马志强, 刘力, 成蓓, 王志权. 血管紧张素Ⅱ对巨噬细胞和泡沫细胞ACAT-1及PPAR-γ表达的影响[J]. 心脏杂志, 2011, 23(2): 169-172.
    引用本文: 马志强, 刘力, 成蓓, 王志权. 血管紧张素Ⅱ对巨噬细胞和泡沫细胞ACAT-1及PPAR-γ表达的影响[J]. 心脏杂志, 2011, 23(2): 169-172.
    Effects of angiotensin II on expression of acyl-coenzyme A: cholesterol acyltransferase-1 and peroxisome proliferator-activated receptor-γ in macrophages and foam cells[J]. Chinese Heart Journal, 2011, 23(2): 169-172.
    Citation: Effects of angiotensin II on expression of acyl-coenzyme A: cholesterol acyltransferase-1 and peroxisome proliferator-activated receptor-γ in macrophages and foam cells[J]. Chinese Heart Journal, 2011, 23(2): 169-172.

    血管紧张素Ⅱ对巨噬细胞和泡沫细胞ACAT-1及PPAR-γ表达的影响

    Effects of angiotensin II on expression of acyl-coenzyme A: cholesterol acyltransferase-1 and peroxisome proliferator-activated receptor-γ in macrophages and foam cells

    • 摘要: 目的: 观察血管紧张素Ⅱ(AngⅡ)对巨噬细胞和泡沫细胞过氧化体增殖物激活型受体γ(PPAR-γ)和酰基辅酶A:胆固醇酰基转移酶-1 (ACAT-1)表达的影响。方法: 将单核细胞株THP-1与160 nmol/L佛波酯(PMA)孵育48 h,使之分化为巨噬细胞,继以100 mg/L氧化型低密度脂蛋白(ox-LDL)诱导巨噬细胞分化为泡沫细胞。将巨噬细胞和泡沫细胞用1×10-6 mol/L AngⅡ孵育48 h。运用RT-PCR和Western blot分别检测PPAR-γ mRNA、ACAT-1 mRNA及其蛋白的表达水平。结果: 单核细胞在分化为巨噬细胞和泡沫细胞的过程中,PPAR-γ的表达明显降低(P<0.05),ACAT-1的表达显著增强(P<0.05);经AngⅡ干预后,巨噬细胞和泡沫细胞PPAR-γ的表达进一步降低(P<0.05,P<0.05),而ACAT-1的表达更加增强(P<0.05,P<0.05)。结论: AngⅡ不但可上调巨噬细胞和泡沫细胞中ACAT-1的表达,而且可抑制PPAR-γ的表达。

       

      Abstract: AIM: To investigate the effects of angiotensin II (Ang II) on expression of acyl-coenzyme A: cholesterol acyltransferase-1 (ACAT-1) and peroxisome proliferator-activated receptor-γ (PPAR-γ) in macrophages and foam cells. METHODS: After human THP-1 cells were incubated with 160 nmol/L PMA for 48 h to differentiate into macrophages, the macrophages were cultured with 100 mg/L oxidized LDL for 24 h to differentiate into foam cells. Macrophages and foam cells were incubated with 1×10-6 mol/L Ang II for 48 h. ACAT-1 mRNA and PPAR-γ mRNA were detected by reverse transcription polymerase chain reaction (RT-PCR) and protein levels of ACAT-1 and PPAR-γ were measured by Western blot. RESULTS: ACAT-1 mRNA and protein levels were upregulated significantly (P<0.05) during differentiation from monocytes into macrophages and differentiation from macrophages into foam cells, with the PPAR-γ mRNA and protein levels significantly downregulated (P<0.05). When treated with Ang II, the ACAT-1 mRNA and protein levels of macrophages and foam cells were up-regulated more significantly (P<0.05, P<0.05) and their PPAR-γ mRNA and protein levels were more significantly downregulated (P<0.05, P<0.05). CONCULUSION: Ang II not only significantly promotes ACAT-1 expression but also inhibits PPAR-γ expression during the monocytes-macrophages differentiation.

       

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