脂氧素A_4抑制单核巨噬细胞源性树突状细胞的分化及成熟
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Lipoxin A4 Inhibits Lipopolysaccharide-induced Differentiation of RAW264.7 Murine Macrophages into Dendritic-like Cells and Its Maturation
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    摘要:

    目的探讨内源性抗炎症脂质介质脂氧素A4对巨噬细胞向树突状细胞分化及树突状细胞成熟的影响。方法体外培养小鼠巨噬细胞(RAW264.7细胞),根据分组,分别以0μg/L(对照组)、100μg/L的脂多糖、100μg/L的脂多糖联合100 nmol/L或500 nmol/L的脂氧素A4干预小鼠单核巨噬细胞48 h,以流式细胞仪测定细胞表面标记物MHC-II、CD80及CD86的表达,并以激光共聚焦显微镜及相差显微镜观察细胞形态。结果脂氧素A4能显著减少脂多糖刺激下RAW264.7细胞向树突状细胞的转化,并抑制脂多糖刺激下RAW264.7细胞MHC-II及CD86的表达(P<0.01),而对CD80表达无明显影响(P>0.05)。结论脂氧素A4能抑制脂多糖刺激的小鼠巨噬细胞向树突状细胞转化及成熟,可能通过负向调控免疫炎症反而抑制动脉粥样硬化。

    Abstract:

    Aim To investigate the effects of lipoxin A4(LXA4) on lipopolysaccharide(LPS)-induced differentiation and mature of RAW264.7 macrophages into dendritic like cells(DC).Methods RAW264.7 murine macrophages were respectively treated with LPS(0 μg/L and 100 μg/L),LPS(100 μg/L) together with LXA4(100 nmol/L and 500 nmol/L).Cells surface markers(CD80,CD86 and MHC-II) were analyzed by FACS,and cell morphology was observed by laser scanning confocal microscope and phase contrast microscope.Results LPS could significantly promote the differentiation of RAW264.7 murine macrophages into DC and the expression of surface molecules(CD80,CD86,MHC-II)(P<0.01),and LXA4 could inhibit the differentiation of LPS-stimulated RAW264.7 murine macrophages and down-regulate the expression of CD86 and MHC-II,but had no significant effect on the expression of CD80.Conclusion LXA4 could negatively regulate the differentiation of RAW264.7 into DC and inhibit the maturation of DC,which may inhibit the pathogenesis and development of atherosclerosis by negatively regulating immuno-inflammatory response.

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陈样新, 罗年桑, 王晓俏, 林永青, 聂如琼, 王景峰.脂氧素A_4抑制单核巨噬细胞源性树突状细胞的分化及成熟[J].中国动脉硬化杂志,2011,19(5):409~412.

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  • 收稿日期:2010-10-16
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