PDX1LOW MAFALOW β-cells contribute to islet function and insulin release.

Nasteska D., Fine NHF., Ashford FB., Cuozzo F., Viloria K., Smith G., Dahir A., Dawson PWJ., Lai Y-C., Bastidas-Ponce A., Bakhti M., Rutter GA., Fiancette R., Nano R., Piemonti L., Lickert H., Zhou Q., Akerman I., Hodson DJ.

Transcriptionally mature and immature β-cells co-exist within the adult islet. How such diversity contributes to insulin release remains poorly understood. Here we show that subtle differences in β-cell maturity, defined using PDX1 and MAFA expression, contribute to islet operation. Functional mapping of rodent and human islets containing proportionally more PDX1HIGH and MAFAHIGH β-cells reveals defects in metabolism, ionic fluxes and insulin secretion. At the transcriptomic level, the presence of increased numbers of PDX1HIGH and MAFAHIGH β-cells leads to dysregulation of gene pathways involved in metabolic processes. Using a chemogenetic disruption strategy, differences in PDX1 and MAFA expression are shown to depend on islet Ca2+ signaling patterns. During metabolic stress, islet function can be restored by redressing the balance between PDX1 and MAFA levels across the β-cell population. Thus, preserving heterogeneity in PDX1 and MAFA expression, and more widely in β-cell maturity, might be important for the maintenance of islet function.

DOI

10.1038/s41467-020-20632-z

Type

Journal article

Publication Date

2021-01-01T00:00:00+00:00

Volume

12

Addresses

Institute of Metabolism and Systems Research (IMSR), University of Birmingham, Birmingham, UK.

Keywords

Cells, Cultured, Animals, Mice, Transgenic, Humans, Mice, Diabetes Mellitus, Type 2, Calcium, Homeodomain Proteins, Trans-Activators, Models, Animal, Female, Male, Insulin-Secreting Cells, Maf Transcription Factors, Large, Gene Knock-In Techniques, Primary Cell Culture, Insulin Secretion

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