内科学
内分泌学
免疫组织化学
单克隆抗体
胰腺
肌间神经丛
肠内分泌细胞
生物
受体
十二指肠
胃
抗体
医学
激素
内分泌系统
免疫学
作者
Charles Pyke,R. Scott Heller,Rikke Kaae Kirk,Cathrine Ørskov,Steffen Reedtz‐Runge,Peter Kaastrup,Anders Hvelplund,Linda Bardram,Dan Calatayud,Lotte Bjerre Knudsen
出处
期刊:Endocrinology
[The Endocrine Society]
日期:2014-01-27
卷期号:155 (4): 1280-1290
被引量:661
摘要
Glucagon-like peptide 1 (GLP-1) analogs are increasingly being used in the treatment of type 2 diabetes. It is clear that these drugs lower blood glucose through an increase in insulin secretion and a lowering of glucagon secretion; in addition, they lower body weight and systolic blood pressure and increase heart rate. Using a new monoclonal antibody for immunohistochemistry, we detected GLP-1 receptor (GLP-1R) in important target organs in humans and monkeys. In the pancreas, GLP-1R was predominantly localized in β-cells with a markedly weaker expression in acinar cells. Pancreatic ductal epithelial cells did not express GLP-1R. In the kidney and lung, GLP-1R was exclusively expressed in smooth muscle cells in the walls of arteries and arterioles. In the heart, GLP-1R was localized in myocytes of the sinoatrial node. In the gastrointestinal tract, the highest GLP-1R expression was seen in the Brunner's gland in the duodenum, with lower level expression in parietal cells and smooth muscle cells in the muscularis externa in the stomach and in myenteric plexus neurons throughout the gut. No GLP-1R was seen in primate liver and thyroid. GLP-1R expression seen with immunohistochemistry was confirmed by functional expression using in situ ligand binding with 125I-GLP-1. In conclusion, these results give important new insight into the molecular mode of action of GLP-1 analogs by identifying the exact cellular localization of GLP-1R.
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