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巨噬细胞特异性敲除TSC1小鼠的构建

Construction of macrophage-specific knockout TSC1 mice
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摘要 目的为研究TSC1在巨噬细胞极化中的作用,拟建立巨噬细胞特异性敲除TSC1小鼠,提供稳定的动物模型。方法利用Cre-loxP系统构建巨噬细胞特异性敲除TSC1小鼠(LysM-Cre TSC1flox/flox),并通过PCR和Western-Blot鉴定模型建立是否成功。结果通过PCR和Western-Blot鉴定LysM-Cre TSC1flox/flox模型建立成功,mTOR活性明显升高。结论成功构建巨噬细胞特异性敲除TSC1小鼠,为TSC1在巨噬细胞极化中的作用研究提供实验基础。 Objective To study the role of TSC1 in macrophage polarization in order to establish a macrophage-specific knockout TSC1 mice and to provide a stable animal model.Methods The Cre-loxP system was used to construct a macrophage-specific knockout TSC1 mice(LysM-Cre TSC1flox/flox),and the model was established by PCR and Western-Blot.Results The LysM-Cre TSC1flox/flox model was established by PCR and western-blot successfully,and the mTOR activity was significantly increased in the model.Conclusion The macrophage-specific knockout TSC1 mice is successfully constructed and it can provide an experimental basis for the role of TSC1 in macrophage polarization.
作者 刘小琳 梁康檐 LIU Xiaolin;LIANG Kangyan(Department of Cell Biology,School of Basic Medical Sciences,Southern Medical University,Guangzhou 510515,China)
出处 《宁夏医学杂志》 CAS 2020年第5期385-387,I0001,共4页 Ningxia Medical Journal
基金 国家自然科学青年基金项目(81402373)。
关键词 结节性硬化复合物1 巨噬细胞 MTOR 基因敲除 TSC1 Macrophage mTOR Gene knockout
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