Nicholls Francesca J, Rotz Matthew W, Ghuman Harmanvir, MacRenaris Keith W, Meade Thomas J, Modo Michel
Department of Radiology, University of Pittsburgh, PA, USA; McGowan Institute for Regenerative Medicine, University of Pittsburgh, PA, USA; Institute of Psychiatry, Psychology and Neuroscience, King's College London, UK.
Departments of Chemistry, Neurobiology and Radiology, Northwestern University, Evanston, IL, USA; Department of Molecular Biosciences, Northwestern University, Evanston, IL, USA.
Biomaterials. 2016 Jan;77:291-306. doi: 10.1016/j.biomaterials.2015.11.021. Epub 2015 Nov 14.
The unambiguous imaging of transplanted cells remains a major challenge to understand their biological function and therapeutic efficacy. In vivo imaging of implanted cells is reliant on tagging these to differentiate them from host tissue, such as the brain. We here characterize a gold nanoparticle conjugate that is functionalized with modified deoxythymidine oligonucleotides bearing Gd(III) chelates and a red fluorescent Cy3 moiety to visualize in vivo transplanted human neural stem cells. This DNA-Gd@Au nanoparticle (DNA-Gd@AuNP) exhibits an improved T1 relaxivity and excellent cell uptake. No significant effects of cell uptake have been found on essential cell functions. Although T1 relaxivity is attenuated within cells, it is sufficiently preserved to afford the in vivo detection of transplanted cells using an optimized voxel size. In vivo MR images were corroborated by a post-mortem histological verification of DNA-Gd@AuNPs in transplanted cells. With 70% of cells being correctly identified using the DNA-Gd-AuNPs indicates an overall reliable detection. Less than 1% of cells were false positive for DNA-Gd@AuNPs, but a significant number of 30% false negatives reveals a dramatic underestimation of transplanted cells using this approach. DNA-Gd@AuNPs therefore offer new opportunities to visualize transplanted cells unequivocally using T1 contrast and use cellular MRI as a tool to derive biologically relevant information that allows us to understand how the survival and location of implanted cells determines therapeutic efficacy.
对移植细胞进行清晰成像仍然是理解其生物学功能和治疗效果的一项重大挑战。植入细胞的体内成像依赖于对这些细胞进行标记,以便将它们与宿主组织(如大脑)区分开来。我们在此表征了一种金纳米颗粒缀合物,其用带有钆(III)螯合物和红色荧光Cy3部分的修饰脱氧胸苷寡核苷酸进行功能化,以可视化体内移植的人类神经干细胞。这种DNA-Gd@金纳米颗粒(DNA-Gd@AuNP)表现出改善的T1弛豫率和出色的细胞摄取。未发现细胞摄取对基本细胞功能有显著影响。尽管细胞内的T1弛豫率有所衰减,但它仍能充分保留,以便使用优化的体素大小对移植细胞进行体内检测。通过对移植细胞中DNA-Gd@AuNPs进行死后组织学验证,证实了体内磁共振图像。使用DNA-Gd-AuNPs正确识别了70%的细胞,表明总体检测可靠。DNA-Gd@AuNPs的假阳性细胞不到1%,但30%的假阴性细胞数量显著,表明使用这种方法对移植细胞的估计严重不足。因此,DNA-Gd@AuNPs提供了新的机会,利用T1对比清晰地可视化移植细胞,并将细胞磁共振成像用作获取生物学相关信息的工具,使我们能够了解植入细胞的存活和位置如何决定治疗效果。