Decreased glucagon-like peptide 1 receptor expression in endothelial and smooth muscle cells in diabetic db/db mice: TCF7L2 is a possible regulator of the vascular glucagon-like peptide 1 receptor

被引:18
作者
Kimura, Tomohiko [1 ]
Obata, Atsushi [1 ]
Shimoda, Masashi [1 ]
Okauchi, Seizo [1 ]
Hirukawa, Hidenori [1 ]
Kohara, Kenji [1 ]
Kinoshita, Tomoe [1 ]
Nogami, Yuka [1 ]
Nakanishi, Shuhei [1 ]
Mune, Tomoatsu [1 ]
Kaku, Kohei [2 ]
Kaneto, Hideaki [1 ]
机构
[1] Kawasaki Med Sch, Div Diabet Endocrinol & Metab, Matsushima 577, Kurashiki, Okayama 7010192, Japan
[2] Kawasaki Hosp, Kawasaki Med Sch, Dept Gen Internal Med 1, Okayama, Japan
基金
日本学术振兴会;
关键词
Atherosclerosis; glucagon-like peptide 1 receptor; transcription factor 7-like 2; vascular endothelial cell; vascular smooth muscle cell; glucolipotoxicity; GLP-1; LIRAGLUTIDE; ADHESION; AGONIST;
D O I
10.1177/1479164117725898
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims: Incretin signalling is known to prevent the development of arteriosclerosis by relaxation response in endothelial cells via the glucagon-like peptide 1 receptor. It remains unclear, however, whether vascular glucagon-like peptide 1 receptor expression is altered under some conditions. The aim of this study is to examine whether vascular glucagon-like peptide 1 receptor expression is altered by diabetic state as reported in pancreatic -cells. Methods: We used 18-week-old male diabetic db/db mice and control db/m mice. Excised thoracic artery was specifically collected, and vascular endothelial cells were cultured. We compared the glucagon-like peptide 1 receptor expression levels between the db/db and db/m mice. Results: Metabolic parameters were significantly worse in db/db mice. The glucagon-like peptide 1 receptor and transcription factor 7-like 2 expression levels in endothelial and smooth muscle cells were significantly lower in db/db mice. Furthermore, siRNA to transcription factor 7-like 2 decreased the transcription factor 7-like 2 levels and such reduction of the transcription factor 7-like 2 resulted in the downregulation of the glucagon-like peptide 1 receptor expressions in cultured vascular endothelial cells. Conclusion: The glucagon-like peptide 1 receptor expression level was significantly lower under diabetic condition which was accompanied by the reduction of the transcription factor 7-like 2 expression level. Furthermore, the transcription factor 7-like 2 is a possible regulator of the glucagon-like peptide 1 receptor expression in artery as reported in -cells.
引用
收藏
页码:540 / 548
页数:9
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