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Publication : Discordance between GLP-1R gene and protein expression in mouse pancreatic islet cells.

First Author  Gray SM Year  2020
Journal  J Biol Chem Volume  295
Issue  33 Pages  11529-11541
PubMed ID  32554468 Mgi Jnum  J:298945
Mgi Id  MGI:6477901 Doi  10.1074/jbc.RA120.014368
Citation  Gray SM, et al. (2020) Discordance between GLP-1R gene and protein expression in mouse pancreatic islet cells. J Biol Chem 295(33):11529-11541
abstractText  The insulinotropic actions of glucagon-like peptide 1 receptor (GLP-1R) in beta-cells have made it a useful target to manage type 2 diabetes. Metabolic stress reduces beta-cell sensitivity to GLP-1, yet the underlying mechanisms are unknown. We hypothesized that Glp1r expression is heterogeneous among beta-cells and that metabolic stress decreases the number of GLP-1R-positive beta-cells. Here, analyses of publicly available single-cell RNA-Seq sequencing (scRNASeq) data from mouse and human beta-cells indicated that significant populations of beta-cells do not express the Glp1r gene, supporting heterogeneous GLP-1R expression. To check these results, we used complementary approaches employing FACS coupled with quantitative RT-PCR, a validated GLP-1R antibody, and flow cytometry to quantify GLP-1R promoter activity, gene expression, and protein expression in mouse alpha-, beta-, and delta-cells. Experiments with Glp1r reporter mice and a validated GLP-1R antibody indicated that >90% of the beta-cells are GLP-1R positive, contradicting the findings with the scRNASeq data. alpha-cells did not express Glp1r mRNA and delta-cells expressed Glp1r mRNA but not protein. We also examined the expression patterns of GLP-1R in mouse models of metabolic stress. Multiparous female mice had significantly decreased beta-cell Glp1r expression, but no reduction in GLP-1R protein levels or GLP-1R-mediated insulin secretion. These findings suggest caution in interpreting the results of scRNASeq for low-abundance transcripts such as the incretin receptors and indicate that GLP-1R is widely expressed in beta-cells, absent in alpha-cells, and expressed at the mRNA, but not protein, level in delta-cells.
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