Tsuruta T, Tani K, Shimane M, Ozawa K, Takahashi S, Tsuchimoto D, Takahashi K, Nagata S, Sato N, Asano S
Department of Haematology-Oncology, University of Tokyo, Japan.
Br J Haematol. 1996 Jan;92(1):9-22. doi: 10.1046/j.1365-2141.1996.299833.x.
The mRNA expression of alkaline phosphatase (ALP), myeloperoxidase (MPO), defensin and G-CSF receptor (G-CSFR) in bone marrow cells of normal individuals and myeloid disorders, with or without in vitro stimulation by myeloid cell growth factors, i.e. G-CSF, GM-CSF and IL-3, were examined as markers for myeloid cell differentiation in both mononuclear cell (MNC) and polymorphonuclear cell (PMN) fractions. Without any stimulation, ALP mRNA was expressed only in PMNs, G-CSFR mRNA in PMNs were expressed stronger than in MNCs; both MPO and defensin mRNA were expressed to the same degree in both fractions. With stimulation, the ALP mRNA expression in both fractions was strongly enhanced by G-CSF, but the expression was inhibited by GM-CSF and/or IL-3. MPO mRNA expression was stimulated by G-CSF and/or GM-CSF in MNCs. G-CSFR mRNA expression was enhanced by G-CSF in both fractions. Defensin mRNA expression was inhibited by G-CSF. In cases of myelodysplastic syndrome and chronic myelogenous leukaemia which display a suppressed maturation of myeloid cells, our results demonstrated an almost normal response to these growth factors. Our results suggest that studies on these myeloid marker mRNA expressions would provide more knowledge about the differentiation state and cytokine reactivity of myeloid cells in normal individuals as well as various disorders.
在正常个体和骨髓疾病患者的骨髓细胞中,无论有无髓样细胞生长因子(即粒细胞集落刺激因子(G-CSF)、粒细胞-巨噬细胞集落刺激因子(GM-CSF)和白细胞介素-3(IL-3))的体外刺激,碱性磷酸酶(ALP)、髓过氧化物酶(MPO)、防御素和G-CSF受体(G-CSFR)的mRNA表达均作为单核细胞(MNC)和多形核细胞(PMN)组分中髓样细胞分化的标志物进行检测。在无任何刺激的情况下,ALP mRNA仅在PMN中表达,PMN中的G-CSFR mRNA表达强于MNC;MPO和防御素mRNA在两个组分中的表达程度相同。有刺激时,G-CSF强烈增强两个组分中ALP mRNA的表达,但GM-CSF和/或IL-3抑制该表达。G-CSF和/或GM-CSF刺激MNC中MPO mRNA的表达。G-CSF增强两个组分中G-CSFR mRNA的表达。G-CSF抑制防御素mRNA的表达。在骨髓增生异常综合征和慢性粒细胞白血病患者中,髓样细胞成熟受到抑制,我们的结果表明对这些生长因子的反应几乎正常。我们的结果表明,对这些髓样标志物mRNA表达的研究将为正常个体以及各种疾病中髓样细胞的分化状态和细胞因子反应性提供更多知识。