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用于体外纯化和体内追踪人多能干细胞来源肝细胞的合成探针。

Synthetic probes for in vitro purification and in vivo tracking of hepatocytes derived from human pluripotent stem cells.

机构信息

Laboratory of Stem Cells and Tissue Regeneration, Department of Biotechnology, College of Life Sciences and Biotechnology, Korea University, Seoul, 02841, South Korea.

Department of Biological Sciences, Hyupsung University, Hwasung-si, 18330, South Korea.

出版信息

Biomaterials. 2019 Nov;222:119431. doi: 10.1016/j.biomaterials.2019.119431. Epub 2019 Aug 14.

Abstract

Hepatocytes derived from human pluripotent stem cells (hPSCs) are promising candidates for cell therapy and drug discovery. However, it remains challenging to efficiently purify hepatocytes from undesired cell types after differentiation and to accurately monitor grafted cells after transplantation. Indocyanine Green (ICG), an FDA-approved, near-infrared (NIR) dye, has been used for various clinical purposes and is exclusively taken up by hepatocytes. However, ICG has a long emission wavelength (λ > 800 nm) that is beyond the detection range of fluorescence-activated cell sorting (FACS) systems. Moreover, it is easily eliminated from hepatocytes, hindering its application for NIR imaging. Here, we designed and synthesized two different probes based on the properties of ICG; 1) hepatocyte purifying agent (HPA, λ = 562 nm) for in vitro sorting and 2) hepatocyte imaging agent (HIA, λ = 817 nm) for efficient in vivo NIR imaging. We obtained highly enriched populations of hPSC-derived hepatocytes (hPSC-Heps) from various hPSC lines using HPA probe-based FACS purification. In addition, HIA labelling and NIR imaging allowed the direct visualization and tracking of grafted hPSC-Heps in animals with liver injuries. These results demonstrated that these two probes could be used as powerful tools with hPSC-Heps in both cell replacement therapy and drug screening.

摘要

人多能干细胞(hPSCs)衍生的肝细胞是细胞治疗和药物发现的有前途的候选物。然而,从分化后的非期望细胞类型中高效地纯化肝细胞,以及在移植后准确监测移植细胞仍然具有挑战性。吲哚菁绿(ICG)是一种获得 FDA 批准的近红外(NIR)染料,已被用于各种临床用途,并且仅被肝细胞摄取。然而,ICG 的发射波长较长(λ>800nm),超出了荧光激活细胞分选(FACS)系统的检测范围。此外,它很容易从肝细胞中消除,这阻碍了其在近红外成像中的应用。在这里,我们根据 ICG 的特性设计并合成了两种不同的探针;1)用于体外分选的肝细胞纯化剂(HPA,λ=562nm)和 2)用于高效体内 NIR 成像的肝细胞成像剂(HIA,λ=817nm)。我们使用基于 HPA 探针的 FACS 纯化从各种 hPSC 系中获得了高度富集的 hPSC 衍生的肝细胞(hPSC-Heps)群体。此外,HIA 标记和 NIR 成像允许在具有肝损伤的动物中直接可视化和跟踪移植的 hPSC-Heps。这些结果表明,这两种探针可以作为在细胞替代治疗和药物筛选中使用 hPSC-Heps 的有力工具。

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