Moore A, Basilion J P, Chiocca E A, Weissleder R
Center for Molecular Imaging Research, Massachusetts General Hospital, Harvard Medical School, Charlestown 02129, USA.
Biochim Biophys Acta. 1998 Apr 24;1402(3):239-49. doi: 10.1016/s0167-4889(98)00002-0.
The human transferrin receptor (hTfR) has been used as a model molecular target to direct therapeutic agents to tumor cells and to shuttle drugs across the blood-brain-barrier. We show in the current study that receptor expression and regulation can be visualized by NMR imaging, when the receptor is probed with a sterically protected iron containing magnetic hTfR probe. We were able to demonstrate that the novel receptor probe was an iron source that could enter the cells via the hTfR but did not play an immediate role in iron downregulation of hTfR within incubation times tested. Using genetically engineered rat 9L gliosarcoma cell lines with three different forms of the hTfR, we also demonstrated that receptor expression and regulation can be visualized by NMR imaging using the probe. This research provides proof of the principle that it is possible to image receptor gene expression and regulation and it demonstrates that it may be possible to image gene transfer in vivo.
人转铁蛋白受体(hTfR)已被用作一个模型分子靶点,用于将治疗药物导向肿瘤细胞并使药物穿过血脑屏障。我们在当前研究中表明,当用一种空间位阻保护的含铁血hTfR探针探测该受体时,可通过核磁共振成像观察到受体的表达和调控情况。我们能够证明这种新型受体探针是一种铁源,它可以通过hTfR进入细胞,但在所测试的孵育时间内,它在hTfR的铁下调过程中没有立即发挥作用。利用具有三种不同形式hTfR的基因工程大鼠9L胶质肉瘤细胞系,我们还证明了使用该探针通过核磁共振成像可以观察到受体的表达和调控情况。这项研究提供了原理证明,即有可能对受体基因的表达和调控进行成像,并且表明有可能在体内对基因转移进行成像。