人巨噬细胞样细胞系U937的前列腺素生物合成。

M A Cobb, W Hsueh, L M Pachman, W T Barnes
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引用次数: 0

摘要

人巨噬细胞样细胞系U937在外源性花生四烯酸(AA)的作用下产生大量的前列腺素(PG) E2。吲哚美辛(20微克/毫升)预处理可完全抑制PGE2的合成。另一种主要代谢物,在AA孵育过程中释放,不被吲哚美辛抑制,但被去甲双氢愈创木酸(NDGA) (10(-5)M)或BW755C (10(-4)M)降低。这些结果证实了这种巨噬细胞样细胞系中环加氧酶和脂加氧酶活性的存在。用酶聚糖、活化酶聚糖、磷酸肉酸酯(PMA)、热聚集的人IgG (AHG)或钙离子载体A23187刺激U937细胞,均不能刺激PGE2或上述代谢物的合成和释放。U937细胞不能从细胞脂质中释放内源性AA来合成PG,这是U937细胞与正常巨噬细胞的重要功能差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prostaglandin biosynthesis by a human macrophage-like cell line, U937.

The human macrophage-like cell line, U937, produced significant amounts of prostaglandin (PG) E2 when incubated with exogenous arachidonic acid (AA). The synthesis of PGE2 was completely inhibited by pretreatment with indomethacin (20 micrograms/ml). Another major metabolite, unidentified, which was released during incubation with AA, was not inhibited by indomethacin, but was decreased by nordihydroguaiaretic acid (NDGA) (10(-5)M) or BW755C (10(-4)M). These results confirm the presence of cyclooxygenase and perhaps lipoxygenase activities in this macrophage-like cell line. Challenge of U937 cells with zymosan, opsonized zymosan, phorbolmyristate acetate (PMA), heat-aggregated human IgG (AHG), or calcium ionophore A23187 failed to stimulate synthesis and release of either PGE2 or the above mentioned metabolite. The inability of U937 cells to release endogenous AA from cell lipid for PG synthesis constitutes an important functional difference between these cells and normal macrophages.

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