Expression of liver-specific ZP domain-containing protein in mouse models of obesity
10.3969/j.issn.1674-8115.2019.01.003
- Author:
Ye-Qing YUAN
1
Author Information
1. Department of Endocrinology and Metabolism, Shanghai Jiao Tong University, Shanghai Clinical Center for Diabetes
- Publication Type:Journal Article
- Keywords:
Hepatokine;
Liver-specific ZP domain-containing protein;
Obesity
- From:
Journal of Shanghai Jiaotong University(Medical Science)
2019;39(1):11-15
- CountryChina
- Language:Chinese
-
Abstract:
Objective: To study the expression of liver-specific ZP domain-containing protein (LZP) in mouse models of obesity. Methods: The gene and protein expression of LZP in different tissues of C57BL/6J mice were detected by realtime-PCR and Western blotting respectively. C57BL/6J mice were treated with high fat diet (HFD) to establish the model of diet-induced obesity and ob/ob mice were also treated with HFD. The body mass and blood glucose were monitored during the experiment, then the liver weight and fat mass were measured at the end of the study. Hematoxylin-eosin staining of liver was performed to observe the morphology of liver. The expression of LZP in liver of model mice was also detected by realtime-PCR and Western blotting, respectively. Results: The expression of LZP mRNA was mainly found in liver, while a lower gene expression level was also observed in several other tissues such as spleen and testis by realtime-PCR. The protein expression of LZP was detected in liver in C57BL/6J mice by Western blotting. Compared with normal diet group, the group treated with HFD had significantly increased body mass and total fat mass, higher blood glucose, increased liver mass and more serious hepatic steatosis (all P<0.05), while the expression of LZP in liver was reduced (P<0.05). Similarly, body mass and blood glucose were increased significantly in ob/ob mice (both P<0.05), though the expression of LZP was decreased compared with wild type littermates (P<0.05). Conclusion: Mouse models of obesity display decreased expression of LZP in liver, indicating that LZP may play a role in metabolic homeostasis in obese individuals.
