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Human islets contain four distinct subtypes of β cells

  • Craig Dorrell
  • , Jonathan Schug
  • , Pamela S. Canaday
  • , Holger A. Russ
  • , Branden D. Tarlow
  • , Maria T. Grompe
  • , Tamara Horton
  • , Matthias Hebrok
  • , Philip R. Streeter
  • , Klaus H. Kaestner
  • , Markus Grompe
  • Oregon Health and Science University
  • The University of Pennsylvania
  • University of California San Francisco
  • Genentech, Inc

Research output: Contribution to journalArticlepeer-review

311 Scopus citations

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.

Original languageEnglish
Article number11756
JournalNature Communications
Volume7
DOIs
StatePublished - 11 Jul 2016
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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