脂质介质对人髓系和红细胞骨髓祖细胞生长的影响

Fabienne Dupuis, Vanessa Desplat, Vincent Praloran, Yves Denizot
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引用次数: 38

摘要

新鲜分离的人骨髓单核细胞产生脂质化合物,如PAF和白三烯。这些脂质分子在体外通过调节承诺祖细胞(CFU-GM和BFU-E)的生长作用于人骨髓生成和红细胞生成。纳米浓度的白三烯B4和C4刺激人骨髓CFU-GM的生长。相比之下,微摩尔浓度的脂氧合酶抑制剂(NDGA和BW755C)会降低它们的生长,这表明内源性脂氧合酶代谢产物在这一过程中起作用。微摩尔浓度前列腺素E2分别上调和下调骨髓BFU-E和CFU-GM的生长。相反,其他环加氧酶代谢物无影响。最近的研究表明,纳米摩尔浓度的PAF可降低纯化的骨髓CD34+细胞的CFU-GM和BFU-E的生长。综上所述,这些结果表明脂质介质对人的骨髓生成和红细胞生成起作用。然而,目前脂质分子对人骨髓细胞影响的机制和分子信号尚未被探索。
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Effects of lipidic mediators on the growth of human myeloid and erythroid marrow progenitors

Freshly isolated human marrow mononuclear cells produce lipidic compounds such as PAF and leukotrienes. These lipidic molecules act on human marrow myelopoiesis and erythropoiesis by modulating the growth of committed progenitors (CFU-GM and BFU-E) in vitro. Nanomolar concentrations of leukotriene B4 and C4 stimulate the growth of human marrow CFU-GM. In contrast, micromolar concentrations of lipoxygenase inhibitors (NDGA and BW755C) decrease their growth suggesting a role for endogenous lipoxygenase metabolites in this process. Micromolar concentrations of prostaglandin E2 up-regulate and down-regulate the growth of marrow BFU-E and CFU-GM, respectively. In contrast, the other cyclooxygenase metabolites have no effect. Recent studies indicate that nanomolar concentrations of PAF decrease the growth of CFU-GM and BFU-E from purified marrow CD34+ cells. Together these results indicate that lipidic mediators act on human myelopoiesis and erythropoiesis. However at this time the mechanisms and molecular signals mediating the effects of lipidic molecules on human marrow cells are unexplored.

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