Juvonen E, Ruutu T
Third Department of Medicine, University of Helsinki, Finland.
Exp Hematol. 1990 Nov;18(10):1070-2.
In vitro colony formation by erythroid progenitors from the bone marrow was studied in 42 patients with a myelodysplastic syndrome using both a standard assay for growing erythroid colonies and an assay designed for growing megakaryocyte colonies. In the standard assay 5 patients had normal numbers of erythroid burst-forming unit (BFU-E) colonies, 8 showed reduced numbers of colonies, and 29 patients had no colony formation. Six patients with markedly reduced numbers of erythroid colonies or no colonies at all in the standard assay showed normal or increased numbers of erythroid colonies in the megakaryocyte assay. In three of these patients the erythroid colony morphology was normal, whereas the other three showed abundant diffuse growth of erythroid subclusters with no normal colonies. In the other patients, the erythroid culture results were similar in both assays. These results indicate that the impairment of erythroid colony growth seen in most patients with a myelodysplastic syndrome is, at least in a number of patients, not due to reduced numbers of erythroid progenitors but to unusual milieu requirements of abnormal progenitors.
利用用于培养红系集落的标准检测方法和专门用于培养巨核细胞集落的检测方法,对42例骨髓增生异常综合征患者骨髓中的红系祖细胞进行了体外集落形成研究。在标准检测中,5例患者的红系爆式集落形成单位(BFU-E)集落数量正常,8例患者的集落数量减少,29例患者无集落形成。在标准检测中红系集落数量显著减少或完全无集落的6例患者,在巨核细胞检测中红系集落数量正常或增加。其中3例患者的红系集落形态正常,而另外3例则显示红系亚集落大量弥漫性生长,无正常集落。在其他患者中,两种检测的红系培养结果相似。这些结果表明,大多数骨髓增生异常综合征患者中所见的红系集落生长受损,至少在一些患者中,并非由于红系祖细胞数量减少,而是由于异常祖细胞对特殊环境条件的需求。