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Mapping histological and functional maturation of human endocrine pancreas across early postnatal periods

Saunders, D. C.; Hart, N.; Pan, F. C.; Reihsmann, C. V.; Hopkirk, A. L.; Izmaylov, N.; Mei, S.; Sherrod, B. A.; Davis, C.; Duryea, J.; Haliyur, R.; Aramandla, R.; Durai, H.; Poffenberger, G.; Martin, A.; Posgai, A. L.; Kusmartseva, I.; Beery, M. L.; Yang, M.; Kang, H.; Greiner, D. L.; Shultz, L. D.; Cartailler, J.-P.; Aamodt, K. I.; Bottino, R.; Atkinson, M. A.; Wright, C. V. E.; Powers, A. C.; Brissova, M.

2024-12-22 developmental biology
10.1101/2024.12.20.629754 bioRxiv
Show abstract

Human endocrine cell differentiation and islet morphogenesis play critical roles in determining islet cell mass and function, but the events and timeline of these processes are incompletely defined. To better understand early human islet cell development and maturation, we collected 115 pediatric pancreata and mapped morphological and spatiotemporal changes from birth through the first ten years of life. Using quantitative analyses and a combination of complementary tissue imaging approaches, including confocal microscopy and whole-slide imaging, we developed an integrated model for endocrine cell formation and islet architecture, including endocrine cell type heterogeneity and abundance, endocrine cell proliferation, and islet vascularization and innervation. We also assessed insulin and glucagon secretory profiles in isolated islet preparations from pediatric donors aged 2 months to 10 years and found a temporal difference in the maturation of insulin secretion compared to glucagon secretion. This comprehensive summary of postnatal and pediatric pancreatic islet development provides a framework for future studies and integration of emerging genetic and genomic data related to islet biology and diabetes risk.

Published in Nature Communications (predicted rank #1) · training set

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