Institute of Biomaterials & Biomedical Engineering, University of Toronto, Toronto, Canada.
Translational Biology & Engineering Program, Ted Rogers Centre for Heart Research, Toronto, Canada.
Sci Rep. 2018 Aug 14;8(1):12129. doi: 10.1038/s41598-018-30661-w.
MRI for non-invasive cell tracking is recognized for enabling pre-clinical research on stem cell therapy. Yet, adoption of cellular imaging in stem cell research has been restricted to sites with experience in MR contrast agent synthesis and to small animal models that do not require scaled-up synthesis. In this study, we demonstrate the use of a gadolinium-free T1 contrast agent for tracking human embryonic stem cells. The agent, MnPNH, is an easily synthesized manganese porphyrin that can be scaled for large cell numbers. MRI was performed on a 3 T clinical scanner. Cell pellets labeled at different MnPNH concentrations for 24 hours demonstrated a decrease in T1 relaxation time of nearly two-fold (P < 0.05), and cellular contrast was maintained for 24 hours (P < 0.05). Cell viability (Trypan blue) and differentiation (embryoid body formation) were unaffected. Cell uptake of Mn on inductively coupled plasma atomic emission spectroscopy corroborated MRI findings, and fluorescence microscopy revealed the agent localized mainly in cell-cell boundaries and cell nuclei. Labeled cells transplanted in rats demonstrated the superior sensitivity of MnPNH for in-vivo cell tracking.
MRI 用于非侵入性细胞追踪,已被公认为干细胞治疗的临床前研究工具。然而,细胞成像在干细胞研究中的应用仅限于具有 MR 对比剂合成经验的机构,以及不需要大规模合成的小动物模型。在这项研究中,我们展示了一种无钆 T1 对比剂在追踪人胚胎干细胞中的应用。该试剂 MnPNH 是一种易于合成的锰卟啉,可以按大量细胞的数量进行缩放。在 3T 临床扫描仪上进行了 MRI 检查。在 24 小时内用不同 MnPNH 浓度标记的细胞沉淀表明 T1 弛豫时间几乎降低了两倍(P<0.05),并且细胞对比度可维持 24 小时(P<0.05)。细胞活力(台盼蓝)和分化(胚体形成)不受影响。电感耦合等离子体原子发射光谱法的细胞摄取证实了 MRI 的发现,荧光显微镜显示该试剂主要定位于细胞-细胞边界和细胞核。移植到大鼠体内的标记细胞显示出 MnPNH 对体内细胞追踪的优异灵敏度。