Platelet-activating factor and antagonists modulate DNA synthesis in human bone marrow stromal cell cultures

Frédéric Rougier , Fabienne Dupuis , Elisabeth Cornu , Claude Dulery , Vincent Praloran , Yves Denizot
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引用次数: 13

Abstract

Platelet-activating fator (PAF) is present in the human bone marrow. We have investigated the effect of PAF and antagonists (BN 52021 and CV 3988) on the growth of human marrow stromal cells. PAF (1 μM) stimulates and PAF antagonists (0.1–1 μM) inhibit [3H]thymidine incorporation in cells grown in 5% serum. The catabolism of PAF by stromal cells was inhibited by CV 3988 suggesting the presence of specific PAF receptor on cells. PAF and antagonists (0.1 nM–10 μM) had no effect on cells cultured in high serum concentration (20%) or in low serum concentration (1%) with 0.5 ng/ml of basic fibroblast growth factor (bFGF). This study indicates for the first time that PAF modulates the serum-induced but not the bFGF-induced growth of marrow stromal cells. The interactions between PAF and stromal cells during inflammatory marrow events such as myelofibrosis deserve to be assessed.

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血小板活化因子和拮抗剂在人骨髓基质细胞培养中调节DNA合成
血小板活化因子(PAF)存在于人骨髓中。我们研究了PAF和拮抗剂(BN 52021和CV 3988)对人骨髓基质细胞生长的影响。在5%血清中培养的细胞中,PAF (1 μM)刺激和PAF拮抗剂(0.1-1 μM)抑制[3H]胸苷结合。间质细胞对PAF的分解代谢受到cv3988的抑制,表明细胞上存在特异性的PAF受体。PAF和拮抗剂(0.1 nM-10 μM)对高血清浓度(20%)和低血清浓度(1%)碱性成纤维细胞生长因子(bFGF) 0.5 ng/ml培养的细胞无影响。本研究首次表明PAF可调节血清诱导的骨髓基质细胞生长,而非bfgf诱导的骨髓基质细胞生长。在炎症性骨髓事件(如骨髓纤维化)中,PAF和基质细胞之间的相互作用值得评估。
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