Department of Anatomy, Histology, and Embryology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Genomic Medicine and Bioinformatic Core Facility, Department of Biochemistry and Molecular Biology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Curr Protoc. 2023 Mar;3(3):e692. doi: 10.1002/cpz1.692.
Articular cartilage is characterized by a low density of chondrocytes surrounded by an abundant extracellular matrix (ECM) consisting of a dense mixture of collagens, proteoglycans, and glycosaminoglycans. Due to its low cellularity and high proteoglycan content, it is particularly challenging to extract high-quality total RNA suitable for sensitive high-throughput downstream applications such as RNA sequencing (RNA-Seq). Available protocols for high-quality RNA isolation from articular chondrocytes are inconsistent, resulting in suboptimal yield and compromised quality. This poses a significant difficulty in the application of RNA-Seq to study the cartilage transcriptome. Current protocols rely either on dissociation of cartilage ECM by collagenase digestion or pulverizing cartilage using various methods prior to RNA extraction. However, protocols for cartilage processing vary significantly depending on the species and source of cartilage within the body. Protocols for isolating RNA from human or large mammal (e.g., horse or cattle) cartilage samples are available, but this is not the case for chicken cartilage, despite the species being extensively used in cartilage research. Here, we present two improved RNA isolation protocols based on pulverization of fresh articular cartilage using a cryogenic mill or on enzymatic digestion using 1.2% (w/v) collagenase II. Our protocols optimize the collection and tissue processing steps to minimize RNA degradation and enhance RNA purity. Our results show that RNA purified from chicken articular cartilage using these methods has appropriate quality for RNA-Seq experiments. The procedure is applicable for RNA extraction from cartilage from other species such as dog, cat, sheep, and goat. The workflow for RNA-Seq analysis is also described here. © 2023 The Authors. Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: Extraction of total RNA from pulverized chicken articular cartilage Alternate Protocol: Extraction of total RNA from collagen-digested articular cartilage Support Protocol: Dissection of chicken articular cartilage from the knee joint Basic Protocol 2: RNA sequencing of total RNA from chicken articular cartilage.
关节软骨的特征是软骨细胞密度低,周围是丰富的细胞外基质(ECM),由胶原、蛋白聚糖和糖胺聚糖的致密混合物组成。由于其细胞密度低和蛋白聚糖含量高,因此特别难以提取适合敏感高通量下游应用(如 RNA 测序(RNA-Seq))的高质量总 RNA。目前从关节软骨细胞中提取高质量 RNA 的方法不一致,导致产量不理想,质量受损。这在将 RNA-Seq 应用于研究软骨转录组方面带来了重大困难。目前的方法要么依赖于胶原酶消化来解离软骨细胞外基质,要么在 RNA 提取之前使用各种方法粉碎软骨。然而,根据体内软骨的种类和来源,软骨处理的方案差异很大。有从人或大哺乳动物(如马或牛)软骨样本中分离 RNA 的方案,但鸡软骨的方案却没有,尽管该物种在软骨研究中被广泛使用。在这里,我们提出了两种基于使用低温研磨机粉碎新鲜关节软骨或使用 1.2%(w/v)胶原酶 II 进行酶消化的改进 RNA 分离方案。我们的方案优化了收集和组织处理步骤,以最大限度地减少 RNA 降解并提高 RNA 纯度。我们的结果表明,使用这些方法从鸡关节软骨中纯化的 RNA 适合用于 RNA-Seq 实验。该程序适用于从狗、猫、绵羊和山羊等其他物种的软骨中提取 RNA。这里还描述了 RNA-Seq 分析的工作流程。© 2023 作者。Wiley Periodicals LLC 出版的《当代方案》。基础方案 1:从粉碎的鸡关节软骨中提取总 RNA 备选方案 1:从胶原消化的关节软骨中提取总 RNA 支持方案 1:从膝关节中分离鸡关节软骨 基础方案 2:从鸡关节软骨总 RNA 进行 RNA 测序。