Molecular Imaging Program at Stanford, Department of Radiology, 318 Campus Drive, Stanford University, Stanford, California 94305-5427, United States.
ACS Nano. 2012 Jul 24;6(7):5920-30. doi: 10.1021/nn302042y. Epub 2012 Jun 20.
Improved imaging modalities are critically needed for optimizing stem cell therapy. Techniques with real-time content to guide and quantitate cell implantation are especially important in applications such as musculoskeletal regenerative medicine. Here, we report the use of silica-coated gold nanorods as a contrast agent for photoacoustic imaging and quantitation of mesenchymal stem cells in rodent muscle tissue. The silica coating increased the uptake of gold into the cell more than 5-fold, yet no toxicity or proliferation changes were observed in cells loaded with this contrast agent. Pluripotency of the cells was retained, and secretome analysis indicated that only IL-6 was disregulated more than 2-fold from a pool of 26 cytokines. The low background of the technique allowed imaging of down to 100,000 cells in vivo. The spatial resolution is 340 μm, and the temporal resolution is 0.2 s, which is at least an order of magnitude below existing cell imaging approaches. This approach has significant advantages over traditional cell imaging techniques like positron emission tomography and magnetic resonance imaging including real time monitoring of stem cell therapy.
改良的成像模式对于优化干细胞治疗至关重要。具有实时内容以指导和定量细胞植入的技术在肌肉骨骼再生医学等应用中尤为重要。在这里,我们报告了使用硅涂层金纳米棒作为对比剂进行光声成像和定量检测啮齿动物肌肉组织中的间充质干细胞。硅涂层使细胞内金的摄取增加了 5 倍以上,但用这种对比剂加载的细胞没有观察到毒性或增殖变化。细胞的多能性得以保留,分泌组分析表明,在 26 种细胞因子中,只有白细胞介素 6 的调节超过 2 倍。该技术的背景噪音低,可在体内成像低至 100,000 个细胞。空间分辨率为 340μm,时间分辨率为 0.2s,比现有的细胞成像方法至少低一个数量级。与正电子发射断层扫描和磁共振成像等传统细胞成像技术相比,这种方法具有显著优势,包括实时监测干细胞治疗。