Liver-specific Reduction of Mfn2 Protein by RNAi Results in Impaired Glycometabolism and Lipid Homeostasis in BALB/c Mice
10.1007/s11596-009-0603-5
- Author:
CHEN XIAOLIN
1
;
XU YANCHENG
Author Information
1. 武汉大学人民医院
- Keywords:
Mitofusin-2;
RNA interference;
glycometabolism;
lipid homeostasis
- From:
Journal of Huazhong University of Science and Technology (Medical Sciences)
2009;29(6):689-696
- CountryChina
- Language:Chinese
-
Abstract:
Mitofusin-2 (Mfn2) gene expression is positively correlated with insulin sensitivity in patients with type 2 diabetes. However,it is unclear if Mfn2 is involved in carbohydrate metabolism and lipid homeostasis. In order to investigate the specific functions of Mfn2 in glycometabolism and lipid homeostasis in BALB/c mice,a RNA interference technique-mediated hydrodynamic injection was developed,in which short hairpin RNAs (shRNAs) were used to inhibit the Mfn2 expression in vivo. Seventy-two mice were randomly divided into two groups:the Mfn2 reduction group (Mfn2/shRNA) and the negative control group (NC). Intraperitoneal glucose tolerance tests and intraperitoneal insulin tolerance tests were used to evaluate glycometabolism and insulin sensitivity.D-(3-3H) glucose or 3H2O was injected into the tail vein or intraperitoneally to facilitate the calculation of the rate of hepatic glucose production and fatty acid synthesis in vivo. The results showed that,in Mfn2/shRNA mice,the liver Mfn2 protein was significantly decreased,and fasting blood glucose concentrations were increased by approximately 48%,when compared with the NC mice. In parallel with the changes in fasting glucose levels,hepatic glucose production was significantly elevated in Mfn2/shRNA mice. When insulin was administrated,these mice exhibited impaired insulin tolerance.It was also found that the reduction of Mfn2 markedly decreased the rate of fatty acid synthesis in the liver,and the Mfn2/shRNA mice exhibited hypertriglyceridema. Taken together,our results indicate that Mfn2 plays an important role in maintaining glucose and lipid homeostasis,and in the development of insulin resistance in vivo.
