Hirons G T, Fawcett J J, Crissman H A
Life Sciences Division, Los Alamos National Laboratory, New Mexico 87545.
Cytometry. 1994 Feb 1;15(2):129-40. doi: 10.1002/cyto.990150206.
Flow cytometric (FCM) studies were performed on nuclei, ethanol-fixed CHO cells, and isolated human GM130 chromosomes stained with two new cyanine dyes, TOTO and YOYO. These fluorochromes, which are dimers of thiazole orange and oxazole yellow, respectively, have high quantum efficiencies and exhibit specificities for both DNA and RNA. Bound to dsDNA in solution, TOTO and YOYO emit at 530 and 510 nm, respectively, when excited at 488 nm and 457 nm, wavelengths available from most lasers employed in FCM. RNase-treated CHO nuclei, stained with either TOTO or YOYO, provided DNA histograms, with low coefficients of variation, that were as good as or better than those obtained with nuclei stained with propidium iodide (PI) or mithramycin (MI). In addition, by comparison on an equimolar basis, nuclei stained with YOYO fluoresced over 1,000 times more intensely than nuclei stained with MI. Fluorescence ratio analyses of nuclei stained with both YOYO and Hoechst 33258 showed that the ratio of YOYO to Hoechst fluorescence remained relatively constant for G1 and S phase cells, but decreased significantly for cells in G2/M. These results indicate that the cyanine dyes may be useful in examining specific changes in chromatin structure during G2/M phases of the cell cycle. Ethanol-fixed CHO cells stained with TOTO or YOYO did not yield reproducible DNA histograms of good quality, presumably because of the poor accessibility of DNA to these large fluorochromes. However, bivariate analyses of human GM130 chromosomes stained with TOTO or YOYO alone and excited sequentially with uv and visible wave-lengths showed resolution of many individual chromosome peaks similar to results obtained for chromosomes stained with HO and chromomycin A3. Collectively, these studies show potential advantages for the use of these new cyanine dyes in FCM studies that require the sensitive detection of DNA.
运用流式细胞术(FCM)对细胞核、乙醇固定的CHO细胞以及用两种新型花青染料TOTO和YOYO染色的分离的人类GM130染色体进行了研究。这些荧光染料分别是噻唑橙和恶唑黄的二聚体,具有高量子效率,并且对DNA和RNA均具有特异性。在溶液中与双链DNA结合时,当在488nm和457nm(大多数FCM所用激光器可提供的波长)激发时,TOTO和YOYO分别在530nm和510nm处发射荧光。用TOTO或YOYO染色的经核糖核酸酶处理的CHO细胞核提供了变异系数低的DNA直方图,其质量与用碘化丙啶(PI)或光神霉素(MI)染色的细胞核所获得的直方图一样好或更好。此外,在等摩尔基础上进行比较时,用YOYO染色的细胞核发出的荧光比用MI染色的细胞核强1000多倍。对用YOYO和Hoechst 33258染色的细胞核进行荧光比率分析表明,对于G1期和S期细胞,YOYO与Hoechst荧光的比率保持相对恒定,但对于G2/M期细胞则显著下降。这些结果表明,花青染料可能有助于检测细胞周期G2/M期染色质结构的特定变化。用TOTO或YOYO染色的乙醇固定的CHO细胞未产生质量良好的可重复DNA直方图,可能是因为这些大的荧光染料难以接近DNA。然而,对仅用TOTO或YOYO染色并依次用紫外和可见光波长激发的人类GM130染色体进行双变量分析,显示出许多单个染色体峰的分辨率,类似于用HO和放线菌素A3染色的染色体所获得的结果。总的来说,这些研究表明,在需要灵敏检测DNA的FCM研究中使用这些新型花青染料具有潜在优势。