Department of Orthopaedic Surgery, Washington University, St Louis, United States.
Shriners Hospitals for Children, St. Louis, United States.
Elife. 2020 Mar 23;9:e49558. doi: 10.7554/eLife.49558.
The roles of long noncoding RNAs (lncRNAs) in musculoskeletal development, disease, and regeneration remain poorly understood. Here, we identified the novel lncRNA (originally named ) as a regulator of mesenchymal stem cell (MSC) chondrogenesis. , a primate-specific lncRNA, is upregulated during MSC chondrogenesis and appears to act directly downstream of SOX9, but not TGF-β3. We showed that the silencing of resulted in lower accumulation of cartilage-like extracellular matrix in a pellet assay, while overexpression - either via transgene ectopic expression or by endogenous activation via CRISPR-dCas9-VP64 - significantly enhanced cartilage matrix production. acts to inhibit IFN-γ by binding to EIF2AK2, and we further demonstrated that exhibits a protective effect in engineered cartilage against interferon type II. Our results indicate an important role of in regulating stem cell chondrogenesis, as well as its therapeutic potential in the treatment of cartilage-related diseases, such as osteoarthritis.
长链非编码 RNA(lncRNAs)在肌肉骨骼发育、疾病和再生中的作用仍知之甚少。在这里,我们鉴定了一个新的 lncRNA(最初命名为 )作为间充质干细胞(MSC)成软骨分化的调节剂。是一种灵长类特异性 lncRNA,在 MSC 成软骨分化过程中上调,似乎直接作用于 SOX9 下游,但不作用于 TGF-β3。我们表明,沉默 导致微球体培养中软骨样细胞外基质的积累减少,而 过表达——无论是通过转基因异位表达还是通过 CRISPR-dCas9-VP64 内源性激活——显著增强软骨基质的产生。通过与 EIF2AK2 结合来抑制 IFN-γ,我们进一步证明 在针对 II 型干扰素的工程软骨中表现出保护作用。我们的结果表明 在调节干细胞成软骨分化中具有重要作用,并且在治疗与软骨相关的疾病(如骨关节炎)方面具有治疗潜力。