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间充质干细胞:分离、表征及体内荧光染料追踪

Mesenchymal stem cells: isolation, characterisation and in vivo fluorescent dye tracking.

作者信息

Weir Christopher, Morel-Kopp Marie-Christine, Gill Anthony, Tinworth Kellie, Ladd Leigh, Hunyor Stephen N, Ward Christopher

机构信息

Cardiac Technology Centre & Kolling Institute, Sydney, Australia.

出版信息

Heart Lung Circ. 2008 Oct;17(5):395-403. doi: 10.1016/j.hlc.2008.01.006.

Abstract

Cell therapies have been used to regenerate the heart by direct myocardial delivery, by coronary infusion and by surface attached scaffolds. Multipotent mesenchymal stem cells (MSC) with capacity to differentiate into cardiomyocytes and other cell lines have been predominantly trialled in rodents. However, large animal models are increasingly needed to translate basic research into new, safe regenerative therapies. Understanding the mode of action of cell therapies in the mammalian heart has been limited by cell tracking capability. This study examined the ability to track the fate of allogeneic MSC in sheep using various fluorescent dyes. MSC isolated from sheep bone marrow were grown in culture following extraction and flow cytometric characterisation. After labelling with fluorescent tracking dyes (e.g. CFSE and DiI) cells were tested for in vitro and in vivo signal up to six weeks. Labelling effect on cell division and differentiation was studied. Several dyes lost fluorescence and slowed cell division. However, the thiol reactive dye CM-DiI showed detectable in vivo fluorescence in labelled MSC six weeks after injection into sheep skeletal muscle and two weeks after implantation of an MSC coated biomaterial scaffold. CM-DiI labelled MSC differentiated in vitro showed label retention over four weeks. The fluorescent membrane dye CM-DiI tracks implanted sheep MSC and provides an alternative to traditional cell markers such as gene modified GFP.

摘要

细胞疗法已被用于通过直接心肌递送、冠状动脉灌注和表面附着支架来使心脏再生。具有分化为心肌细胞和其他细胞系能力的多能间充质干细胞(MSC)主要在啮齿动物中进行了试验。然而,越来越需要大型动物模型将基础研究转化为新的、安全的再生疗法。细胞追踪能力限制了对细胞疗法在哺乳动物心脏中作用方式的理解。本研究使用各种荧光染料检测了追踪绵羊体内异体MSC命运的能力。从绵羊骨髓中分离的MSC在提取和流式细胞术表征后进行培养。在用荧光追踪染料(如CFSE和DiI)标记后,对细胞进行长达六周的体外和体内信号测试。研究了标记对细胞分裂和分化的影响。几种染料失去荧光并减缓细胞分裂。然而,硫醇反应性染料CM-DiI在注射到绵羊骨骼肌六周后以及植入MSC包被的生物材料支架两周后,在标记的MSC中显示出可检测到的体内荧光。体外分化的CM-DiI标记的MSC在四周内保持标记。荧光膜染料CM-DiI可追踪植入的绵羊MSC,并为传统细胞标记物(如基因修饰的GFP)提供了一种替代方法。

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