Correction of hepatosteatosis in humanized liver animals through restoration of il6/il6r/gp130 signaling in human hepatocytes
US-2024130341-A1 · Apr 25, 2024 · US
US9420769B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9420769-B2 |
| Application number | US-201214351481-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 12, 2012 |
| Priority date | Oct 13, 2011 |
| Publication date | Aug 23, 2016 |
| Grant date | Aug 23, 2016 |
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A chimeric non-human animal having an in vivo human hepatocyte population, wherein the effects of non-human animal cells on drug metabolism are suppressed or deleted is provided. A method for producing a chimeric non-human animal that lacks a drug-metabolizing system or has a suppressed drug-metabolizing system and is provided with a drug-metabolizing system driven by human hepatocytes, is provided. The method comprises transplanting human hepatocytes into a non-human animal characterized by (i) being immunodeficient, (ii) having liver damage, and (iii) lacking the functions of an endogenous Cyp3a gene.
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The invention claimed is: 1. A method for producing a chimeric mouse, comprising transplanting a human hepatocyte into a mouse, the mouse (i) being immunodeficient, (ii) having liver damage, and (iii) lacking functions of an endogenous Cyp3a gene, wherein the chimeric mouse lacks a drug-metabolizing system from the mouse and is provided with a drug-metabolizing system driven by human hepatocytes. 2. The method according to claim 1 , wherein the mouse into which a human hepatocyte is to be transplanted is obtained by a method comprising performing three-way crossing of a mouse or offspring thereof having genetic immunodeficiency, a mouse or offspring thereof genetically having liver damage, and a mouse or offspring thereof genetically lacking the functions of the endogenous Cyp3a gene. 3. The method according to claim 1 , wherein the mouse into which a human hepatocyte is to be transplanted is obtained by a method comprising crossing a mouse or offspring thereof having genetic immunodeficiency and genetically having liver damage with a mouse or offspring thereof genetically lacking the functions of the endogenous Cyp3a gene. 4. The method according to claim 1 , wherein the mouse into which a human hepatocyte is to be transplanted is obtained by a method comprising crossing a uPA(+/+)/SCID(+/+) mouse with a cyp3a (KO/KO) mouse, and screening for an animal that homozygously has each genetic component. 5. The method according to claim 1 , wherein the mouse into which a human hepatocyte is to be transplanted is a cyp3a(KO/KO)/uPA(+/+)/SCID(+/+) mouse. 6. A chimeric mouse, obtained by the method according to claim 1 . 7. A chimeric mouse, comprising in vivo human hepatocytes, wherein the chimeric mouse lacks functions of the endogenous Cyp3a gene, and carries the in vivo human hepatocytes. 8. The chimeric mouse according to claim 7 , wherein the non-human animal lacks a drug-metabolizing system and is provided with a drug-metabolizing system driven by human hepatocytes. 9. A method of conducting a toxicity study on a test substance, comprising: administering a test substance to the chimeric mouse according to claim 6 ; and evaluating the effects of the test substance on the human hepatocytes. 10. A method for testing a capacity of human hepatocytes to metabolize a test substance, comprising: administering a test substance to the chimeric mouse according to claim 6 ; and evaluating the capacity of human hepatocytes to metabolize the test substance. 11. A method of conducting a toxicity study on a test substance, comprising: administering a test substance to the chimeric mouse according to claim 7 ; and evaluating the effects of the test substance on the human hepatocytes. 12. A method for testing a capacity of human hepatocytes to metabolize a test substance, comprising: administering a test substance to the chimeric mouse according to claim 7 ; and evaluating the capacity of human hepatocytes to metabolize the test substance.
Liver cells · CPC title
Murine · CPC title
Animal model, e.g. for test or diseases · CPC title
Chimeric vertebrates, e.g. comprising exogenous cells · CPC title
inducing loss of function, i.e. knock out · CPC title
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