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骨软骨缺损的修复:含人骨髓间充质干细胞和人诱导多能干细胞软骨颗粒的组织工程混合植入物的疗效

Repair of osteochondral defects: efficacy of a tissue-engineered hybrid implant containing both human MSC and human iPSC-cartilaginous particles.

作者信息

Nakagawa Shinichi, Ando Wataru, Shimomura Kazunori, Hart David A, Hanai Hiroto, Jacob George, Chijimatsu Ryota, Yarimitu Seido, Fujie Hiromichi, Okada Seiji, Tsumaki Noriyuki, Nakamura Norimasa

机构信息

Department of Orthopaedic Surgery, Osaka University Graduate School of Medicine, Suita, 565-0871, Japan.

Department of Orthopaedic Surgery, Kansai Rosai Hospital, Amagasaki, 660-8511, Japan.

出版信息

NPJ Regen Med. 2023 Oct 19;8(1):59. doi: 10.1038/s41536-023-00335-x.

Abstract

Both mesenchymal stromal cells (MSC) and induced pluripotent stem cells (iPSC) offer the potential for repair of damaged connective tissues. The use of hybrid implants containing both human MSC and iPSC was investigated to assess their combined potential to yield enhanced repair of osteochondral defects. Human iPSC-CP wrapped with tissue engineered constructs (TEC) containing human MSC attained secure defect filling with good integration to adjacent tissue in a rat osteochondral injury model. The presence of living MSC in the hybrid implants was required for effective biphasic osteochondral repair. Thus, the TEC component of such hybrid implants serves several critical functions including, adhesion to the defect site via the matrix and facilitation of the repair via live MSC, as well as enhanced angiogenesis and neovascularization. Based on these encouraging studies, such hybrid implants may offer an effective future intervention for repair of complex osteochondral defects.

摘要

间充质基质细胞(MSC)和诱导多能干细胞(iPSC)都具有修复受损结缔组织的潜力。研究了使用包含人类MSC和iPSC的混合植入物,以评估它们联合修复骨软骨缺损的增强潜力。在大鼠骨软骨损伤模型中,用人MSC包裹的组织工程构建体(TEC)包裹的人类iPSC-CP实现了安全的缺损填充,并与相邻组织良好整合。混合植入物中活的MSC的存在是有效的双相骨软骨修复所必需的。因此,这种混合植入物的TEC成分具有几个关键功能,包括通过基质与缺损部位粘附、通过活的MSC促进修复,以及增强血管生成和新生血管形成。基于这些令人鼓舞的研究,这种混合植入物可能为复杂骨软骨缺损的修复提供一种有效的未来干预措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a0c/10587071/889b15602ad0/41536_2023_335_Fig1_HTML.jpg

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