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首页> 外文期刊>Journal of Materials Chemistry, B. materials for biology and medicine >Real-time imaging of cancer cell generations and monitoring tumor growth using a nucleus-targeted red fluorescent probe
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Real-time imaging of cancer cell generations and monitoring tumor growth using a nucleus-targeted red fluorescent probe

机译:使用核靶向红荧光探针的癌细胞代的实时成像和监测肿瘤生长

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摘要

Real-time and long-term nucleus labeling is of great significance for understanding and elucidating cellular and molecular processes in the life sciences, such as gene expression, replication, recombination, and repair, but remains challenging because of the lack of ideal imaging probes. Traditional commercial DNA stains for live-cell imaging either suffer from low water solubility, high cytotoxicity and photobleaching or have small Stokes shifts and low ultraviolet (UV) light excitation; these intrinsic drawbacks limit their utility. Here, a far-red DNA stain (PTB) is explored for in vitro long-term nucleus tracking and in vivo tumor growth monitoring. PTB exhibits a large Stokes shift (similar to 110 nm), far-red emission (625 nm), and a 73.8-fold increase in fluorescence upon binding with DNA. Compared to currently used nucleus stains, PTB also displays low cytotoxicity and good photostability and biocompatibility. More importantly, the results of in vitro studies reveal that PTB can be tracked in stained HepG-2 cancer cells for up to 11 generations. Moreover, PTB demonstrates effective long-term (i.e., 21 days) tumor growth imaging in vivo. The combination of these remarkable properties makes PTB a promising far-red DNA stain.
机译:实时和长期核标记对于理解和阐明生命科学的细胞和分子过程具有重要意义,例如基因表达,复制,重组和修复,但由于缺乏理想的成像探针而仍然挑战。用于活细胞成像的传统商业DNA污渍均患有低水溶性,高细胞毒性和光漂白或具有小的斯托克斯偏移和低紫外线(UV)光励磁;这些内在缺点限制了它们的效用。这里,对体外长期核跟踪和体内肿瘤生长监测探索了远红DNA染色(PTB)。 PTB在与DNA结合时,PTB展现出大型斯托克班(类似于110nm),远红发射(625nm),荧光增加73.8倍。与目前使用的细胞核污渍相比,PTB还显示出低细胞毒性和良好的光稳定性和生物相容性。更重要的是,体外研究的结果表明,可以在染色的HepG-2癌细胞中跟踪PTB,最多11代。此外,PTB证明了体内肿瘤生长成像的有效长期(即21天)。这些显着性质的组合使PTB成为有希望的远红DNA染色。

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