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Publication : SORCS2 activity in pancreatic α-cells safeguards insulin granule formation and release from glucose-stressed β-cells.

First Author  Kalnytska O Year  2024
Journal  iScience Volume  27
Issue  1 Pages  108725
PubMed ID  38226160 Mgi Jnum  J:351073
Mgi Id  MGI:7575335 Doi  10.1016/j.isci.2023.108725
Citation  Kalnytska O, et al. (2024) SORCS2 activity in pancreatic alpha-cells safeguards insulin granule formation and release from glucose-stressed beta-cells. iScience 27(1):108725
abstractText  Sorting receptor SORCS2 is a stress-response factor protecting neurons from acute insults, such as during epilepsy. SORCS2 is also expressed in the pancreas, yet its action in this tissue remains unknown. Combining metabolic studies in SORCS2-deficient mice with ex vivo functional analyses and single-cell transcriptomics of pancreatic tissues, we identified a role for SORCS2 in protective stress response in pancreatic islets, essential to sustain insulin release. We show that SORCS2 is predominantly expressed in islet alpha cells. Loss of expression coincides with inability of these cells to produce osteopontin, a secreted factor that facilitates insulin release from stressed beta cells. In line with diminished osteopontin levels, beta cells in SORCS2-deficient islets show gene expression patterns indicative of aggravated cell stress, and exhibit defects in insulin granule maturation and a blunted glucose response. These findings corroborate a function for SORCS2 in protective stress response that extends to metabolism.
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