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Publication : Iron overload in aging <i>Bmp6<sup>‑/‑</sup></i> mice induces exocrine pancreatic injury and fibrosis due to acinar cell loss.

First Author  Pauk M Year  2021
Journal  Int J Mol Med Volume  47
Issue  4 PubMed ID  33649802
Mgi Jnum  J:305102 Mgi Id  MGI:6681952
Doi  10.3892/ijmm.2021.4893 Citation  Pauk M, et al. (2021) Iron overload in aging Bmp6(/) mice induces exocrine pancreatic injury and fibrosis due to acinar cell loss. Int J Mol Med 47(4):1-8
abstractText  The relationship between hemochromatosis and diabetes has been well established, as excessive iron deposition has been reported to result in impaired function of the endocrine and exocrine pancreas. Therefore, the objective of the present study was to analyze the effects of iron accumulation on the pancreata and glucose homeostasis in a bone morphogenetic protein 6knockout (Bmp6(/)) mouse model of hemochromatosis. The sera and pancreatic tissues of wildtype (WT) and Bmp6(/) mice (age, 3 and 10 months) were subjected to biochemical and histological analyses. In addition, (18)Ffluorodeoxyglucose biodistribution was evaluated in the liver, muscle, heart, kidney and adipose tissue of both animal groups. The results demonstrated that 3monthold Bmp6(/) mice exhibited iron accumulation preferentially in the exocrine pancreas, with no signs of pancreatic injury or fibrosis. No changes were observed in the glucose metabolism, as pancreatic islet diameter, insulin and glucagon secretion, blood glucose levels and glucose uptake in the liver, muscle and adipose tissue remained comparable with those in the WT mice. Aging Bmp6(/) mice presented with progressive iron deposits in the exocrine pancreas, leading to pancreatic degeneration and injury that was characterized by acinar atrophy, fibrosis and the infiltration of inflammatory cells. However, the aging mice exhibited unaltered blood glucose levels and islet structure, normal insulin secretion and moderately increased alphacell mass compared with those in the agematched WT mice. Additionally, iron overload and pancreatic damage were not observed in the aging WT mice. These results supported a pathogenic role of iron overload in aging Bmp6(/) mice leading to ironinduced exocrine pancreatic deficiency, whereas the endocrine pancreas retained normal function.
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