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ABSTRACT: Introduction
Chimeric mice with humanized livers were recently established by transplanting human hepatocytes. This mouse model that is repopulated with functional human hepatocytes could be a useful tool for investigating human hepatic cell biology and drug metabolism and for other preclinical applications. Successfully transplanting human hepatocytes into mice requires that recipient mice with liver failure do not reject these human cells and provide a suitable microenvironment (supportive niche) to promote human donor cell expansion and differentiation. To overcome the limitations of current mouse models, we used Alb-TRECK/SCID mice for in vivo human immature hepatocyte differentiation and humanized liver generation.Methods
1.5 μg/kg diphtheria toxin was administrated in
SUBMITTER: Zhang RR
PROVIDER: S-EPMC4414454 | biostudies-literature | 2015 Mar
REPOSITORIES: biostudies-literature