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脱细胞化全骨软骨片生物支架可促进兔模型中负载间充质干细胞的增殖和分化。

A bioscaffold of decellularized whole osteochondral sheet improves proliferation and differentiation of loaded mesenchymal stem cells in a rabbit model.

机构信息

Department of Stem Cells and Developmental Biology, Cell Science Research Centre, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.

Department of Developmental Biology, University of Science and Culture, Tehran, Iran.

出版信息

Cell Tissue Bank. 2023 Dec;24(4):711-724. doi: 10.1007/s10561-023-10084-2. Epub 2023 Mar 20.

Abstract

As a Natural decellularized extracellular matrix, osteochondral tissue is the best scaffold for the restoration of osteoarthritis defects. Bioscaffolds have the most similarly innate properties like biomechanical properties and the preserved connection of the bone-to-cartilage border. Although, their compacity and low porosity particularly, are proven to be difficulties of decellularization and cell penetration. This study aims to develop a new bioscaffold of decellularized osteochondral tissue (DOT) that is recellularized by bone marrow-derived mesenchymal stem cells (BM-MSCs), as a biphasic allograft, which preserved the interface between the cartilage section and subchondral bone of the joint. Whole osteochondral tissues of rabbit knee joints were sheeted in cartilaginous parts in 200-250 µm sections while connected to the subchondral bone and then fully decellularized. The BM-MSCs were seeded on the scaffolds in vitro; some constructs were subcutaneously implanted into the back of the rabbit. The cell penetration, differentiation to bone and cartilage, viability, and cell proliferation in vitro and in vivo were evaluated by qPCR, histological staining, MTT assay, and immunohistochemistry. DNA content analysis and SEM assessments confirmed the decellularization of the bioscaffold. Then, histological and SEM evaluations indicated that the cells could successfully penetrate the bone and cartilage lacunas in implanted grafts. MTT assay confirmed cell proliferation. Prominently, gene expression analysis showed that seeded cells differentiated into osteoblasts and chondrocytes in both bone and cartilage sections. More importantly, seeded cells on the bioscaffold started ECM secretion. Our results indicate that cartilage-to-bone border integrity was largely preserved. Additionally, ECM-sheeted DOT could be employed as a useful scaffold for promoting the regeneration of osteochondral defects.

摘要

作为一种天然去细胞细胞外基质,软骨组织是修复骨关节炎缺损的最佳支架。生物支架具有最相似的内在特性,如生物力学特性和骨软骨交界处的保留连接。然而,其致密性和低孔隙率,特别是被证明是去细胞化和细胞渗透的困难。本研究旨在开发一种新的去细胞化软骨组织(DOT)生物支架,该支架由骨髓间充质干细胞(BM-MSCs)再细胞化,作为双相同种异体移植物,保留了关节软骨部分和软骨下骨之间的界面。兔膝关节的整个软骨组织在软骨部分以 200-250µm 的切片成片状,同时与软骨下骨相连,然后完全去细胞化。BM-MSCs 在体外接种在支架上;一些构建物被皮下植入兔的背部。通过 qPCR、组织学染色、MTT 测定和免疫组织化学评估细胞渗透、向骨和软骨的分化、体外和体内的活力和细胞增殖。DNA 含量分析和 SEM 评估证实了生物支架的去细胞化。然后,组织学和 SEM 评估表明,细胞可以成功地穿透植入移植物中的骨和软骨腔隙。MTT 测定证实了细胞增殖。突出的是,基因表达分析表明,接种的细胞在骨和软骨部分分化为成骨细胞和软骨细胞。更重要的是,在生物支架上接种的细胞开始分泌细胞外基质。我们的结果表明,软骨-骨边界的完整性得到了很大的保留。此外,ECM 片状 DOT 可作为促进骨软骨缺损再生的有用支架。

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