Krieger M S, Nissen C, Wodnar-Filipowicz A
Department of Research, University Hospital, Basel, Switzerland.
Eur J Haematol. 1995 Apr;54(4):262-9. doi: 10.1111/j.1600-0609.1995.tb00681.x.
In vitro expression of stem-cell factor (SCF) by bone marrow (BM) cells of 30 patients with aplastic anemia (AA) has been analyzed at the mRNA and protein levels. While no deficiencies were found in SCF mRNA expression, low levels of soluble SCF protein were measured in poorly growing AA stroma cultures. The SCF protein concentration in the supernatant and the confluence of AA stroma growth were found to correlate (R = 0.70). Defective proliferation was observed in the majority (20/30) of AA stroma cultures and was paralleled by poor growth of homogeneous cultures of fibroblasts from the same marrow sample. AA stroma growth was enhanced by addition of exogenous SCF in combination with interleukin-11 (IL-11), leukemia inhibitory factor (LIF), and basic fibroblast growth factor (bFGF). Our results demonstrate that deficient growth of stroma cells results in decreased production of SCF. Therefore, SCF and other stroma-derived cytokines may be of therapeutic value in AA patients with documented defects within the BM microenvironment.
对30例再生障碍性贫血(AA)患者骨髓(BM)细胞中干细胞因子(SCF)的体外表达进行了mRNA和蛋白质水平分析。虽然未发现SCF mRNA表达存在缺陷,但在生长不良的AA基质培养物中检测到可溶性SCF蛋白水平较低。发现上清液中SCF蛋白浓度与AA基质生长汇合度相关(R = 0.70)。在大多数(20/30)AA基质培养物中观察到增殖缺陷,并且来自同一骨髓样本的成纤维细胞均质培养物生长不良与之平行。通过添加外源性SCF与白细胞介素-11(IL-11)、白血病抑制因子(LIF)和碱性成纤维细胞生长因子(bFGF)联合使用,可增强AA基质生长。我们的结果表明,基质细胞生长不足导致SCF产生减少。因此,SCF和其他基质衍生的细胞因子可能对骨髓微环境存在明确缺陷的AA患者具有治疗价值。