Dunstan R A
Br J Haematol. 1986 Mar;62(3):587-93. doi: 10.1111/j.1365-2141.1986.tb02971.x.
An indirect immunofluorescence technique with single and double labelling has been used to examine cultured human megakaryocytes for ABH antigens. This technique demonstrated the presence of these antigens on megakaryocytes and a population of small mononuclear cells that probably represent the differentiated precursors of megakaryocytes. In contrast to the intense homogeneous labelling with human anti-PlA1, the labelling with human anti-A, mouse monoclonal anti-A and anti-type 2H is light and heterogeneous, with many cells staining weakly or not at all. This variability in blood group ABH surface antigen expression appears to occur at the level of cell proliferation within colonies. While cells within an individual colony are homogeneous in fluorescence intensity, there is considerable variation between colonies. The progeny of individual megakaryocytes also appear uniform in ABH antigen expression.
采用单标和双标的间接免疫荧光技术检测培养的人巨核细胞中的ABH抗原。该技术证明这些抗原存在于巨核细胞和一群小的单核细胞上,这些小的单核细胞可能代表巨核细胞的分化前体。与人类抗PlA1产生的强烈均匀标记不同,人类抗A、小鼠单克隆抗A和抗2H型的标记较弱且不均匀,许多细胞染色较弱或根本不染色。血型ABH表面抗原表达的这种变异性似乎发生在集落内的细胞增殖水平。虽然单个集落内的细胞在荧光强度上是均匀的,但不同集落之间存在相当大的差异。单个巨核细胞的后代在ABH抗原表达上也显得一致。