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转录组分析揭示了与创伤后骨关节炎进展中软骨退化相关的新基因。

Transcriptome Analysis Reveals Novel Genes Associated with Cartilage Degeneration in Posttraumatic Osteoarthritis Progression.

机构信息

Department of Anesthesiology, Taipei Medical University Hospital, Taipei, Taiwan.

Department of Anesthesiology, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.

出版信息

Cartilage. 2021 Dec;13(2_suppl):1249S-1262S. doi: 10.1177/1947603519847744. Epub 2019 May 20.

Abstract

OBJECTIVE

The current therapeutic strategy for posttraumatic osteoarthritis (PTOA) focuses on early intervention to attenuate disease progression, preserve joint function, and defer joint replacement timing. Sequential transcriptomic changes of articular cartilage in a rat model were investigated to explore the molecular mechanism in early PTOA progression.

DESIGN

Anterior cruciate ligament transection and medial meniscectomy (ACLT + MMx)-induced PTOA model was applied on male Wistar rats. Articular cartilages were harvested at time 0 (naïve), 2 week, and 4 weeks after surgery. Affymetrix Rat genome 230 2.0 array was utilized to analyze the gene expression changes of articular cartilages.

RESULTS

We identified 849 differentially expressed genes (DEGs) at 2 weeks and 223 DEGs at 4 weeks post-ACLT + MMx surgery compared with time 0 (naïve group). Gene ontology and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis were performed to gain further insights from these DEGs. 22 novel genes and 1 novel KEGG pathway (axon guidance) in cartilage degeneration of osteoarthritis were identified. Axon guidance molecules-, and commonly dysregulated in PTOA progression. gene showed a concordant change in protein expression by immunohistochemistry staining.

CONCLUSIONS

Our study identified 22 novel dysregulated genes and axon guidance pathway associated with articular cartilage degeneration in PTOA progression. These findings provide the potential candidates of biomarkers and therapeutic targets for further investigation.

摘要

目的

外伤性骨关节炎(PTOA)的当前治疗策略侧重于早期干预以减轻疾病进展、保持关节功能并推迟关节置换时间。本研究通过研究关节软骨在大鼠模型中的连续转录组变化,探讨早期 PTOA 进展中的分子机制。

设计

应用前交叉韧带切断和内侧半月板切除术(ACLT + MMx)诱导的 PTOA 模型对雄性 Wistar 大鼠进行处理。在手术后 0(天真)、2 周和 4 周时采集关节软骨。利用 Affymetrix Rat genome 230 2.0 芯片分析关节软骨的基因表达变化。

结果

与 0 时间(天真组)相比,ACLT + MMx 手术后 2 周和 4 周分别有 849 个差异表达基因(DEGs)和 223 个 DEGs。对这些 DEGs 进行基因本体论和京都基因与基因组百科全书(KEGG)通路分析,以获得更深入的见解。在软骨退变的骨关节炎中鉴定出 22 个新的基因和 1 个新的 KEGG 通路(轴突导向)。在 PTOA 进展中,轴突导向分子和通常失调。免疫组织化学染色显示基因的蛋白表达也呈一致变化。

结论

本研究确定了 22 个新的失调基因和与 PTOA 进展中关节软骨退化相关的轴突导向通路。这些发现为进一步研究提供了潜在的生物标志物和治疗靶点候选物。

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