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用于鉴定和研究人类原始多能干细胞的细胞表面标志物。

Cell surface markers for the identification and study of human naive pluripotent stem cells.

作者信息

Trusler Oliver, Huang Ziyi, Goodwin Jacob, Laslett Andrew L

机构信息

CSIRO Manufacturing, Clayton, Victoria 3168, Australia; Australian Regenerative Medicine Institute, Monash University, Victoria 3800, Australia.

CSIRO Manufacturing, Clayton, Victoria 3168, Australia; Australian Regenerative Medicine Institute, Monash University, Victoria 3800, Australia.

出版信息

Stem Cell Res. 2018 Jan;26:36-43. doi: 10.1016/j.scr.2017.11.017. Epub 2017 Dec 2.

Abstract

Characterisation of mouse pluripotent stem cells has revealed two distinct pluripotent states, naive and primed, that maintain characteristics of the pre and post implanted epiblast respectively. Recent studies have developed several culture systems that seek to recapitulate the naive phenomenon in human pluripotent stem cells. Therefore, robust methods to isolate these cells will be fundamental to assess their potential in modelling human development and disease. Here we review current methods for human naive pluripotent culture and collate a list of cell surface antigens that have been identified as markers to differentiate naive from primed human pluripotent stem cells. While these culture systems do display marker variability, and not all antigens mentioned were assessed in all methods, this review provides a resource for researchers of the human naive pluripotent stem cell state. SSEA-4, SSEA-3, CD24, CD75, CD7, CD77, CD130/GP130, CD57, CD90 and NLGN4X were all found to have a +/- expression profile in at least 2 methods, while +/- expression of Tra-1-81, CDH3, CD172a, CD107b, CD229 was reported in one method. Often it was reported that naive and primed cells could be defined using a low/medium/high expression of the following antigens TRA-1-60, PCDH1, GPR64, MHC Class I, however these markers were more likely to display expression pattern differences between methods. Studies using mouse naive cells indicate that they may have benefits over primed cells in modelling development and disease, and while it is yet to be determined if the same can be said about a human naive state, tools to identify this population should greatly further the field.

摘要

对小鼠多能干细胞的表征揭示了两种不同的多能状态,即原始态和始发态,它们分别保持着床前和着床后上胚层的特征。最近的研究开发了几种培养系统,试图在人类多能干细胞中重现原始态现象。因此,强大的分离这些细胞的方法对于评估它们在模拟人类发育和疾病方面的潜力至关重要。在这里,我们回顾了当前人类原始多能培养的方法,并整理了一份已被确定为区分人类原始态和始发态多能干细胞标志物的细胞表面抗原列表。虽然这些培养系统确实显示出标志物的变异性,并且并非所有提到的抗原都在所有方法中进行了评估,但本综述为研究人类原始多能干细胞状态的研究人员提供了一种资源。SSEA-4、SSEA-3、CD24、CD75、CD7、CD77、CD130/GP130、CD57、CD90和NLGN4X在至少两种方法中均呈现出+/-表达模式,而Tra-1-81、CDH3、CD172a、CD107b、CD229的+/-表达在一种方法中有报道。经常有报道称,原始态和始发态细胞可以通过以下抗原的低/中/高表达来定义:TRA-1-60、PCDH1、GPR64、MHC I类,然而这些标志物在不同方法之间更可能表现出表达模式差异。使用小鼠原始态细胞的研究表明,它们在模拟发育和疾病方面可能比始发态细胞更具优势,虽然对于人类原始态是否同样如此尚未确定,但识别这一细胞群体的工具应能极大地推动该领域的发展。

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