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用于骨软骨组织再生的具有双功能单元的原位自组装类器官

In situ self-assembled organoid for osteochondral tissue regeneration with dual functional units.

作者信息

Yang Zhen, Wang Bin, Liu Wei, Li Xiaoke, Liang Kaini, Fan Zejun, Li Jiao Jiao, Niu Yudi, He Zihao, Li Hui, Wang Du, Lin Jianjing, Du Yanan, Lin Jianhao, Xing Dan

机构信息

Arthritis Clinical and Research Center, Peking University People's Hospital, No.11 Xizhimen South Street, Beijing, 100044, China.

Arthritis Institute, Peking University, Beijing, 100044, China.

出版信息

Bioact Mater. 2023 Apr 10;27:200-215. doi: 10.1016/j.bioactmat.2023.04.002. eCollection 2023 Sep.

Abstract

The regeneration of hierarchical osteochondral units is challenging due to difficulties in inducing spatial, directional and controllable differentiation of mesenchymal stem cells (MSCs) into cartilage and bone compartments. Emerging organoid technology offers new opportunities for osteochondral regeneration. In this study, we developed gelatin-based microcryogels customized using hyaluronic acid (HA) and hydroxyapatite (HYP), respectively for inducing cartilage and bone regeneration (denoted as CH-Microcryogels and OS-Microcryogels) through self-assembly into osteochondral organoids. The customized microcryogels showed good cytocompatibility and induced chondrogenic and osteogenic differentiation of MSCs, while also demonstrating the ability to self-assemble into osteochondral organoids with no delamination in the biphasic cartilage-bone structure. Analysis by mRNA-seq showed that CH-Microcryogels promoted chondrogenic differentiation and inhibited inflammation, while OS-Microcryogels facilitated osteogenic differentiation and suppressed the immune response, by regulating specific signaling pathways. Finally, the engraftment of pre-differentiated customized microcryogels into canine osteochondral defects resulted in the spontaneous assembly of an osteochondral unit, inducing simultaneous regeneration of both articular cartilage and subchondral bone. In conclusion, this novel approach for generating self-assembling osteochondral organoids utilizing tailor-made microcryogels presents a highly promising avenue for advancing the field of tissue engineering.

摘要

由于在诱导间充质干细胞(MSCs)向软骨和骨区室进行空间、定向和可控分化方面存在困难,分层骨软骨单元的再生具有挑战性。新兴的类器官技术为骨软骨再生提供了新的机遇。在本研究中,我们分别使用透明质酸(HA)和羟基磷灰石(HYP)定制了基于明胶的微晶凝胶,通过自组装成骨软骨类器官来诱导软骨和骨再生(分别称为CH-微晶凝胶和OS-微晶凝胶)。定制的微晶凝胶显示出良好的细胞相容性,可诱导MSCs的软骨生成和成骨分化,同时还展示了自组装成骨软骨类器官的能力,且在双相软骨-骨结构中无分层现象。mRNA测序分析表明,CH-微晶凝胶通过调节特定信号通路促进软骨生成并抑制炎症,而OS-微晶凝胶则促进成骨分化并抑制免疫反应。最后,将预分化的定制微晶凝胶植入犬骨软骨缺损处,导致骨软骨单元自发组装,诱导关节软骨和软骨下骨同时再生。总之,这种利用定制微晶凝胶生成自组装骨软骨类器官的新方法为推进组织工程领域提供了一条极有前景的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7fd/10121637/64003979a10e/ga1.jpg

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