Qiao Linghui, Gu Jun, Ni Yingjie, Wu Jianyue, Zhang Dong, Gu Yanglin
Wuxi Xishan People's Hospital (Wuxi Branch of Zhongda Hospital Affiliated to Southeast University), Wuxi 214000, China.
Department of Orthopedics, Jiangnan University Medical Center, Wuxi 214000, China.
J Clin Med. 2023 Feb 11;12(4):1449. doi: 10.3390/jcm12041449.
Osteoarthritis (OA) is a chronic disease common in the elderly population and imposes significant health and economic burden. Total joint replacement is the only currently available treatment but does not prevent cartilage degeneration. The molecular mechanism of OA, especially the role of inflammation in disease progression, is incompletely understood. We collected knee joint synovial tissue samples of eight OA patients and two patients with popliteal cysts (controls), measured the expression levels of lncRNAs, miRNAs, and mRNAs in these tissues by RNA-seq, and identified differentially expressed genes (DEGs) and key pathways. In the OA group, 343 mRNAs, 270 lncRNAs, and 247 miRNAs were significantly upregulated, and 232 mRNAs, 109 lncRNAs, and 157 miRNAs were significantly downregulated. mRNAs potentially targeted by lncRNAs were predicted. Nineteen overlapped miRNAs were screened based on our sample data and GSE 143514 data. Pathway enrichment and functional annotation analyses showed that the inflammation-related transcripts , miR-146a-5p, miR-335-5p, lncRNA GAS5, LINC02288, and LOC101928134 were differentially expressed. In this study, inflammation-related DEGs and non-coding RNAs were identified in synovial samples, suggesting that competing endogenous RNAs have a role in OA. TREM1, LIF, miR146-5a, and GAS5 were identified to be OA-related genes and potential regulatory pathways. This research helps elucidate the pathogenesis of OA and identify novel therapeutic targets for this disorder.
骨关节炎(OA)是一种在老年人群中常见的慢性疾病,会带来重大的健康和经济负担。全关节置换是目前唯一可用的治疗方法,但无法预防软骨退变。OA的分子机制,尤其是炎症在疾病进展中的作用,尚未完全明确。我们收集了8例OA患者和2例腘窝囊肿患者(对照组)的膝关节滑膜组织样本,通过RNA测序测量了这些组织中lncRNA、miRNA和mRNA的表达水平,并鉴定了差异表达基因(DEG)和关键通路。在OA组中,343个mRNA、270个lncRNA和247个miRNA显著上调,232个mRNA、109个lncRNA和157个miRNA显著下调。预测了可能被lncRNA靶向的mRNA。基于我们的样本数据和GSE 143514数据筛选出19个重叠的miRNA。通路富集和功能注释分析表明,炎症相关转录本、miR-146a-5p、miR-335-5p、lncRNA GAS5、LINC02288和LOC101928134存在差异表达。在本研究中,在滑膜样本中鉴定出炎症相关的DEG和非编码RNA,提示竞争性内源RNA在OA中发挥作用。TREM1、LIF、miR146-5a和GAS5被鉴定为与OA相关的基因和潜在调控通路。本研究有助于阐明OA的发病机制,并确定该疾病的新治疗靶点。