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Pancreatic islet β-cell subtypes are derived from biochemically-distinct and nutritionally-regulated islet progenitors

Authors

Brown ME Monica E , Miranda VE Verda E , Nevills S Simone , Hu R Ruiying , Dadi PK Prasanna K , Simmons AJ Alan J , Xu Y Yanwen , Yang Y Yilin , Yagan M Mahircan , Najam S Sadia , Sampson LL Leesa L , Magnuson MA Mark A , Jacobson DA David A , Lau KS Ken S , Hodges E Emily , Gu G Guoqiang .
Nature communications. 2025 7 1; 16(1).
5758

Abstract

Endocrine islet β cells comprise heterogenous subtypes with different gene expression and function levels. Here we study when/how this heterogeneity is induced and how long each subtype maintains its characteristic properties. We show that islet progenitors with distinct gene expression and DNA methylation patterns produce β-cell subtypes of different secretory function, proliferation rate, and viability in male and female mice. These subtypes have differential gene expression that regulates insulin vesicle production or stimulation-secretion coupling and differential DNA methylation in the putative enhancers of these genes. Maternal obesity, a major diabetes risk factor, reduces the proportion of the β-cell subtype with higher levels of glucose responsiveness. The gene signature that defines mouse β-cell subtypes can reliably divide human cells into two sub-populations, with the one having higher predicted glucose responsiveness reduced in diabetic donors. These results suggest that β-cell subtypes can be derived from islet progenitor subsets modulated by maternal nutrition.