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用吲哚菁绿标记人胚胎干细胞来源的心肌细胞,用于光学成像的非侵入性追踪:一种与萤火虫荧光素酶兼容的 FDA 替代方法。

Labeling human embryonic stem cell-derived cardiomyocytes with indocyanine green for noninvasive tracking with optical imaging: an FDA-compatible alternative to firefly luciferase.

机构信息

Department of Radiology, University of California, San Francisco, CA 94107-0946, USA.

出版信息

Cell Transplant. 2010;19(1):55-65. doi: 10.3727/096368909X478579.

Abstract

Human embryonic stem cell-derived cardiomyocytes (hESC-CMs) have demonstrated the ability to improve myocardial function following transplantation into an ischemic heart; however, the functional benefits are transient possibly due to poor cell retention. A diagnostic technique that could visualize transplanted hESC-CMs could help to optimize stem cell delivery techniques. Thus, the purpose of this study was to develop a labeling technique for hESCs and hESC-CMs with the FDA-approved contrast agent indocyanine green (ICG) for optical imaging (OI). hESCs were labeled with 0.5, 1.0, 2.0, and 2.5 mg/ml of ICG for 30, 45, and 60 min at 37 degrees C. Longitudinal OI studies were performed with both hESCs and hESC-CMs. The expression of surface proteins was assessed with immunofluorescent staining. hESCs labeled with 2 mg ICG/ml for 60 min achieved maximum fluorescence. Longitudinal studies revealed that the fluorescent signal was equivalent to controls at 120 h postlabeling. The fluorescence signal of hESCs and hESC-CMs at 1, 24, and 48 h was significantly higher compared to precontrast data (p < 0.05). Immunocytochemistry revealed retention of cell-specific surface and nuclear markers postlabeling. These data demonstrate that hESCs and hESC-CMs labeled with ICG show a significant fluorescence up to 48 h and can be visualized with OI. The labeling procedure does not impair the viability or functional integrity of the cells. The technique may be useful for assessing different delivery routes in order to improve the engraftment of transplanted hESC-CMs or other stem cell progenitors.

摘要

人胚胎干细胞衍生的心肌细胞(hESC-CMs)在移植到缺血性心脏后显示出改善心肌功能的能力;然而,由于细胞保留率差,其功能益处是短暂的。一种可以可视化移植的 hESC-CMs 的诊断技术可以帮助优化干细胞递送技术。因此,本研究的目的是开发一种用 FDA 批准的对比剂吲哚菁绿(ICG)对 hESC 和 hESC-CMs 进行光学成像(OI)的标记技术。hESC 用 0.5、1.0、2.0 和 2.5 mg/ml 的 ICG 在 37°C 下标记 30、45 和 60 分钟。对 hESC 和 hESC-CMs 进行了纵向 OI 研究。用免疫荧光染色评估表面蛋白的表达。hESC 用 2 mg/ml 的 ICG 标记 60 分钟可获得最大荧光。纵向研究表明,标记后 120 小时荧光信号与对照相当。hESC 和 hESC-CMs 在 1、24 和 48 小时的荧光信号明显高于对照数据(p < 0.05)。免疫细胞化学显示标记后细胞特异性表面和核标记物的保留。这些数据表明,用 ICG 标记的 hESC 和 hESC-CMs 可在 48 小时内显示出显著的荧光,并可通过 OI 可视化。标记过程不会损害细胞的活力或功能完整性。该技术可用于评估不同的输送途径,以改善移植的 hESC-CMs 或其他干细胞祖细胞的植入。

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