BMJ Open Diabetes Research & Care (Dec 2020)

Genetically engineered pigs manifesting pancreatic agenesis with severe diabetes

  • Eiji Kobayashi,
  • Masaki Nagaya,
  • Koki Hasegawa,
  • Masahito Watanabe,
  • Kazuaki Nakano,
  • Kazutoshi Okamoto,
  • Takeshi Yamada,
  • Ayuko Uchikura,
  • Kenji Osafune,
  • Harumasa Yokota,
  • Taiji Nagaoka,
  • Hitomi Matsunari,
  • Kazuhiro Umeyama,
  • Hiromitsu Nakauchi,
  • Hiroshi Nagashima

DOI
https://doi.org/10.1136/bmjdrc-2020-001792
Journal volume & issue
Vol. 8, no. 2

Abstract

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Introduction Pancreatic duodenum homeobox 1 (Pdx1) expression is crucial for pancreatic organogenesis and is a key regulator of insulin gene expression. Hairy and enhancer of split 1 (Hes1) controls tissue morphogenesis by maintaining undifferentiated cells. Hes1 encodes a basic helix loop helix (bHLH) transcriptional repressor and functionally antagonizes positive bHLH genes, such as the endocrine determination gene neurogenin-3. Here, we generated a new pig model for diabetes by genetic engineering Pdx1 and Hes1 genes.Research design and methods A transgenic (Tg) chimera pig with germ cells carrying a construct expressing Hes1 under the control of the Pdx1 promoter was used to mate with wild-type gilts to obtain Tg piglets.Results The Tg pigs showed perinatal death; however, this phenotype could be rescued by insulin treatment. The duodenal and splenic lobes of the Tg pigs were slender and did not fully develop, whereas the connective lobe was absent. β cells were not detected, even in the adult pancreas, although other endocrine cells were detected, and exocrine cells functioned normally. The pigs showed no irregularities in any organs, except diabetes-associated pathological alterations, such as retinopathy and renal damage.Conclusion Pdx1-Hes1 Tg pigs were an attractive model for the analysis of pancreatic development and testing of novel treatment strategies for diabetes.