Transcriptomic heterogeneity of non-beta islet cells is associated with type 2 diabetes development in mouse models
2024

Non-Beta Cell Diversity in Type 2 Diabetes

Sample size: 126 publication 10 minutes Evidence: moderate

Author Information

Author(s): Gottmann Pascal, Speckmann Thilo, Stadion Mandy, Chawla Prateek, Saurenbach Judith, Ninov Nikolay, Lickert Heiko, Schürmann Annette

Primary Institution: German Institute of Human Nutrition Potsdam-Rehbruecke (DIfE), Nuthetal, Germany

Hypothesis

The aim of this work was to understand the role of non-beta cells in pancreatic islets at early stages of type 2 diabetes pathogenesis.

Conclusion

The transcriptional heterogeneity of non-beta cells impacts intra-islet communication and contributes to beta cell dysfunction.

Supporting Evidence

  • 133 genes associated with human diabetes were differentially expressed in islet cell types.
  • NZO mice showed signs of cellular stress in alpha cells.
  • Delta cells from OB mice had higher somatostatin secretion compared to NZO mice.
  • Macrophages were more abundant in OB mice and communicated extensively with beta cells.

Takeaway

This study shows that different types of cells in the pancreas behave differently in diabetes, which can affect how well insulin is produced.

Methodology

Single-cell RNA sequencing was used to analyze islet cells from obese mouse models with different diabetes susceptibilities.

Limitations

The study primarily relies on transcriptomics, with limited validation at the protein level.

Participant Demographics

Male NZO and B6 mice were used in the study.

Digital Object Identifier (DOI)

10.1007/s00125-024-06301-6

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