Suppr超能文献

用于单阶段关节镜下软骨再生治疗的分离人鼻软骨细胞的体外和异位体内研究。

In Vitro and Ectopic In Vivo Studies toward the Utilization of Isolated Human Nasal Chondrocytes for Single-Stage Arthroscopic Cartilage Regeneration Therapy.

机构信息

Department of Orthopaedic Surgery and Traumatology, University Hospital of Basel, 4031 Basel, Switzerland.

Department of Biomedicine, Tissue Engineering Laboratory, University Hospital Basel, University of Basel, 4031 Basel, Switzerland.

出版信息

Int J Mol Sci. 2022 Jun 21;23(13):6900. doi: 10.3390/ijms23136900.

Abstract

Nasal chondrocytes (NCs) have a higher and more reproducible chondrogenic capacity than articular chondrocytes, and the engineered cartilage tissue they generate in vitro has been demonstrated to be safe in clinical applications. Here, we aimed at determining the feasibility for a single-stage application of NCs for cartilage regeneration under minimally invasive settings. In particular, we assessed whether NCs isolated using a short collagenase digestion protocol retain their potential to proliferate and chondro-differentiate within an injectable, swiftly cross-linked and matrix-metalloproteinase (MMP)-degradable polyethylene glycol (PEG) gel enriched with human platelet lysate (hPL). NC-hPL-PEG gels were additionally tested for their capacity to generate cartilage tissue in vivo and to integrate into cartilage/bone compartments of human osteochondral plugs upon ectopic subcutaneous implantation into nude mice. NCs isolated with a protocol and embedded in PEG gels with hPL at low cell density were capable of efficiently proliferating and of generating tissue rich in glycosaminoglycans and collagen II. NC-hPL-PEG gels developed into hyaline-like cartilage tissues upon ectopic in vivo implantation and integrated with surrounding native cartilage and bone tissues. The delivery of NCs in PEG gels containing hPL is a feasible strategy for cartilage repair and now requires further validation in orthotopic in vivo models.

摘要

鼻软骨细胞 (NCs) 的软骨生成能力比关节软骨细胞更高且更具重现性,并且在临床应用中已经证明它们在体外生成的工程化软骨组织是安全的。在这里,我们旨在确定在微创环境下使用 NC 进行单一阶段软骨再生的可行性。特别是,我们评估了使用短胶原酶消化方案分离的 NC 是否能够在富含人血小板裂解物 (hPL) 的可注射、快速交联和基质金属蛋白酶 (MMP) 可降解聚乙二醇 (PEG) 凝胶中增殖和软骨分化。还测试了 NC-hPL-PEG 凝胶在体内生成软骨组织的能力以及在裸鼠异位皮下植入到骨软骨插件的软骨/骨间隙中整合的能力。用方案分离并以低细胞密度嵌入 hPL 的 PEG 凝胶中的 NC 能够有效地增殖并生成富含糖胺聚糖和胶原 II 的组织。NC-hPL-PEG 凝胶在异位体内植入后形成透明样软骨组织,并与周围的天然软骨和骨组织整合。在含有 hPL 的 PEG 凝胶中递送 NC 是一种可行的软骨修复策略,现在需要在原位体内模型中进一步验证。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验