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首页> 外文期刊>The Journal of Nuclear Medicine >Single-Cell Characterization of F-18-FLT Uptake with Radioluminescence Microscopy
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Single-Cell Characterization of F-18-FLT Uptake with Radioluminescence Microscopy

机译:放射荧光显微镜对F-18-FLT摄取的单细胞表征

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The radiotracer 3'-deoxy-3'-F-18-fluorothymidine (F-18-FLT) is commonly used to measure cell proliferation in vivo. As a marker of cell proliferation, F-18-FLT is expected to be differentially taken up by arrested and actively dividing cells, but PET measures only aggregate uptake by tumor cells and therefore the single-cell distribution of F-18-FLT is unknown. We used a novel in vitro radioluminescence microscopy technique to measure the differential distribution of F-18-FLT radiotracer with single-cell precision. Methods: Using radioluminescence microscopy, we imaged the absolute uptake of F-18-FLT in live MDA-MB-231 cells grown under different serum conditions. We then compared F-18-FLT uptake with a standard measure of cell proliferation, using fluorescence microscopy of 5-ethynyl-2'-deoxyuridine incorporation in fixed cells. Results: According to 5-ethynyl-2'-deoxyuridine staining, few cells (1%) actively cycled under serum deprivation whereas most of them (71%) did under 20% serum. The distribution of F-18-FLT reflected this dynamic. At 0% serum, uptake of F-18-FLT was heterogeneous but relatively low. At 20% serum, a subpopulation of F-18-FLT-avid cells, representing 61% of the total population, emerged. Uptake of F-18-FLT in this population was 5-fold higher than in the remainder of the cells. Such a dichotomous distribution is not typically observed with other radiotracers, such as F-18-FDG. Conclusion: These results suggest that increased F-18-FLT uptake by proliferating cells is due to a greater fraction of F-18-FLT-avid cells rather than a change in F-18-FLT uptake by individual cells. This finding is consistent with the fact that F-18-FLT uptake is mediated by thymidine kinase 1 expression, which is higher in actively dividing cells. Overall, these findings suggest that, within the same patient, changes in F-18-FLT uptake reflect changes in the number of actively dividing cells, provided other parameters remain the same.
机译:放射性示踪剂3'-脱氧-3'-F-18-氟胸苷(F-18-FLT)通常用于测量体内细胞增殖。作为细胞增殖的标志物,F-18-FLT有望被停滞和活跃分裂的细胞差异吸收,但PET仅能测量肿瘤细胞的聚集摄取,因此F-18-FLT的单细胞分布尚不清楚。我们使用一种新颖的体外放射荧光显微镜技术以单细胞精度测量F-18-FLT放射性示踪剂的差异分布。方法:使用放射荧光显微镜,我们观察了在不同血清条件下生长的MDA-MB-231活细胞中F-18-FLT的绝对摄取。然后,我们使用5-乙炔基-2'-脱氧尿苷掺入固定细胞的荧光显微镜,比较了F-18-FLT摄取与细胞增殖的标准测量值。结果:根据5-乙炔基-2'-脱氧尿苷染色,在缺乏血清的情况下,很少有细胞(1%)活跃地循环,而在不足20%的血清中,大多数细胞(71%)活跃地循环。 F-18-FLT的分布反映了这种动态。血清浓度为0%时,F-18-FLT的摄取不均一,但相对较低。血清浓度为20%时,出现了F-18-FLT-avid细胞亚群,占总人口的61%。该群体中F-18-FLT的摄取比其余细胞高5倍。在其他放射性示踪剂(例如F-18-FDG)中通常不会观察到这种二分分布。结论:这些结果表明,增殖细胞对F-18-FLT摄取的增加是由于F-18-FLT-avid细胞的比例更高,而不是单个细胞对F-18-FLT摄取的改变。这一发现与以下事实相符:F-18-FLT摄取是由胸苷激酶1的表达介导的,在活跃分裂的细胞中这种表达更高。总体而言,这些发现表明,在同一位患者内,只要其他参数保持不变,F-18-FLT摄取的变化将反映活跃分裂细胞数量的变化。

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