Renner D, Queisser W
Onkologisches Zentrum, Fakultät für klinische Medizin, Universität Heidelberg, BRD.
Acta Haematol. 1988;80(2):74-8. doi: 10.1159/000205606.
To understand abnormal platelet production in chronic granulocytic leukemia, polyploidization and maturation of megakaryocytes in 10 patients were studied using a technique which allows sequential immunofluorescence identification by a monoclonal platelet antibody (C17), cytophotometric determination of the relative DNA content and cytological characterization of megakaryocytes in panoptically stained smears. Compared to normal conditions the proportion of diploid promegakaryocytes was not increased, suggesting an undisturbed influx of progenitor cells into the megakaryocytic cell compartment. Small tetraploid (4c) megakaryocytes undergo maturation without further polyploidization, the so-called microkaryocytes being mature rather than immature cells. Most of the megakaryocytes show rhythmical polyploidization only up to octoploid (8c) level, indicating the inability to produce high-polyploidy cells.
为了解慢性粒细胞白血病中血小板生成异常的情况,采用一种技术对10例患者的巨核细胞多倍体化和成熟过程进行了研究。该技术可通过单克隆血小板抗体(C17)进行连续免疫荧光鉴定,通过细胞光度测定相对DNA含量,并在全景染色涂片中对巨核细胞进行细胞学特征分析。与正常情况相比,二倍体早幼巨核细胞的比例没有增加,这表明祖细胞向巨核细胞区室的流入未受干扰。小四倍体(4c)巨核细胞不经进一步多倍体化即可成熟,所谓的微核细胞是成熟细胞而非未成熟细胞。大多数巨核细胞仅在八倍体(8c)水平之前呈现节律性多倍体化,这表明其无法产生高多倍体细胞。