首页|T细胞条件性敲除Spi1基因小鼠的繁育及鉴定

T细胞条件性敲除Spi1基因小鼠的繁育及鉴定

Breeding and genotyping of T lymphocyte-conditional Spi1 knockout mice

扫码查看
目的 繁育T细胞条件性敲除Spi1 基因的小鼠并对其进行鉴定,为进一步探索Spi1 编码蛋白PU.1 的作用提供研究基础.方法 将Lck-Cre小鼠与 Spi1flox/flox小鼠进行杂交繁育,通过聚合酶链式反应(PCR)和琼脂糖凝胶电泳鉴定小鼠基因型,筛选出基因型为Lck-Cre×Spi1flox/flox的小鼠即为T细胞条件性敲除Spi1 基因的纯合子小鼠.使用磁珠分选脾脏T淋巴细胞,并应用Western blot、实时荧光定量PCR(qPCR)及流式细胞术检测PU.1 在T细胞中的敲除效率.结果 Lck-Cre×Spi1flox/flox小鼠基因稳定遗传.与Spi1flox/flox小鼠相比,Lck-Cre×Spi1flox/flox小鼠脾脏T细胞中的PU.1 表达水平显著降低.结论 该研究应用 Cre/LoxP 系统和CRISPR/Cas9 技术成功构建了T细胞条件性敲除Spi1 基因小鼠,为后续研究PU.1 在T细胞相关疾病中的具体作用提供了可靠的动物模型.
Objective To breed and identify the T lymphocyte-conditional Spi1 knockout mice for the further in-vestgation of the specific role of Spi1-encoded protein PU.1.Methods The Lck-Cre mice were mated with Spi1flox/flox mice to obtain Lck-Cre×Spi1flox/flox mice(T lymphocyte-specific Spi1 knockout mice),and the genotype was determined by polymerase chain reaction(PCR)and agarose gel electrophoresis.Magnetic beads were used to sort out the splenic T lymphocytes,and the knockdown efficiency of PU.1 in T cells was detected by Western blot,quantitative real-time PCR(qPCR)and flow cytometry.Results The Lck-Cre×Spi1flox/flox mouse genotype was stably inherited.Compared with Spi1flox/flox mice,the expression level of PU.1 was significantly reduced in splenic T cells of Lck-Cre×Spi1flox/flox mice.Conclusion In this study,the T lymphocyte-specific Spi1 knockout mice was successfully constructed by applying Cre/LoxP system and CRISPR/Cas9 technology,which provided a reliable an-imal model for the subsequent experiments of the specific role of PU.1 in T cell-related diseases.

Spi1Cre/LoxP systemCRISPR/Cas9 technologyT cellsPU.1conditional knockout

王卉卉、朱向玲、吴旭铭、张慧茹、周园园、王安琪、刘崇、涂佳杰

展开 >

安徽医科大学临床药理研究所,抗炎免疫药物教育部重点实验室,抗炎免疫药物安徽协同创新中心,合肥 230032

Spi1 Cre/LoxP系统 CRISPR/Cas9技术 T细胞 PU.1 条件性敲除

安徽省高等学校杰出青年科研项目

2022AH020052

2024

安徽医科大学学报
安徽医科大学

安徽医科大学学报

CSTPCD北大核心
影响因子:1.095
ISSN:1000-1492
年,卷(期):2024.59(4)
  • 10