Kiss C, Surrey S, Schreiber A D, Schwartz E, McKenzie S E
Division of Hematology, Children's Hospital of Philadelphia, PA 19104, USA.
Exp Hematol. 1996 Aug;24(10):1232-7.
Platelets and megakaryocytes express Fc receptors for IgG which are encoded by the Fc gamma RIIA gene. In an effort to establish a cellular model for induction of Fc gamma RIIA expression during megakaryocyte development by hematopoietic growth factors, steady-state Fc gamma RIIA mRNA levels were monitored in c-kit receptor-positive megakaryocytic cells (M07e, HEL, and Dami) in response to c-kit ligand (KL; also known as stem cell factor, mast cell growth factor, or Steel factor). Northern blot analysis showed that exposure of cells to KL led to significant increases in Fc gamma RIIA levels in M07e (15 x at 24 hours), with smaller increases in HEL (1.9 x at 2 hours) and Dami (1.6 x at 24 hours) cells. K562 cells, which lack c-kit receptor, showed no effect of KL on modulating Fc gamma RIIA mRNA levels. The effects of KL were specific for Fc gamma RIIA, as there were no effects on platelet factor 4 (PF4), gamma-globin, or GATA-1 mRNA levels. Effects of KL, alone and in combination with granulocyte-macrophage colony-stimulating factor (GM-CSF) and gamma-interferon (IFN-gamma), on surface Fc gamma RIIA expression were assessed by flow cytometry using anti-Fc gamma RII monoclonal antibody IV.3. In M07e cells, KL alone and in combination led to significant increases in the percentage of cells positive for surface Fc gamma RIIA and the mean cell fluorescence intensity. Transient transfection studies of an Fc gamma RIIA promoter-luciferase reporter gene in the presence or absence of KL showed increased reporter gene expression in KL-treated cells, with the largest increase (3.7-fold) in the M07e cells. In HEL and Dami cells, other cytokines active in megakaryocytopoiesis when used alone (interleukin-3 [IL-3], IL-6, IL-11, GM-CSF) had negligible activity in increasing reporter gene activity. These results suggest that increased levels of Fc gamma RIIA mRNA after KL treatment of M07e cells are a result, in part, of increased Fc gamma RIIA gene transcription. Our results indicate that M07e cells represent a cellular model for KL-induced Fc gamma RIIA expression in early megakaryocyte development.
血小板和巨核细胞表达由FcγRIIA基因编码的IgG的Fc受体。为了建立一个造血生长因子在巨核细胞发育过程中诱导FcγRIIA表达的细胞模型,研究人员监测了c-kit受体阳性的巨核细胞(M07e、HEL和Dami)中FcγRIIA mRNA的稳态水平,以响应c-kit配体(KL;也称为干细胞因子、肥大细胞生长因子或Steel因子)。Northern印迹分析表明,将细胞暴露于KL会导致M07e细胞中FcγRIIA水平显著增加(24小时时增加15倍),而HEL细胞(2小时时增加1.9倍)和Dami细胞(24小时时增加1.6倍)中增加幅度较小。缺乏c-kit受体的K562细胞,KL对其FcγRIIA mRNA水平的调节没有影响。KL的作用对FcγRIIA具有特异性,因为它对血小板因子4(PF4)、γ-珠蛋白或GATA-1 mRNA水平没有影响。使用抗FcγRII单克隆抗体IV.3通过流式细胞术评估了KL单独以及与粒细胞-巨噬细胞集落刺激因子(GM-CSF)和γ-干扰素(IFN-γ)联合对表面FcγRIIA表达的影响。在M07e细胞中,单独使用KL以及联合使用时均导致表面FcγRIIA阳性细胞百分比和平均细胞荧光强度显著增加。在有或没有KL的情况下对FcγRIIA启动子-荧光素酶报告基因进行瞬时转染研究表明,在经KL处理的细胞中报告基因表达增加,其中M07e细胞中增加幅度最大(3.7倍)。在HEL和Dami细胞中,单独使用时在巨核细胞生成中具有活性的其他细胞因子(白细胞介素-3 [IL-3]、IL-6、IL-11、GM-CSF)在增加报告基因活性方面的活性可忽略不计。这些结果表明,KL处理M07e细胞后FcγRIIA mRNA水平的增加部分是由于FcγRIIA基因转录增加所致。我们的结果表明,M07e细胞代表了KL诱导早期巨核细胞发育中FcγRIIA表达的细胞模型。