小鼠原代软骨细胞的体外分离培养及软骨生物学研究。

IF 1.2 4区 综合性期刊 Q3 MULTIDISCIPLINARY SCIENCES
Qingxin Song, Yangwei Xu, Yajie Xie, Xinyu Huo, Jian Sun, Yitong Zhao, Wenfang Wang
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引用次数: 0

摘要

关节软骨破坏导致软骨细胞活性改变,这是多种软骨疾病的主要致病因素,包括骨关节炎(OA)和类风湿性关节炎(RA)。作为软骨中最丰富的细胞类型,深入研究软骨细胞的生物学特性对于制定有效的疾病治疗策略至关重要。原代软骨细胞的分离和培养为研究软骨疾病提供了重要的实验材料,有助于揭示软骨损伤和修复的机制。本方案提供了小鼠原代软骨细胞的体外分离和培养方法的详细描述。采用优化后的胶原酶II方案,新生小鼠膝关节软骨标本的软骨细胞分离可在8 h内完成。细胞产量约为1-2 × 10³细胞/mg软骨组织,随组织新鲜度和初始细胞密度的变化而变化;分离的细胞存活率为90%。本方案以小鼠原代软骨细胞为例,显示分离后1、2、5天细胞的形态特征和粘附状态。逆转录定量聚合酶链反应(RT-qPCR)和western blotting结果显示,白细胞介素-1β (IL-1β)处理降低了胶原型α 1 (Col2a1),增加了基质金属肽酶13 (Mmp13)的表达,证实了分离的软骨细胞对炎症刺激有反应。与传统方法相比,该方案采用更高的胶原酶浓度,以减少延长分离时间对细胞活力的影响,同时避免胰蛋白酶处理对细胞的潜在损伤。获得的原代软骨细胞纯度高、活力好,适合深入研究软骨损伤相关机制,对软骨疾病的体外研究和临床治疗具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In vitro Isolation and Culturing of Mouse Primary Chondrocytes for Cartilage Biology.

Articular cartilage destruction leads to altered chondrocyte activity, which is a major causative factor in a variety of cartilage diseases, including osteoarthritis (OA) and rheumatoid arthritis (RA). As the most abundant cell type in cartilage, an in-depth study of the biological properties of chondrocytes is essential for the development of effective disease treatment strategies. Isolation and culturing of primary chondrocytes provide important experimental materials for the investigation of cartilage disease and contribute to unraveling the mechanisms of cartilage injury and repair. This protocol provides a detailed description of the in vitro isolation and culturing methods for primary chondrocytes derived from mice. By using the optimized collagenase II protocol, chondrocyte isolation can be completed within 8 h for neonatal mouse knee joint cartilage specimens. The cell yield is approximately 1-2 × 10³ cells/mg of cartilage tissue, varying with tissue freshness and initial cell density; the isolated cells exhibit >90% viability. This protocol uses mouse primary chondrocytes as an example, showing the morphological characteristics and adhesion status of cells cultured for 1, 2, and 5 days after isolation. Reverse transcription quantitative polymerase chain reaction (RT-qPCR) and western blotting showed that interleukin-1β (IL-1β) treatment reduced Collagen Type II Alpha 1 (Col2a1) and increased Matrix Metallopeptidase 13 (Mmp13) expression, confirming that isolated chondrocytes respond to inflammatory stimuli. Compared with conventional methods, this protocol employs a higher collagenase concentration to reduce the impact of prolonged isolation time on cell viability, while avoiding potential cell damage from trypsin treatment. The obtained primary chondrocytes are pure and viable, suitable for in-depth studies on cartilage injury-related mechanisms, which have important implications for in vitro research and the clinical treatment of cartilage disease.

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来源期刊
Jove-Journal of Visualized Experiments
Jove-Journal of Visualized Experiments MULTIDISCIPLINARY SCIENCES-
CiteScore
2.10
自引率
0.00%
发文量
992
期刊介绍: JoVE, the Journal of Visualized Experiments, is the world''s first peer reviewed scientific video journal. Established in 2006, JoVE is devoted to publishing scientific research in a visual format to help researchers overcome two of the biggest challenges facing the scientific research community today; poor reproducibility and the time and labor intensive nature of learning new experimental techniques.
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