Hodgetts J, Hoy T G, Jacobs A
Department of Haematology, University of Wales College of Medicine, Cardiff.
J Clin Pathol. 1988 Oct;41(10):1120-4. doi: 10.1136/jcp.41.10.1120.
A method is described for the measurement of DNA index and cell cycle distribution in purified erythroid and myeloid populations from human bone marrow. Erythroid cells were prepared after complement mediated lysis of non-erythroid marrow cells. Myeloid cells were obtained by fluorescence activated cell sorting by forward and wide angle light scatter. Mononuclear marrow cells were prepared with a density gradient. Nuclei prepared from the separated populations were stained with propidium iodide. Myeloid cells had a higher DNA index than erythroid cells, and the mononuclear preparation had an intermediate value. There were more erythroid than myeloid cells in the S and G2M phases of the cell cycle. These lineage differences are particularly relevant when considering data derived from unseparated bone marrow cells, and further experiments are needed to determine the origin of these anomalies.
本文描述了一种用于测量来自人骨髓的纯化红细胞和髓细胞群体中DNA指数和细胞周期分布的方法。通过补体介导的非红细胞骨髓细胞裂解制备红细胞。通过前向和广角光散射的荧光激活细胞分选获得髓细胞。用密度梯度制备单核骨髓细胞。从分离的群体中制备的细胞核用碘化丙啶染色。髓细胞的DNA指数高于红细胞,单核体制备物的值介于两者之间。在细胞周期的S期和G2M期,红细胞比髓细胞多。在考虑从未分离的骨髓细胞获得的数据时,这些谱系差异尤为重要,需要进一步实验来确定这些异常的来源。