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Current Status and Strategy of microRNA Research for Cartilage Development and Osteoarthritis Pathogenesis

机译:软骨发育和骨关节炎发病机制的microRNA研究现状和策略

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摘要

MicroRNAs (miRNAs), which are small (~21 nucleotides) non-coding RNAs, are important players in endochondral ossification, articular cartilage homeostasis, and arthritis pathogenesis. Comprehensive and genetic analyses of cartilage-specific or cartilage-related miRNAs have provided new information on cartilage development, homeostasis, and related diseases. State-of-the-art combinatorial approaches, including transcription-activator like effector nuclease (TALEN)/clustered regularly interspaced short palindromic repeats (CRISPR) technique for targeting miRNAs and high-throughput sequencing of RNA isolated by cross-linking immunoprecipitation for identifying target messenger RNAs, should be used to determine complex miRNA networks and miRNA-dependent cartilage regulation. Use of advanced drug delivery systems involving cartilage-specific miRNAs will accelerate the application of these new findings in arthritis therapy.
机译:小RNA(miRNA)是小的(〜21个核苷酸)非编码RNA,是软骨内骨化,关节软骨稳态和关节炎发病机制中的重要角色。软骨特异性或与软骨相关的miRNA的全面和遗传分析已提供了有关软骨发育,体内平衡和相关疾病的新信息。最先进的组合方法,包括转录激活物(如效应子核酸酶(TALEN)/聚簇的规则间隔的短回文重复序列(CRISPR)技术)靶向miRNA,以及通过交联免疫沉淀法分离的RNA高通量测序以鉴定靶标信使RNA,应用于确定复杂的miRNA网络和miRNA依赖性软骨调节。使用涉及软骨特异性miRNA的先进药物递送系统将加速这些新发现在关节炎治疗中的应用。

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