| First Author | Resaz R | Year | 2014 |
| Journal | Dis Model Mech | Volume | 7 |
| Issue | 9 | Pages | 1083-91 |
| PubMed ID | 25147298 | Mgi Jnum | J:216511 |
| Mgi Id | MGI:5608933 | Doi | 10.1242/dmm.014878 |
| Citation | Resaz R, et al. (2014) Development of hepatocellular adenomas and carcinomas in mice with liver-specific G6Pase-alpha deficiency. Dis Model Mech 7(9):1083-91 |
| abstractText | Glycogen storage disease type 1a (GSD-1a) is caused by a deficiency in glucose-6-phosphatase-alpha (G6Pase-alpha), and is characterized by impaired glucose homeostasis and a high risk of developing hepatocellular adenomas (HCAs). A globally G6Pase-alpha-deficient (G6pc(-/-)) mouse model that shows pathological features similar to those of humans with GSD-1a has been developed. These mice show a very severe phenotype of disturbed glucose homeostasis and rarely live beyond weaning. We generated liver-specific G6Pase-alpha-deficient (LSG6pc(-/-)) mice as an alternative animal model for studying the long-term pathophysiology of the liver and the potential treatment strategies, such as cell therapy. LSG6pc(-/-) mice were viable and exhibited normal glucose profiles in the fed state, but showed significantly lower blood glucose levels than their control littermates after 6 hours of fasting. LSG6pc(-/-) mice developed hepatomegaly with glycogen accumulation and hepatic steatosis, and progressive hepatic degeneration. Ninety percent of the mice analyzed developed amyloidosis by 12 months of age. Finally, 25% of the mice sacrificed at age 10-20 months showed the presence of multiple HCAs and in one case late development of hepatocellular carcinoma (HCC). In conclusion, LSG6pc(-/-) mice manifest hepatic symptoms similar to those of human GSD-1a and, therefore, represent a valid model to evaluate long-term liver pathogenesis of GSD-1a. |
