G-protein coupled receptors (GPCRs) are essential for islet function, but most studies use rodent islets due to limited human islet availability. We have systematically compared the GPCR mRNA expression in human and mouse islets to determine to what extent mouse islets can be used as surrogates for human islets to study islet GPCR function, and we have identified species-specific expression of several GPCRs. The A receptor (ADORA3) was expressed only in mouse islets and the A agonist MRS 5698 inhibited glucose-induced insulin secretion from mouse islets, with no effect on human islets. Similarly, mRNAs encoding the galanin receptors GAL (GALR1), GAL (GALR2) and GAL GALR3) were abundantly expressed in mouse islets but present only at low levels in human islets, so that it reads (GALR3) and galanin inhibited insulin secretion only from mouse islets. Conversely, the sst1 receptor (SSTR1) was abundant only in human islets and its selective activation by CH 275 inhibited insulin secretion from human islets, with no effect on mouse islets. Our comprehensive human and mouse islet GPCR atlas has demonstrated that species differences do exist in islet GPCR expression and function, which are likely to impact on the translatability of mouse studies to the human context.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5395952PMC
http://dx.doi.org/10.1038/srep46600DOI Listing

Publication Analysis

Top Keywords

mouse islets
28
human islets
20
islets
13
human mouse
12
islet gpcr
12
insulin secretion
12
human
10
mouse
10
mouse islet
8
g-protein coupled
8

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!