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利用人诱导多能干细胞无血清制造间充质干细胞组织环

Serum-Free Manufacturing of Mesenchymal Stem Cell Tissue Rings Using Human-Induced Pluripotent Stem Cells.

作者信息

Winston Tackla S, Suddhapas Kantaphon, Wang Chenyan, Ramos Rafael, Soman Pranav, Ma Zhen

机构信息

Department of Biomedical & Chemical Engineering, Syracuse University, Syracuse NY 13244, USA.

Syracuse Biomaterials Institute, Syracuse University, Syracuse NY 13244, USA.

出版信息

Stem Cells Int. 2019 Jan 15;2019:5654324. doi: 10.1155/2019/5654324. eCollection 2019.

Abstract

Combination of stem cell technology and 3D biofabrication approaches provides physiological similarity to tissues and the capability of repairing and regenerating damaged human tissues. Mesenchymal stem cells (MSCs) have been widely used for regenerative medicine applications because of their immunosuppressive properties and multipotent potentials. To obtain large amount of high-quality MSCs without patient donation and invasive procedures, we differentiated MSCs from human-induced pluripotent stem cells (hiPSC-MSCs) using serum-free E6 media supplemented with only one growth factor (bFGF) and two small molecules (SB431542 and CHIR99021). The differentiated cells showed a high expression of common MSC-specific surface markers (CD90, CD73, CD105, CD106, CD146, and CD166) and a high potency for osteogenic and chondrogenic differentiation. With these cells, we have been able to manufacture MSC tissue rings with high consistency and robustness in pluronic-coated reusable PDMS devices. The MSC tissue rings were characterized based on inner diameter and outer ring diameter and observed cell-type-dependent tissue contraction induced by cell-matrix interaction. Our approach of simplified hiPSC-MSC differentiation, modular fabrication procedure, and serum-free culture conditions has a great potential for scalable manufacturing of MSC tissue rings for different regenerative medicine applications.

摘要

干细胞技术与3D生物制造方法的结合为组织提供了生理相似性以及修复和再生受损人体组织的能力。间充质干细胞(MSCs)因其免疫抑制特性和多能潜力而被广泛用于再生医学应用。为了在无需患者捐赠和侵入性程序的情况下获得大量高质量的间充质干细胞,我们使用仅添加一种生长因子(bFGF)和两种小分子(SB431542和CHIR99021)的无血清E6培养基从人诱导多能干细胞(hiPSC-MSCs)中分化出间充质干细胞。分化后的细胞显示出常见的间充质干细胞特异性表面标志物(CD90、CD73、CD105、CD106、CD146和CD166)的高表达以及成骨和成软骨分化的高效能。利用这些细胞,我们能够在普朗尼克涂层的可重复使用的聚二甲基硅氧烷(PDMS)装置中制造出具有高一致性和稳健性的间充质干细胞组织环。基于内径和外环直径对间充质干细胞组织环进行了表征,并观察到由细胞-基质相互作用诱导的细胞类型依赖性组织收缩。我们简化的hiPSC-MSC分化方法、模块化制造程序和无血清培养条件在为不同再生医学应用可扩展制造间充质干细胞组织环方面具有巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1370/6350554/3c1d8616d28d/SCI2019-5654324.001.jpg

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