GLP-1 receptor localization in monkey and human tissue: novel distribution revealed with extensively validated monoclonal antibody.
Endocrinology · 2014
Last updated 2026-05-28A new study found GLP-1 receptors in several organs of humans and monkeys, including the pancreas, kidneys, lungs, heart, and digestive tract. In the pancreas, these receptors were mostly in insulin-producing cells, while in the heart, they were in cells of the sinoatrial node, which controls heart rhythm. The receptors were absent in the liver and thyroid. The findings were confirmed using two different methods.
AI summary of the abstract below.
| Journal | Endocrinology, 2014 |
|---|---|
| Citations | 696 |
| Relative citation ratio | 23.48 |
| NIH percentile | 100 |
| Molecules | — |
Abstract
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 (125)I-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.
Verbatim abstract via PubMed 24467746 ↗