A Lipid Nanoparticle-Based Method for the Generation of Liver-Specific Knockout Mice

被引:0
作者
Morita, Sumiyo [1 ]
Horii, Takuro [1 ]
Kimura, Mika [1 ]
Kobayashi, Ryosuke [1 ]
Tanaka, Hiroki [2 ]
Akita, Hidetaka [2 ]
Hatada, Izuho [1 ,3 ]
机构
[1] Gunma Univ, Inst Mol & Cellular Regulat, Biosignal Genome Resource Ctr, Lab Genome Sci, 3-39-15 Showa machi, Maebashi 3718512, Japan
[2] Tohoku Univ, Grad Sch Pharmaceut Sci, Lab DDS Design & Drug Disposit, 6-3 Aoba,Aoba ku, Sendai 9808578, Japan
[3] Gunma Univ Initiat Adv Res GIAR, Viral Vector Core, 3-39-15 Showa machi, Gunma 3718511, Japan
关键词
knockout mice; Cre/loxP; lipid nanoparticles (LNPs); DELIVERY; MODEL; RECOMBINATION; DISCOVERY;
D O I
10.3390/ijms241814299
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Knockout mice are useful tools that can provide information about the normal function of genes, including their biochemical, developmental, and physiological roles. One problem associated with the generation of knockout mice is that the loss of some genes of interest produces a lethal phenotype. Therefore, the use of conditioned knockout mice, in which genes are disrupted in specific organs, is essential for the elucidation of disease pathogenesis and the verification of drug targets. In general, conditional knockout mice are produced using the Cre/loxP system; however, the production of the large numbers of Cre/flox knockout and control mice required for analysis requires substantial time and effort. Here, we describe the generation of liver-specific conditional knockout mice via the introduction of lipid nanoparticles encapsulating Cre mRNA into the liver of floxed mice. This technique does not require the production of offspring by mating floxed mice and is therefore more convenient than the conventional method. The results presented here demonstrate that the LNP-based method enables liver-specific gene knockout in a short period of time.
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页数:9
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