Erba E, Ubezio P, Broggini M, Ponti M, D'Incalci M
Istituto di Ricerche Farmacologiche Mario Negri, Milano, Italy.
Cytometry. 1988 Jan;9(1):1-6. doi: 10.1002/cyto.990090102.
This study was designed to evaluate the effects of vital dye Hoechst 33342 (HO 33342), at concentrations used to obtain a good DNA histogram resolution, on DNA integrity, cell growth, and cell-cycle phase distribution of L1210 cells. HO 33342 exposure for 2 h, at 37 degrees C produced DNA single-strand breaks as assessed by the method of alkaline elution. DNA single-strand breaks were concentration dependent (in the range .5-5 micrograms/ml) and increased significantly when HO 33342 (0.5-1.5 micrograms/ml) was associated with exposure in a flow cytometer to U.V. laser beam illumination. HO 33342 produced a cytotoxic effect on cell growth even at the concentration of 0.5 microgram/ml--a concentration ten-fold smaller than those required to obtain a good DNA histogram resolution. HO 33342 produced a severe block of the cells in the G2-M phase of the cell cycle already evident 24 h after stain exposure and continuing up to 144 h after start of recovery. A new polyploid cell population (with a 4 c DNA content) not present in the unstained cells was already evident 24 h after dye exposure. The data shown in the present paper would imply caution in using sorted cells stained with HO 33342 dye for biological, biomedical, and pharmacological studies.
本研究旨在评估活性染料Hoechst 33342(HO 33342)在用于获得良好DNA直方图分辨率的浓度下,对L1210细胞的DNA完整性、细胞生长和细胞周期阶段分布的影响。通过碱性洗脱法评估,在37℃下暴露于HO 33342 2小时会产生DNA单链断裂。DNA单链断裂呈浓度依赖性(在0.5 - 5微克/毫升范围内),并且当HO 33342(0.5 - 1.5微克/毫升)与在流式细胞仪中暴露于紫外激光束照射相关联时显著增加。即使在0.5微克/毫升的浓度下(该浓度比获得良好DNA直方图分辨率所需的浓度小十倍),HO 33342对细胞生长也产生细胞毒性作用。HO 33342在细胞周期的G2 - M期产生严重的细胞阻滞,在染色暴露后24小时已很明显,并持续到恢复开始后的144小时。在染料暴露后24小时,未染色细胞中不存在的一个新的多倍体细胞群体(具有4c DNA含量)已很明显。本文所示数据表明,在将用HO 33342染料染色的分选细胞用于生物学、生物医学和药理学研究时应谨慎。