Telford William G, Bradford Jolene, Godfrey William, Robey Robert W, Bates Susan E
Experimental Transplantation and Immunology Branch, National Cancer Institute, Building 10 Room 3-3297, 9000 Rockville Pike, Bethesda, Maryland 20892 USA.
Stem Cells. 2007 Apr;25(4):1029-36. doi: 10.1634/stemcells.2006-0567. Epub 2006 Dec 21.
Hoechst 33342 side population (SP) analysis is a common method for identifying stem cells in mammalian hematopoietic and nonhematopoietic tissues. Although widely employed for stem cell analysis, this method requires an ultraviolet (UV) laser to excite Hoechst 33342. Flow cytometers equipped with UV sources are not common because of the cost of both the laser and optics that can transmit light UV light. Violet laser sources are inexpensive and are now common fixtures on flow cytometers, but have been previously shown to provide insufficient Hoechst dye excitation for consistent resolution of SP cells. One solution to this problem is to identify additional fluorescent substrates with the same pump specificity as Hoechst 33342, but with better violet excitation characteristics. DyeCycle Violet reagent has emission characteristics similar to those of Hoechst 33342, but with a longer wavelength excitation maxima (369 nm). When this dye is loaded into hematopoietic cells, a sharply resolved side population was also observed, similar in appearance to that seen with Hoechst 33342. Unlike Hoechst SP, DCV SP was similar in appearance with both violet and UV excitation. DCV SP could be inhibited fumitremorgin C, and showed the same membrane pump specificity as Hoechst 33342. Simultaneous immunophenotyping with stem cell markers in mouse bone marrow demonstrated that DCV SP was restricted to the stem cell lineage(-) Sca-1(+) c-kit(+) cells population, as is Hoechst SP. Pending confirmation by functional analysis of DCV SP cells, these results suggest that DCV efflux identified approximately the same stem cell population as did Hoechst 33342 efflux. Substituting DCV for Hoechst 33342 in the SP technique may, therefore, allow side population analysis on flow cytometers with violet lasers.
Hoechst 33342 侧群(SP)分析是一种在哺乳动物造血组织和非造血组织中鉴定干细胞的常用方法。尽管该方法广泛用于干细胞分析,但它需要紫外(UV)激光来激发 Hoechst 33342。配备紫外光源的流式细胞仪并不常见,因为激光和能传输紫外光的光学器件成本都很高。紫色激光源价格低廉,现在是流式细胞仪上的常见配置,但先前已表明其对 Hoechst 染料的激发不足以一致地分辨出 SP 细胞。解决这个问题的一种方法是鉴定出与 Hoechst 33342 具有相同泵特异性但具有更好紫色激发特性的其他荧光底物。DyeCycle Violet 试剂具有与 Hoechst 33342 相似的发射特性,但激发最大值波长更长(369 nm)。当将这种染料加载到造血细胞中时,也观察到了清晰分辨的侧群,其外观与用 Hoechst 33342 观察到的相似。与 Hoechst SP 不同,DCV SP 在紫色和紫外激发下外观相似。DCV SP 可被烟曲霉震颤素 C 抑制,并且显示出与 Hoechst 33342 相同的膜泵特异性。在小鼠骨髓中与干细胞标志物同时进行免疫表型分析表明,DCV SP 局限于干细胞谱系(-)Sca-1(+)c-kit(+)细胞群体,Hoechst SP 也是如此。在通过对 DCV SP 细胞进行功能分析确认之前,这些结果表明 DCV 外排鉴定出的干细胞群体与 Hoechst 33342 外排鉴定出的大致相同。因此,在 SP 技术中用 DCV 替代 Hoechst 33342 可能允许在配备紫色激光的流式细胞仪上进行侧群分析。