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CRISPR/Cas9-mediated ApoE-/- and LDLR-/- double gene knockout in pigs elevates serum LDL-C and TC levels

机译:猪中CRISPR / Cas9介导的ApoE-/-和LDLR-/-双基因敲除可提高血清LDL-C和TC水平

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摘要

The traditional method to establish a cardiovascular disease model induced by high fat and high cholesterol diets is time consuming and laborious and may not be appropriate in all circumstances. A suitable pig model to study metabolic disorders and subsequent atherosclerosis is not currently available. For this purpose, we applied the CRISPR/Cas9 system to Bama minipigs, targeting apolipoprotein E (ApoE) and low density lipoprotein receptor (LDLR) gene simultaneously. Six biallelic knockout pigs of these two genes were obtained successfully in a single step. No off-target incidents or mosaic mutations were detected by an unbiased analysis. Serum biochemical analyses of gene-modified piglets showed that the levels of low density lipoprotein choleserol (LDL-C), total cholesterol (TC) and apolipoprotein B (APOB) were elevated significantly. This model should prove valuable for the study of human cardiovascular disease and related translational research.
机译:建立由高脂肪和高胆固醇饮食诱发的心血管疾病模型的传统方法既费时又费力,可能并不适合所有情况。目前尚没有合适的猪模型来研究代谢紊乱和随后的动脉粥样硬化。为此,我们将CRISPR / Cas9系统应用于巴马小型猪,同时靶向载脂蛋白E(ApoE)和低密度脂蛋白受体(LDLR)基因。一步成功获得了这两个基因的六只双等位基因敲除猪。通过无偏分析未检测到脱靶事件或镶嵌突变。对基因修饰仔猪的血清生化分析表明,低密度脂蛋白胆固醇(LDL-C),总胆固醇(TC)和载脂蛋白B(APOB)的水平显着升高。该模型应被证明对人类心血管疾病的研究和相关的转化研究有价值。

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