JAK抑制剂阻断干扰素γ减少THP1巨噬细胞源性泡沫细胞胆固醇流出和ATP结合盒转运体A1的表达
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国家自然科学基金资助项目(30470720);;湖南省自然科学基金资助项目(06jj5058)


Transcriptional Profiling of C2C12 Cells Overexpressed Krüppel-Like Factor
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    目的本文观察JAK抑制剂AG490对干扰素γ处理后的THP1巨噬细胞源性泡沫细胞内胆固醇流出和ATP结合盒转运体A1表达的影响。方法用160nmol/L的佛波酯诱导THP1细胞24h,使其贴壁并转化为巨噬细胞,在含有50mg/L氧化型低密度脂蛋白培养液中继续培养细胞48h使其转化为泡沫细胞,以不加任何处理因素的细胞作为空白对照,用干扰素γ单独或联合JAK抑制剂AG490处理细胞24h。油红O染色观察细胞内脂质蓄积情况;液体闪烁计数法观察细胞胆固醇流出....

    Abstract:

    Aim To detect the change of transcriptional profiling of C2C12 cells overexpressed krüppel-like factor 4(KLF4). Methods cDNA chip containing 14000 mouse cDNAs were employed to investigate the expression of genes influenced by KLF4 overexpression in C2C12 cells;bioinformatics database and software such as MEDLINE and Genomatix were performed to analyze the above genes. Results Two hundred and fifity genes were down-regulated in C2C12 cells overexpressed KLF4,with 155 known; Whereas 355 genes were up-regulated,with 255 known.Several genes about inflammatory or apoptosis were included. Conclusion Many downstream genes were influenced by KLF4 overexpression in C2C12 cells.

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郝新瑞,曹冬黎,唐雅玲,胡炎伟,李晓旭,唐朝克. JAK抑制剂阻断干扰素γ减少THP1巨噬细胞源性泡沫细胞胆固醇流出和ATP结合盒转运体A1的表达[J].中国动脉硬化杂志,2007,15(7):566~567.

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  • 收稿日期:2007-03-04
  • 最后修改日期:2007-07-04
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