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一种用于血管内皮细胞和骨髓间充质干细胞共培养的可注射双网络水凝胶,可同时增强血管生成和成骨作用。

An injectable double-network hydrogel for the co-culture of vascular endothelial cells and bone marrow mesenchymal stem cells for simultaneously enhancing vascularization and osteogenesis.

作者信息

Yang Congchong, Han Bing, Cao Chunling, Yang Di, Qu Xiaozhong, Wang Xiaoyan

机构信息

Department of Cariology and Endodontology, National Engineering Laboratory for Digital and Material Technology of Stomatology, Peking Key Laboratory of Digital Stomatology, Peking University School and Hospital of Stomatology, Beijing 100081, China.

出版信息

J Mater Chem B. 2018 Dec 21;6(47):7811-7821. doi: 10.1039/c8tb02244e. Epub 2018 Oct 22.

Abstract

The achievement of rapid vascularization in large implanted constructs is a major challenge in the field of bone tissue engineering. Although co-culture of bone-forming cells and vascular endothelial cells (VECs) has been expected to be a way of promoting vascularization during bone formation with a scaffold, there is a lack of detailed knowledge about the direct interactions between two types of stem cells in a three-dimensional (3D) extracellular matrix (ECM). Herein, we report on the use of an injectable cytocompatible double-network (DN) hydrogel to encapsulate, co-culture and subsequently stimulate the angiogenic/osteogenic differentiation of VECs and the human bone marrow mesenchymal stem cells (BM-MSCs), which demonstrates that the direct co-cultured system enables simultaneous enhancement of vascularization and osteogenesis by providing 3D cell-cell communication. Besides, the improved mechanical properties and the injectability of the DN hydrogel allow the delivery, long-time implantation, proliferation and differentiation of stem cells in vivo. Therefore, this study could provide a niche-like native ECM for stem cell survival and the regulation of the differentiation of multiple cell lines which will benefit bone repair.

摘要

在大型植入物构建体中实现快速血管化是骨组织工程领域的一项重大挑战。尽管成骨细胞与血管内皮细胞(VECs)共培养有望成为在支架辅助骨形成过程中促进血管化的一种方法,但对于两种类型的干细胞在三维(3D)细胞外基质(ECM)中的直接相互作用,仍缺乏详细了解。在此,我们报道了使用一种可注射的细胞相容性双网络(DN)水凝胶来包裹、共培养并随后刺激VECs和人骨髓间充质干细胞(BM-MSCs)的血管生成/成骨分化,这表明直接共培养系统通过提供3D细胞间通讯能够同时增强血管化和成骨作用。此外,DN水凝胶改善的机械性能和可注射性允许干细胞在体内递送、长期植入、增殖和分化。因此,本研究可为干细胞存活及多种细胞系分化调控提供类似小生境的天然ECM,这将有利于骨修复。

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