Lawry J, Kristensen S D, Martin J F
Department of Virology, University Medical School, Sheffield.
Clin Lab Haematol. 1989;11(4):361-8. doi: 10.1111/j.1365-2257.1989.tb00234.x.
Megakaryocytes are polyploid cells that constitute less than 0.1% of the nucleated cells in the bone marrow of most mammals including man. The DNA content of megakaryocytes has previously been measured by microdensitometry. Flow cytometry has also been used in the analysis of bone marrow megakaryocytes, but the general prerequisite for prior enrichment has made this technology less attractive. We describe here a modification to the mode of analysis of megakaryocyte DNA content that can be applied to whole, partially purified and elutriated human and rabbit bone marrow. The electronic masking of low-ploidy cells makes it possible to visualize the DNA content of minority, high-ploidy populations of megakaryocytes within a few minutes. In addition, this rapid technique can be combined with monoclonal antibody analysis of bone marrow cells to aid megakaryocyte identification.
巨核细胞是多倍体细胞,在包括人类在内的大多数哺乳动物的骨髓有核细胞中所占比例不到0.1%。巨核细胞的DNA含量此前已通过显微密度测定法进行测量。流式细胞术也已用于骨髓巨核细胞的分析,但预先富集的一般前提使得这项技术吸引力降低。我们在此描述一种对巨核细胞DNA含量分析模式的改进方法,该方法可应用于完整的、部分纯化的以及淘洗过的人类和兔骨髓。对低倍体细胞进行电子屏蔽后,可在几分钟内观察到少数高倍体巨核细胞群体的DNA含量。此外,这种快速技术可与骨髓细胞的单克隆抗体分析相结合,以辅助巨核细胞的鉴定。