Wnt4 is heterogeneously activated in maturing β-cells to control calcium signaling, metabolism and function
Year: 2022
Type: article
Abstract: Diabetes is a multifactorial disorder characterized by loss or dysfunction of pancreatic β-cells. β-cells are heterogeneous, exhibiting different glucose sensing, insulin secretion and gene expression. They communicate with other endocrine cell types via paracrine signals and between β-cells via gap junctions. Here, we identify the importance of signaling between β-cells via the extracellular signal WNT4. We show heterogeneity in Wnt4 expression, most strikingly in the postnatal maturation period, Wnt4-positive cells, being more mature while Wnt4-negative cells are more proliferative. Knock-out in adult β-cells shows that WNT4 controls the activation of calcium signaling in response to a glucose challenge, as well as metabolic pathways converging to lower ATP/ADP ratios, thereby reducing insulin secretion. These results reveal that paracrine signaling between β-cells is important in addition to gap junctions in controling insulin secretion. Together with previous reports of WNT4 up-regulation in obesity our observations suggest an adaptive insulin response coordinating β-cells.
Source: Nature Communications
Institutions: University of Copenhagen, Novo Nordisk Foundation, Max Planck Institute of Molecular Cell Biology and Genetics, Helmholtz Munich, German Center for Diabetes Research, Paul Langerhans Institute Dresden, Technische Universität Dresden, Center for Regenerative Therapies Dresden, University of Oulu
Language: English
Subfield: Surgery
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $5,890
OpenAlex ID: W4306989337
