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[Establishment of a mouse model of primary biliary cirrhosis by AMA M2 autoantigen injection].

Clinical Laboratory, 85th Hospital of PLA, Shanghai 200052, China.
Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology 03/2006; 14(3):202-4. pp.202-4
Source: PubMed

ABSTRACT To establish a primary biliary cirrhosis (PBC) model by AMAM2 autoantigen injection into C57BL/6 mice.
Mice 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.
Antibodies 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.
The 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.

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Keywords

alkaline phosphatase
 
AMAM2 autoantibody
 
AMAM2 autoantigen
 
AMAM2 autoantigen injection
 
AMAM2 autoantigen-induced PBC animal model
 
bile duct degeneration
 
complete Freund's adjuvant
 
human PBC
 
kidney tissues
 
livers
 
Mice immunized
 
model group
 
mononuclear cell infiltration
 
negative controls
 
pathological changes
 
purified recombinant AMAM2 autoantigen
 
sera
 
Sera samples
 
total bilirubin
 
useful experimental approach
 

Xiao-Hua Jiang