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水凝胶内培养防止了单层扩增诱导的间充质干细胞的转化。

Intra-hydrogel culture prevents transformation of mesenchymal stem cells induced by monolayer expansion.

机构信息

Guangxi Engineering Center in Biomedical Materials for Tissue and Organ Regeneration, Guangxi Collaborative Innovation Center for Biomedicine, The First Affiliated Hospital of Guangxi Medical University, 530021, Nanning, China.

Department of Orthopaedics Trauma and Hand Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.

出版信息

Biomater Sci. 2018 May 1;6(5):1168-1176. doi: 10.1039/C8BM00007G.

Abstract

In this study, we report that the intra-hydrogel culture system mitigates the transformation of mesenchymal stem cells (MSCs) induced by two-dimensional (2D) expansion. MSCs expanded in monolayer culture prior to encapsulation in collagen hydrogels (group eMSCs-CH) featured impaired stemness in chondrogenesis, comparing with the freshly isolated bone marrow mononuclear cells seeded directly in collagen hydrogels (group fMSCs-CH). The molecular mechanism of the in vitro expansion-triggered damage to MSCs was detected through genome-wide microarray analysis. Results indicated that pathways such as proteoglycans in cancer and pathways in cancer expansion were highly enriched in eMSCs-CH. And multiple up-regulated oncoma-associated genes were verified in eMSCs-CH compared with fMSCs-CH, indicating that expansion in vitro triggered cellular transformation was associated with signaling pathways related to tumorigenicity. Besides, focal adhesion (FA) and mitogen-activated protein kinase (MAPK) signaling pathways were also involved in in vitro expansion, indicating restructuring of the cell architecture. Thus, monolayer expansion in vitro may contribute to vulnerability of MSCs through the regulation of FA and MAPK. This study indicates that intra-hydrogel culture can mitigate the monolayer expansion induced transformation of MSCs and maintain the uniformity of the stem cells, which is a viable in vitro culture system for stem cell therapy.

摘要

在这项研究中,我们报告称,水凝胶内培养系统减轻了二维(2D)扩增诱导的间充质干细胞(MSCs)的转化。与直接接种在胶原水凝胶中的新鲜分离的骨髓单核细胞(fMSCs-CH 组)相比,在胶原水凝胶中包封之前在单层培养中扩增的 MSCs 在软骨生成中表现出干细胞特性受损。通过全基因组微阵列分析检测体外扩增对 MSCs 造成损伤的分子机制。结果表明,在 eMSCs-CH 中,癌症中的蛋白聚糖和癌症扩增途径等途径高度富集。与 fMSCs-CH 相比,eMSCs-CH 中多个上调的癌相关基因得到验证,表明体外扩增引发的细胞转化与与致瘤性相关的信号通路有关。此外,黏着斑(FA)和丝裂原活化蛋白激酶(MAPK)信号通路也参与了体外扩增,表明细胞结构的重构。因此,体外单层扩增可能通过调节 FA 和 MAPK 导致 MSCs 的脆弱性。这项研究表明,水凝胶内培养可以减轻 MSCs 单层扩增诱导的转化,并保持干细胞的均一性,这是一种可行的干细胞治疗体外培养系统。

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