人类髓系白血病谱系的两个祖细胞亚群在中央和外周核区域表现出不同的异染色质凝聚状态(附加原始观察的形态学注释)

K. Smetana, H. Klamová, D. Mikulenková, J. Schwarz
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引用次数: 0

摘要

计算机辅助光学图像密度测定表明,骨髓性白血病的特征是根据异染色质凝聚状态(HChCS)分类的两个祖细胞亚群。这些细胞的第一个亚群的特点是核中心区域的HChCS比核周围的大。这种祖细胞似乎具有进一步分化的潜力,主要存在于慢性粒细胞白血病和急性单核细胞白血病的慢性期患者中。祖先的第二个亚群的特点是HChCS在中央和外围核区域都有显著的相似性。在终末分化的粒细胞和单核细胞中也发现了这种相似性。因此,这些祖细胞处于过早终末分化状态,反映了分化过程的改变。这种祖细胞在急性成髓细胞白血病、急性早幼粒细胞白血病和急性髓单细胞白血病中有很大的显性发生率,已知其进一步分化过程发生了改变。
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Two subpopulations of progenitors of leukemic lineages in human myeloid leukemias exhibit different heterochromatin condensation state in central and peripheral nuclear regions (A morphological note with additional original observations)
The computer assisted optical image densitometry indicated that myeloid leukemias were characterized by two subpopulations of progenitor cells classified according to the heterochromatin condensation state (HChCS). The first subpopulation of these cells was characterized by a larger HChCS in the nuclear central regions than in the nuclear periphery. Such progenitors seemed to possess the potential for further differentiation and were predominantly present in patients suffering from the chronic phase of chronic myelocytic and acute monoblastic leukemias. The second subpopulation of progenitors was characterized by a marked similarity of HChCS in both central and peripheral nuclear regions. That similarity was also noted in terminally differentiated granulocytes and monocytes. Thus, these progenitors were in the state of premature terminal differentiation and reflected the altered differentiation process. The large dominant incidence of such progenitors was noted in acute myeloblastic, acute promyelocytic and acute myelomonocytic leukemias with a known alteration of the further differentiation process.
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