| Literature DB >> 27667665 |
Yurong Xin1, Jinrang Kim1, Haruka Okamoto1, Min Ni1, Yi Wei1, Christina Adler1, Andrew J Murphy1, George D Yancopoulos1, Calvin Lin1, Jesper Gromada2.
Abstract
Pancreatic islet cells are critical for maintaining normal blood glucose levels, and their malfunction underlies diabetes development and progression. We used single-cell RNA sequencing to determine the transcriptomes of 1,492 human pancreatic α, β, δ, and PP cells from non-diabetic and type 2 diabetes organ donors. We identified cell-type-specific genes and pathways as well as 245 genes with disturbed expression in type 2 diabetes. Importantly, 92% of the genes have not previously been associated with islet cell function or growth. Comparison of gene profiles in mouse and human α and β cells revealed species-specific expression. All data are available for online browsing and download and will hopefully serve as a resource for the islet research community.Entities:
Keywords: glucagon; insulin; pancreatic islet cell; pancreatic polypeptide; single-cell RNA sequencing; somatostatin; type 2 diabetes
Mesh:
Year: 2016 PMID: 27667665 DOI: 10.1016/j.cmet.2016.08.018
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287