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人类尿液细胞重编程:合成 3D 肽水凝胶增强诱导多能干细胞群体的均一性。

Human Urinal Cell Reprogramming: Synthetic 3D Peptide Hydrogels Enhance Induced Pluripotent Stem Cell Population Homogeneity.

机构信息

CAS Key Laboratory of Regenerative Biology, Joint School of Life Sciences, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou 510530, China.

Guangzhou Medical University, Guangzhou 511436, China.

出版信息

ACS Biomater Sci Eng. 2020 Nov 9;6(11):6263-6275. doi: 10.1021/acsbiomaterials.0c00667. Epub 2020 Oct 20.

DOI:10.1021/acsbiomaterials.0c00667
PMID:33449655
Abstract

Somatic cells can be reprogrammed into induced pluripotent stem cells (iPSCs), which have promising potential applications in regenerative medicine. However, the challenges of successful applications of human iPSCs for medical purposes are the low generation efficiency, heterogeneous colonies, and exposure to the animal-derived product Matrigel. We aimed to investigate whether human urinal cells could be efficiently reprogrammed into iPSCs in three-dimensional Puramatrix (3D-PM) compared to two-dimensional Matrigel (2D-MG) and to understand how this 3D hydrogel environment affects the reprogramming process. Human urinal cells were successfully reprogrammed into iPSCs in the defined synthetic animal-free 3D-PM. Interestingly, although the colony efficiency in 3D-PM was similar to that in 2D-MG (∼0.05%), the reprogrammed colonies in 3D-PM contained an iPSC population with significantly higher homogeneity, as evidenced by the pluripotent-like morphology and expression of markers. This was further confirmed by transcriptome profile analysis in bulk cells and at the single cell level. Moreover, the homogeneity of the iPSC population in 3D-PM colonies was correlated with the downregulation of integrin β1 (ITGB1) and phosphorylated focal adhesion kinase (FAK). Collectively, 3D-PM provides an alternative approach for obtaining iPSCs with enhanced homogeneity. This work also unveiled the regulation of human somatic cell reprogramming via the extracellular microenvironment.

摘要

体细胞可被重编程为诱导多能干细胞(iPSCs),在再生医学中有很有前景的应用。然而,将人 iPSCs 成功应用于医学的挑战是生成效率低、集落异质性以及接触动物源性产品 Matrigel。我们旨在研究人尿路上皮细胞是否能在三维 Puramatrix(3D-PM)中比二维 Matrigel(2D-MG)更有效地被重编程为 iPSCs,并了解这种 3D 水凝胶环境如何影响重编程过程。人尿路上皮细胞在无动物的定义性合成 3D-PM 中成功被重编程为 iPSCs。有趣的是,尽管 3D-PM 中的集落效率与 2D-MG 相似(约 0.05%),但 3D-PM 中的重编程集落含有具有显著更高均一性的 iPSC 群体,这一点从多能样形态和标志物的表达上得到了证明。这一点在单细胞水平和批量细胞的转录组谱分析中得到了进一步证实。此外,3D-PM 中 iPSC 群体的均一性与整合素 β1(ITGB1)和磷酸化粘着斑激酶(FAK)的下调有关。总之,3D-PM 提供了一种获得均一性增强的 iPSCs 的替代方法。这项工作还揭示了通过细胞外微环境调节人体细胞重编程。

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