Àá½Ã¸¸ ±â´Ù·Á ÁÖ¼¼¿ä. ·ÎµùÁßÀÔ´Ï´Ù.
KMID : 1034820180140030255
Molecular & Cellular Toxicology
2018 Volume.14 No. 3 p.255 ~ p.261
Humanized model mice by genome editing and engraftment technologies
Kim Yong-Sam

Ko Jeong-Heon
Abstract
Purpose of review: In drug development, non-clinical studies are performed to evaluate the feasibility, iterative testing and safety of a drug. To harness this process, small animal models which are inexpensive, and easy to breed and maintain such as mice and rats are preferred for non-clinical studies. However, humans and these animals share a large portion of genetic makeup, but genetic and physiological gaps are unavoidable. Efforts to address this innate difference between humans and animals have been made by establishing a so called ¡®humanized¡¯ mouse. In this review, we summarize the scope of the ¡®humanization¡¯ with genome editing technology as well as with cell/ tissue engraftment.

Recent findings: A specifically targeted genetic manipulation became feasible by the development genome editing technologies including zinc finger nucleases (ZFN), transcription activator-like effector nuclease (TALEN), and Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) technology. A humanized animal model can also be generated by engraft human cells or tissues into the corresponding sites of animals. If these two approaches are combined in a synergistic manner, a ¡®humanized mouse¡¯ would be better used for non-clinical study in various experimental and clinical realms.
KEYWORD
Humanized animal model, Genome editing, Engraftment, CRISPR
FullTexts / Linksout information
Listed journal information