Establishment of a mouse model of primary biliary cirrhosis by AMA M2 autoantigen injection.
- Author:
Xiao-hua JIANG
1
;
Ren-qian ZHONG
;
Xiao-yun FANG
;
Feng AN
;
Yin HU
;
Xiu-ping WANG
;
Xian-tao KONG
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Autoantigens; immunology; Disease Models, Animal; Liver Cirrhosis, Biliary; etiology; Mice; Mice, Inbred C57BL; Mitochondria; immunology
- From: Chinese Journal of Hepatology 2006;14(3):202-204
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVESTo establish a primary biliary cirrhosis (PBC) model by AMAM2 autoantigen injection into C57BL/6 mice.
METHODSMice of the model group were immunized intraperitonealy with 200 microl of purified recombinant AMAM2 autoantigen in complete Freund's adjuvant (CFA). Mice immunized with bovine serum albumin and CFA in the same way were used as negative controls. Sixty-six weeks later, mice were sacrificed and their sera were collected. Sera samples were assayed for AMAM2 autoantibody, alkaline phosphatase (ALP), ALT and total bilirubin (TBil). Their liver, stomach, muscle and kidney tissues were sectioned and stained using HE to observe the pathological changes.
RESULTSAntibodies to AMAM2 autoantigen were readily induced in the model group. The mice in the model group had no significant changes in the level of serum ALT and TBil but had an obvious increase of ALP (P<0.05). The stomach, muscle and kidney tissues showed no evident damage while the livers had obvious pathological changes, including bile duct degeneration or proliferation, and mononuclear cell infiltration.
CONCLUSIONThe AMAM2 autoantigen-induced PBC animal model was successfully established in C57BL/6 mice in our experiment and its characteristic biochemical and pathology are quite similar to that in the early stage of human PBC. This model may provide a useful experimental approach for further study of the pathogenesis and clinical treatment of human PBC.