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从角质形成细胞衍生的人诱导多能干细胞生成功能性血管内皮细胞和平滑肌周细胞。

Generation of Functional Vascular Endothelial Cells and Pericytes from Keratinocyte Derived Human Induced Pluripotent Stem Cells.

作者信息

Pars Selin, Achberger Kevin, Kleger Alexander, Liebau Stefan, Pashkovskaia Natalia

机构信息

Institute of Neuroanatomy & Developmental Biology (INDB), Eberhard Karls University Tübingen, Österbergstrasse 3, 72074 Tübingen, Germany.

Department of Internal Medicine 1, Ulm University Hospital, 89081 Ulm, Germany.

出版信息

Cells. 2021 Jan 5;10(1):74. doi: 10.3390/cells10010074.

Abstract

Human induced pluripotent stem cell (hiPSC)-derived endothelial cells (ECs) and pericytes provide a powerful tool for cardiovascular disease modelling, personalized drug testing, translational medicine, and tissue engineering. Here, we report a novel differentiation protocol that results in the fast and efficient production of ECs and pericytes from keratinocyte-derived hiPSCs. We found that the implementation of a 3D embryoid body (EB) stage significantly improves the differentiation efficiency. Compared with the monolayer-based technique, our protocol yields a distinct EC population with higher levels of EC marker expression such as CD31 and vascular endothelial cadherin (VE-cadherin). Furthermore, the EB-based protocol allows the generation of functional EC and pericyte populations that can promote blood vessel-like structure formation upon co-culturing. Moreover, we demonstrate that the EB-based ECs and pericytes can be successfully used in a microfluidic chip model, forming a stable 3D microvascular network. Overall, the described protocol can be used to efficiently differentiate both ECs and pericytes with distinct and high marker expression from keratinocyte-derived hiPSCs, providing a potent source material for future cardiovascular disease studies.

摘要

人诱导多能干细胞(hiPSC)来源的内皮细胞(ECs)和平滑肌细胞为心血管疾病建模、个性化药物测试、转化医学和组织工程提供了一个强大的工具。在此,我们报告了一种新的分化方案,该方案可从角质形成细胞来源的hiPSC快速高效地生成ECs和平滑肌细胞。我们发现实施三维胚状体(EB)阶段可显著提高分化效率。与基于单层的技术相比,我们的方案产生了一个独特的EC群体,其EC标志物如CD31和血管内皮钙黏蛋白(VE-钙黏蛋白)的表达水平更高。此外,基于EB的方案允许生成功能性的EC和平滑肌细胞群体,在共培养时可促进血管样结构的形成。此外,我们证明基于EB的ECs和平滑肌细胞可成功用于微流控芯片模型,形成稳定的三维微血管网络。总体而言,所描述的方案可用于从角质形成细胞来源的hiPSC高效分化出具有独特且高标志物表达的ECs和平滑肌细胞,为未来心血管疾病研究提供了一种有力的源材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c090/7824831/07ed96bd356f/cells-10-00074-g001.jpg

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