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. Author manuscript; available in PMC: 2011 Apr 1.
Published in final edited form as: Drug Discov Today Dis Models. 2010 SPRING;7(1-2):27–33. doi: 10.1016/j.ddmod.2010.11.001

Table 1.

Animal Models of Membranous Nephropathy

Animal Antigen Glomerular Immune Deposits Tubular Immune Deposits Comments Ref
Rat Megalin (PHN) +++P ++P Pro: Currently best model, widely used, nearly identical pathology, easy to produce, short time frame.
Con: PHN antigen (megalin) not found in human MN
[12]
Rat Megalin (AHN) +++P ++P Longer to produce, more variable, more discomfort for rats [1]
Rat DPPIV +T +T Transient model, few immune deposits [31,39]
Mouse Cationic BSA ++P - Best mouse model, limited experience. [32]
Mouse Renal tubular antigen ++P ++P Subepithelial deposits, but minimal proteinuria [33,40]
Mouse Aminopeptidase A ++P +++P Proteinuria marked, but complement independent [34,35]
Rabbit NEP +T - Rarely used [2]
Rabbit DPPIV ++P - Rarely used [41,42]
Rabbit ACE +T +++P Rarely used [41,43,44]
Pig ACE ++P +++P Rarely used [37]

CD26: dipeptidyl peptidase IV, NEP: neutral endopeptidase, P: persistent, large diffuse; T: small focal transient. (Adapted from Table 1 Maruyama S et al, J Am Soc Nephrol 1999[37]).