@article{583da7eb05114b0798e52df536cde224,
title = "Human islets contain four distinct subtypes of β cells",
abstract = "Human pancreatic islets of Langerhans contain five distinct endocrine cell types, each producing a characteristic hormone. The dysfunction or loss of the insulin-producing β cells causes diabetes mellitus, a disease that harms millions. Until now, β cells were generally regarded as a single, homogenous cell population. Here we identify four antigenically distinct subtypes of human β cells, which we refer to as β1-4, and which are distinguished by differential expression of ST8SIA1 and CD9. These subpopulations are always present in normal adult islets and have diverse gene expression profiles and distinct basal and glucose-stimulated insulin secretion. Importantly, the β cell subtype distribution is profoundly altered in type 2 diabetes. These data suggest that this antigenically defined β cell heterogeneity is functionally and likely medically relevant.",
author = "Craig Dorrell and Jonathan Schug and Canaday, {Pamela S.} and Russ, {Holger A.} and Tarlow, {Branden D.} and Grompe, {Maria T.} and Tamara Horton and Matthias Hebrok and Streeter, {Philip R.} and Kaestner, {Klaus H.} and Markus Grompe",
note = "Funding Information: This work was supported by National Institutes of Health HIRN consortium grant UC4 DK104143 (M.G.), grant DK089569 (P.R.S. and K.H.K.), grant DK105831 (M.H.) and grants from the Helmsley Trust (M.G. and M.H.). Human pancreatic islets were provided by the NIDDK-funded Integrated Islet Distribution Program at City of Hope. FACS was performed with the assistance and facilities of the OHSU flow cytometry core. Electron micrographic imaging was performed by Robert J. Kayton, director of the CROET Electron Microscopy Facility at OHSU. Devorah C. Goldman generously provided the MS-1 cell line. Assistance with human c-peptide ELISA assays was provided by Derek K. Zachman.",
year = "2016",
month = jul,
day = "11",
doi = "10.1038/ncomms11756",
language = "English",
volume = "7",
journal = "Nature Communications",
issn = "2041-1723",
publisher = "Nature Publishing Group",
}