Molecular and Preclinical Imaging Centers, Department of Molecular Biotechnology and Health Sciences, University of Turin, Torino, Italy.
Department of Molecular Biotechnology and Health Sciences, University of Turin, Torino, Italy.
J Biophotonics. 2019 May;12(5):e201800035. doi: 10.1002/jbio.201800035. Epub 2019 Feb 1.
The transplantation of mesenchymal stem cells (MSCs) holds great promise for the treatment of a plethora of human diseases, but new noninvasive procedures are needed to monitor the cell fate in vivo. Already largely used in medical diagnostics, the fluorescent dye indocyanine green (ICG) is an established dye to track limited numbers of cells by optical imaging (OI), but it can also be visualized by photoacoustic imaging (PAI), which provides a higher spatial resolution than pure near infrared fluorescence imaging (NIRF). Because of its successful use in clinical and preclinical examinations, we chose ICG as PAI cell labeling agent. Optimal incubation conditions were defined for an efficient and clinically translatable MSC labeling protocol, such that no cytotoxicity or alterations of the phenotypic profile were observed, and a consistent intracellular uptake of the molecule was achieved. Suspensions of ICG-labeled cells were both optically and optoacoustically detected in vitro, revealing a certain variability in the photoacoustic spectra acquired by varying the excitation wavelength from 680 to 970 nm. Intramuscular engraftments of ICG-labeled MSCs were clearly visualized by both PAI and NIRF over few days after transplantation in the hindlimb of healthy mice, suggesting that the proposed technique retains a considerable potential in the field of transplantation-focused research and therapy. Stem cells were labeled with the Food and Drug Administration (FDA)-approved fluorescent dye ICG, and detected by both PAI and OI, enabling to monitor the cell fate safely, in dual modality, and with good sensitivity and improved spatial resolution.
间充质干细胞 (MSCs) 的移植在治疗多种人类疾病方面具有广阔的前景,但需要新的非侵入性程序来监测体内细胞的命运。荧光染料吲哚菁绿 (ICG) 已广泛用于医学诊断,是通过光学成像 (OI) 追踪有限数量细胞的成熟染料,但也可以通过光声成像 (PAI) 可视化,PAI 比纯近红外荧光成像 (NIRF) 具有更高的空间分辨率。由于其在临床和临床前检查中的成功应用,我们选择 ICG 作为 PAI 细胞标记剂。定义了最佳孵育条件,以制定一种高效且可临床转化的 MSC 标记方案,即观察到没有细胞毒性或表型特征改变,并且实现了分子的一致细胞内摄取。ICG 标记细胞的悬浮液在体外通过光学和光声都可检测到,表明通过将激发波长从 680nm 变化到 970nm 来获得的光声光谱存在一定的可变性。在健康小鼠后肢中,将 ICG 标记的 MSC 进行肌内移植后几天,通过 PAI 和 NIRF 均可以清晰地观察到 ICG 标记的 MSC,这表明该技术在移植为重点的研究和治疗领域仍具有相当大的潜力。干细胞用食品和药物管理局 (FDA) 批准的荧光染料 ICG 标记,并通过 PAI 和 OI 检测,能够以良好的灵敏度和提高的空间分辨率安全地以双模态监测细胞命运。