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      RNA Sequencing of Single Human Islet Cells Reveals Type 2 Diabetes Genes.

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          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.

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          Author and article information

          Journal
          Cell Metab.
          Cell metabolism
          Elsevier BV
          1932-7420
          1550-4131
          Oct 11 2016
          : 24
          : 4
          Affiliations
          [1 ] Regeneron Pharmaceuticals, Tarrytown, NY 10591, USA.
          [2 ] Regeneron Pharmaceuticals, Tarrytown, NY 10591, USA. Electronic address: jesper.gromada@regeneron.com.
          Article
          S1550-4131(16)30434-X
          10.1016/j.cmet.2016.08.018
          27667665
          d46408bb-95c6-4d5f-9d6a-cdf94df5b588
          History

          glucagon,insulin,pancreatic islet cell,pancreatic polypeptide,single-cell RNA sequencing,somatostatin,type 2 diabetes

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