; METABOLIC SYNDROME; LIRAGLUTIDE; OBESITY; RNA;
D O I
10.1055/s-0043-109563
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Epicardial adipose tissue (EAT) is an easily measurable visceral fat of the heart with unique anatomy, functionality, and transcriptome. EAT can serve as a therapeutic target for pharmaceutical agents targeting the fat. Glucagon-like peptide-1 (GLP-1) and GLP-2 analogues are newer drugs showing beneficial cardiovascular and metabolic effects. Whether EAT expresses GLP-1 and 2 receptors (GLP-1R and GLP-2R) is unknown. RNA-seq analysis and quantitative real-time polymerase chain reaction (qRT-PCR) were performed to evaluate the presence of GLP-1R and GLP-2R in EAT and subcutaneous fat (SAT) obtained from 8 subjects with coronary artery disease and type 2 diabetes mellitus undergoing elective cardiac surgery. Immunofluorescence was also performed on EAT and SAT samples using Mab3f52 against GLP-1R. Our RNA-sequencing (RNA-seq) analysis showed that EAT expresses both GLP-1R and GLP-2R genes. qRT-PCR analysis confirmed that GLP-1R expression was low but detected by 2 different sets of intron-spanning primers. GLP-2R expression was detected in all patients and was found to be 5-fold higher than GLP-1R. The combination of accurately spliced reads from RNA-seq and successful amplification using intron-spanning primers indicates that both GLP-1R and GLP-2R are expressed in EAT. Immunofluorescence clearly showed that GLP-1R is present and more abundant in EAT than SAT. This is the first time that human EAT is found to express both GLP-1R and GLP-2R genes. Pharmacologically targeting EAT may induce beneficial cardiovascular and metabolic effects.
引用
收藏
页码:625 / 630
页数:6
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