Year: 2020
Type: article
Abstract: Reliance on rodents for understanding pancreatic genetics, development and islet function could limit progress in developing interventions for human diseases such as diabetes mellitus. Similarities of pancreas morphology and function suggest that porcine and human pancreas developmental biology may have useful homologies. However, little is known about pig pancreas development. To fill this knowledge gap, we investigated fetal and neonatal pig pancreas at multiple, crucial developmental stages using modern experimental approaches. Purification of islet β-, α- and δ-cells followed by transcriptome analysis (RNA-seq) and immunohistology identified cell- and stage-specific regulation, and revealed that pig and human islet cells share characteristic features that are not observed in mice. Morphometric analysis also revealed endocrine cell allocation and architectural similarities between pig and human islets. Our analysis unveiled scores of signaling pathways linked to native islet β-cell functional maturation, including evidence of fetal α-cell GLP-1 production and signaling to β-cells. Thus, the findings and resources detailed here show how pig pancreatic islet studies complement other systems for understanding the developmental programs that generate functional islet cells, and that are relevant to human pancreatic diseases.
Source: Development
DOI: 10.1242/dev.186213
Language: English
Subfield: Surgery
Field: Medicine
Domain: Health Sciences
Open Access status: green
Funders: American Diabetes Association, Larry L. Hillblom Foundation, H. L. Snyder Medical Foundation, Stanford Diabetes Research Center, National Institutes of Health, School of Medicine, Stanford University, National Institute of Diabetes and Digestive and Kidney Diseases, National Center for Advancing Translational Sciences
Awards: G1465217466, Spectrum Stanford Center for clinical and Translational Research and Education, Stanford Center for Clinical & Translational Education and Research (Spectrum), G4034131135, G5059582383, G522490644, G9000005647, G9000252654, Stanford Diabetes Research Center, Diabetes, Endocrinology and Metabolism Training Grant
OpenAlex ID: W3007176590
