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Dysregulated MiR-3150a-3p Promotes Lumbar Intervertebral Disc Degeneration by Targeting Aggrecan

机译:MiR-3150a-3p失调通过靶向Aggrecan促进腰椎间盘退变

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Background/Aims Low back pain has become one of the most common musculoskeletal diseases in the world. Studies have shown that intervertebral disc degeneration (IDD) is an important factor leading to low back pain, but the mechanisms underlying IDD remain largely unknown. Research over the past decade has suggested critical roles for microRNAs (miRNAs) in natural growth and disease progression. However, it remains poorly understood whether circular RNAs participate in IDD. Methods Clinical IDD samples were collected from 20 patients who underwent discectomy. Weighted gene co-expression network analysis was used to identify the co-expression miRNA network modules (highly co-expressed clusters of miRNAs) that were associated with IDD grade. Results miR-3150a-3p was the most significantly up-regulated miRNA in module “Blue.” Notably, aggrecan (ACAN) was identified as a direct target gene of miR-3150a-3p and ACAN expression was regulated by miR-3150a-3p. Overexpression of miR-3150a-3p decreased ACAN expression in nucleus pulposus cells, whereas inhibition of miR-3150a-3p increased ACAN expression. In addition, ACAN expression was negatively correlated with IDD grade. Conclusion Our study suggests that the reduction of ACAN expression induced by the upregulation of miR-3150a-3p might participate in the development of IDD.
机译:背景/目的腰背痛已成为世界上最常见的肌肉骨骼疾病之一。研究表明,椎间盘退变(IDD)是导致下腰痛的重要因素,但IDD的潜在机制仍不清楚。过去十年的研究表明,microRNA(miRNA)在自然生长和疾病进展中起着至关重要的作用。然而,仍然不清楚环状RNA是否参与IDD。方法收集20例行椎间盘切除术的患者的临床IDD样本。加权基因共表达网络分析用于鉴定与IDD等级相关的共表达miRNA网络模块(miRNA的高度共表达簇)。结果miR-3150a-3p是模块“ Blue”中最显着上调的miRNA。值得注意的是,聚集蛋白聚糖(ACAN)被确定为miR-3150a-3p的直接靶基因,而ACAN表达受miR-3150a-3p调控。 miR-3150a-3p的过表达降低髓核细胞中ACAN的表达,而抑制miR-3150a-3p则增加ACAN的表达。另外,ACAN表达与IDD等级呈负相关。结论我们的研究表明,miR-3150a-3p上调引起的ACAN表达降低可能参与了IDD的发展。

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