Centre of Experimental Haematology, Department of Medicine (Huddinge), Karolinska Institute, Stockholm, Sweden.
Br J Haematol. 2010 Jun;149(6):844-54. doi: 10.1111/j.1365-2141.2010.08174.x. Epub 2010 Apr 12.
Refractory anaemia with ring sideroblasts (RARS) is characterized by anaemia, erythroid apoptosis, cytochrome c release and mitochondrial ferritin accumulation. Granulocyte-colony-stimulating factor (G-CSF) inhibits the first three of these features in vitro and in vivo. To dissect the molecular mechanisms underlying the RARS phenotype and anti-apoptotic effects of G-CSF, erythroblasts generated from normal (NBM) and RARS marrow CD34(+) cells were cultured +/-G-CSF and subjected to gene expression analysis (GEP). Several erythropoiesis-associated genes that were deregulated in RARS CD34(+) cells showed normal expression in erythroblasts, underscoring the importance of differentiation-specific GEP. RARS erythroblasts showed a marked deregulation of several pathways including apoptosis, DNA damage repair, mitochondrial function and the JAK/Stat pathway. ABCB7, transporting iron from mitochondria to cytosol and associated with inherited ring sideroblast formation was severely suppressed and expression decreased with differentiation, while increasing in NBM cultures. The same pattern was observed for the mitochondrial integrity gene MFN2. Other downregulated key genes included STAT5B, HSPA5, FANCC and the negative apoptosis regulator MAP3K7. Methylation status of key downregulated genes was normal. The mitochondrial pathway including MFN2 was significantly modified by G-CSF, and several heat shock protein genes were upregulated, as evidence of anti-apoptotic protection of erythropoiesis. By contrast, G-CSF had no effect on iron-transport or erythropoiesis-associated genes.
环形铁幼粒细胞难治性贫血(RARS)的特征为贫血、红细胞凋亡、细胞色素 c 释放和线粒体铁蛋白积累。体外和体内实验均表明粒细胞集落刺激因子(G-CSF)可抑制前三种特征。为了剖析 RARS 表型和 G-CSF 抗凋亡作用的分子机制,从正常(NBM)和 RARS 骨髓 CD34+细胞中生成红细胞,并在 +/-G-CSF 培养条件下进行基因表达分析(GEP)。在 RARS CD34+细胞中失调的几个与红细胞生成相关的基因在红细胞中表达正常,这强调了分化特异性 GEP 的重要性。RARS 红细胞显示出几个途径的明显失调,包括凋亡、DNA 损伤修复、线粒体功能和 JAK/Stat 途径。ABCB7 将铁从线粒体转运到细胞质,与遗传性环形铁幼粒细胞形成有关,在 RARS 中严重受抑制,其表达随着分化而降低,而在 NBM 培养物中增加。线粒体完整性基因 MFN2 也观察到相同的模式。其他下调的关键基因包括 STAT5B、HSPA5、FANCC 和负凋亡调节剂 MAP3K7。关键下调基因的甲基化状态正常。G-CSF 显著修饰了线粒体途径,包括 MFN2,并且几个热休克蛋白基因上调,这证明了 G-CSF 对红细胞生成的抗凋亡保护作用。相比之下,G-CSF 对铁转运或与红细胞生成相关的基因没有影响。