Min Jung-Jun, Iyer Meera, Gambhir Sanjiv S
The Crump Institute for Molecular Imaging, Department of Molecular and Medical Pharmacology, UCLA School of Medicine, Los Angeles, CA 90095-1770, USA.
Eur J Nucl Med Mol Imaging. 2003 Nov;30(11):1547-60. doi: 10.1007/s00259-003-1238-6. Epub 2003 Jul 10.
Earlier studies involving comparison of different reporter probes have shown conflicting results between pyrimidine nucleosides [e.g., 2'-fluoro-2'-deoxy-1-beta- d-arabinofuranosyl-5-iodouracil (FIAU)] and acycloguanosine derivatives [e.g., penciclovir (PCV), 9-(4-fluoro-3-hydroxymethylbutyl)guanine (FHBG)]. We hypothesized that this reported discrepancy may be related to how the reporter gene is delivered to the cells-stably transfected vs adenoviral infection. We directly compared the uptake characteristics of [(18)F]FHBG, [(3)H]PCV, and [(14)C]FIAU in cell culture and in vivo using an adenoviral mediated gene transfer model and stably transfected cells. We further compared the uptake of three reporter probes using both HSV1-tk and a mutant HSV1-sr39tk expressing cells to assess the optimal reporter probe/reporter gene combination. [(14)C]FIAU accumulation was greater than that of [(3)H]PCV and [(18)F]FHBG in control cells and in HSV1-tk stably transfected cells ( P<0.001). After infection of C6 cells with AdCMV- HSV1-tk (1.5x10(8) pfu), [(18)F]FHBG and [(3)H]PCV accumulation was significantly greater than that of [(14)C]FIAU ( P<0.01). [(18)F]FHBG and [(3)H]PCV accumulated to a significantly greater extent than [(14)C]FIAU in C6-stb-sr39tk+ and AdCMV- HSV1-sr39tk infected C6 cells ( P<0.001). Results from the nude mice supported the results in cell culture. [(14)C]FIAU led to significantly higher %ID/g in C6-stb-tk+ xenografts than [(18)F]FHBG ( P<0.05); however, compared with [(14)C]FIAU, [(18)F]FHBG led to as high %ID/g in HSV1-tk expressing hepatocytes and to significantly greater %ID/g in C6-stb-sr39tk+ xenografts and HSV1-sr39tk expressing hepatocytes. Dynamic sequential images showed that [(18)F]FHBG was well retained in HSV1-sr39tk expressing cells (C6-stb-sr39tk+) for at least 4 h after injection, while it was rapidly cleared from HSV1-tk expressing cells (MH3924A-stb-tk+). [(14)C]FIAU accumulated in HSV1-tk stably expressing cells to a greater extent than either [(3)H]PCV or [(18)F]FHBG. However, the accumulation of [(3)H]PCV and [(18)F]FHBG in adenoviral infected C6 cells or hepatocytes was equivalent to or greater than that of [(14)C]FIAU. These results may be due to intracellular biochemical changes (e.g., thymidine) when cells are infected with adenovirus. For adenoviral studies, the [(18)F]FHBG/ HSV1-sr39tk combination was shown to be more sensitive than the [(14)C]FIAU/ HSV1-tk combination HSV1-tk.
早期涉及不同报告探针比较的研究表明,嘧啶核苷[如2'-氟-2'-脱氧-1-β-D-阿拉伯呋喃糖基-5-碘尿嘧啶(FIAU)]和无环鸟苷衍生物[如喷昔洛韦(PCV)、9-(4-氟-3-羟甲基丁基)鸟嘌呤(FHBG)]之间的结果相互矛盾。我们推测,报告的这种差异可能与报告基因导入细胞的方式有关——稳定转染与腺病毒感染。我们使用腺病毒介导的基因转移模型和稳定转染的细胞,在细胞培养和体内直接比较了[(18)F]FHBG、[(3)H]PCV和[(14)C]FIAU的摄取特性。我们还使用表达HSV1-tk和突变型HSV1-sr39tk的细胞进一步比较了三种报告探针的摄取情况,以评估最佳的报告探针/报告基因组合。在对照细胞和稳定转染HSV1-tk的细胞中,[(14)C]FIAU的积累量大于[(3)H]PCV和[(18)F]FHBG(P<0.001)。用AdCMV-HSV1-tk(1.5×10(8) 空斑形成单位)感染C6细胞后,[(18)F]FHBG和[(3)H]PCV的积累量显著大于[(14)C]FIAU(P<0.01)。在C6-stb-sr39tk+和AdCMV-HSV1-sr39tk感染的C6细胞中,[(18)F]FHBG和[(3)H]PCV的积累程度显著高于[(14)C]FIAU(P<0.001)。裸鼠实验结果支持了细胞培养实验的结果。[(14)C]FIAU在C6-stb-tk+异种移植瘤中的%ID/g显著高于[(18)F]FHBG(P<0.05);然而,与[(14)C]FIAU相比,[(18)F]FHBG在表达HSV1-tk的肝细胞中的%ID/g与之相当,在C6-stb-sr39tk+异种移植瘤和表达HSV1-sr39tk的肝细胞中的%ID/g显著更高。动态序列图像显示,[(18)F]FHBG在注射后至少4小时内很好地保留在表达HSV1-sr39tk的细胞(C6-stb-sr39tk+)中,而在表达HSV1-tk的细胞(MH3924A-stb-tk+)中迅速清除。[(14)C]FIAU在稳定表达HSV1-tk的细胞中的积累程度大于[(3)H]PCV或[(18)F]FHBG。然而,[(3)H]PCV和[(18)F]FHBG在腺病毒感染的C6细胞或肝细胞中的积累量等于或大于[(14)C]FIAU。这些结果可能是由于细胞感染腺病毒时细胞内的生化变化(如胸苷)所致。对于腺病毒研究,[(18)F]FHBG/HSV1-sr39tk组合比[(14)C]FIAU/HSV1-tk组合更敏感。