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通过与维持干细胞干性和诱导软骨分化相关的分子机制,具有可调硬度的透明质酸水凝胶用于间充质干细胞 3D 培养。

Hyaluronic Acid Hydrogel with Adjustable Stiffness for Mesenchymal Stem Cell 3D Culture via Related Molecular Mechanisms to Maintain Stemness and Induce Cartilage Differentiation.

机构信息

Tianjin Key Laboratory of Biomedical Materials, Institute of Biomedical Engineering, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin 300192, P. R. China.

Fujian Bote Biotechnology Co. Ltd., Fuzhou, Fujian 350013, P. R. China.

出版信息

ACS Appl Bio Mater. 2021 Mar 15;4(3):2601-2613. doi: 10.1021/acsabm.0c01591. Epub 2021 Feb 15.

Abstract

The stemness and differentiation characteristics of bone marrow mesenchymal stem cells (BMSCs) in three-dimensional (3D) culture are of great significance for stem cell therapy and cartilage tissue engineering repair. Moreover, due to their mechanical sensitivity, scaffold materials play important roles in various cell behaviors in 3D culture. In this study, the mechanical strength of hydrogel scaffolds was adjusted by changing the molecular weight of hyaluronic acid (HA). It was proven that BMSCs in a low-strength hydrogel could maintain stemness properties by activating the Wnt/β-catenin pathway for 1 week, while the high-molecular-weight hydrogel with a higher mechanical strength had the potential to promote the direction of cartilage differentiation of BMSCs by opening transient receptor potential vanilloid 4 (TRPV4)/Ca molecular channels, also increasing the expression of type II collagen and SOX9 in BMSCs. This research has a certain reference value for the design of biomaterials for BMSCs' delivery in vivo, as well as the formulation of cartilage repair drug delivery programs based on molecular mechanisms.

摘要

骨髓间充质干细胞(BMSCs)在三维(3D)培养中的干性和分化特性对于干细胞治疗和软骨组织工程修复具有重要意义。此外,由于其对机械刺激敏感,支架材料在 3D 培养中的各种细胞行为中起着重要作用。在这项研究中,通过改变透明质酸(HA)的分子量来调节水凝胶支架的机械强度。研究证明,在低强度水凝胶中,BMSCs 通过激活 Wnt/β-连环蛋白通路 1 周可以维持干性特性,而具有更高机械强度的高分子量水凝胶有潜力通过打开瞬时受体电位香草素 4(TRPV4)/Ca 分子通道来促进 BMSCs 向软骨分化的方向发展,同时也增加了 BMSCs 中 II 型胶原和 SOX9 的表达。这项研究对于设计体内 BMSCs 输送的生物材料以及基于分子机制的软骨修复药物输送方案具有一定的参考价值。

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