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使用纤连蛋白黏附和迁移分析分离软骨细胞和软骨祖细胞。

Isolation of Chondrocytes and Chondroprogenitors using Fibronectin Adhesion and Migratory Assay.

机构信息

Department of Physiology, Christian Medical College; Centre for Stem Cell Research (A unit of InStem, Bengaluru), Christian Medical College;

Centre for Stem Cell Research (A unit of InStem, Bengaluru), Christian Medical College.

出版信息

J Vis Exp. 2024 Oct 4(212). doi: 10.3791/67160.

Abstract

Chondroprogenitor cells (CPCs), recently identified as a distinct subpopulation, exhibit promise due to their mesenchymal properties, heightened chondrogenesis, and limited hypertrophic traits. The enrichment of progenitors is achieved through differential fibronectin adhesion and migration-based explant assays, with Fibronectin Adhesion Assay-derived Chondroprogenitors (FAA-CPs) and Migratory Chondroprogenitors (MCPs) demonstrating superior potential compared to chondrocytes. This article delves into the details of isolating resident cartilage-derived cells, namely chondrocytes and chondroprogenitors. While valuable insights from chondrocyte research contribute to our understanding of cartilage repair, ongoing efforts are directed toward the use of chondroprogenitors and exploring their potential as an alternative therapeutic approach. Additionally, this methodology article provides a detailed step-by-step protocol for isolating three specific cell types from cartilage: chondrocytes, FAA-CPs, and MCPs. By following standardized procedures, this protocol facilitates the successful extraction of these cell subtypes. Grounded in extensive research, the article focuses on the intricate techniques utilized in isolating the different subsets and the optimized culture conditions required to expand and maintain their cultures. The methodology encompasses enzymatic isolation of human articular cartilage-derived chondrocytes, differential fibronectin adhesion following sequential enzymatic digestion, and migration-based explant assays to obtain cartilage-resident cells.

摘要

软骨祖细胞(CPCs)最近被确定为一个独特的亚群,由于其间充质特性、增强的软骨生成能力和有限的肥大特征而备受关注。祖细胞的富集是通过差异纤维连接蛋白黏附和基于迁移的外植体分析来实现的,纤维连接蛋白黏附分析衍生的软骨祖细胞(FAA-CPs)和迁移软骨祖细胞(MCPs)显示出比软骨细胞更好的潜力。本文深入探讨了分离驻留软骨源性细胞(即软骨细胞和软骨祖细胞)的细节。虽然来自软骨细胞研究的宝贵见解有助于我们理解软骨修复,但目前的研究方向是使用软骨祖细胞,并探索它们作为替代治疗方法的潜力。此外,本文提供了一个详细的从软骨中分离三种特定细胞类型(软骨细胞、FAA-CPs 和 MCPs)的分步协议。通过遵循标准化程序,本协议促进了这些细胞亚型的成功提取。本文基于广泛的研究,重点介绍了分离不同亚群所使用的复杂技术以及扩大和维持其培养所需的优化培养条件。该方法包括酶消化分离人关节软骨源性软骨细胞、连续酶消化后的差异纤维连接蛋白黏附和基于迁移的外植体分析,以获得软骨驻留细胞。

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