Distinction of leucocyte classes based on chromatin-structure-dependent DNA-binding of 7-aminoactinomycin D

Abstract

Binding of the DNA‐specific dye 7‐aminoactinomycin D (7‐AMD) in chromatin of human leucocytes was studied by flow cytometry. After formaldehyde fixation and permeabilization, monocytes bound 30–130% more 7‐AMD than lymphocytes, while binding in granulocytes was 20–60% higher than in lymphocytes. Monocytes and lymphocytes bound similar amounts of 7‐AMD when cells were permeabilized by detergent prior to fixation. Digestion of DNA in formaldehyde‐fixed chromatin by DNase1 was quantitated by measuring Hoechst 33258 (H33258) fluorescence of mononuclear cells. The monocyte/lymphocyte H33258 fluorescence ratio decreased with DNase1 digestion to an asymptotic value of 0.74, showing that DNA in chromation of monocytes was more susceptible to DNase1 digestion. 7‐AMD binding increased, reached a maximum and then decreased with extent of DNase1 digestion in both mononuclear cell types. The monocyte/lymphocyte 7‐AMD fluorescence ratio also decreased after DNase1 digestion. RNA content and RNA synthesis were higher in monocytes than in lymphocytes. The results show that 7‐AMD binding in chromatin of mononuclear leucocytes correlates with transcriptional activity as measured by DNase1 susceptibility and RNA synthesis. The staining procedure may be used for differential counting of mature myeloid cells in peripheral blood and bone marrow.