Tianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for Cancer, West Huan-Hu Road, Ti Yuan Bei, Hexi District, Tianjin, 30060, PR China.
Tianjin's Clinical Research Center for Cancer, West Huan-Hu Road, Ti Yuan Bei, Hexi District, Tianjin, 30060, PR China.
BMC Oral Health. 2024 Feb 28;24(1):284. doi: 10.1186/s12903-024-03971-x.
Investigating the molecular biology underpinning the early-stage of traumatic temporomandibular joint (TMJ) ankylosis is crucial for discovering new ways to prevent the disease. This study aimed to explore the dynamic changes of transcriptome from the intra-articular hematoma or the newly generated ankylosed callus during the onset and early progression of TMJ ankylosis.
Based on a well-established sheep model of TMJ bony ankylosis, the genome-wide microarray data were obtained from samples at postoperative Days 1, 4, 7, 9, 11, 14 and 28, with intra-articular hematoma at Day 1 serving as controls. Fold changes in gene expression values were measured, and genes were identified via clustering based on time series analysis and further categorised into three major temporal classes: increased, variable and decreased expression groups. The genes in these three temporal groups were further analysed to reveal pathways and establish their biological significance.
Osteoblastic and angiogenetic genes were found to be significantly expressed in the increased expression group. Genes linked to inflammation and osteoclasts were found in the decreased expression group. The various biological processes and pathways related to each temporal expression group were identified, and the increased expression group comprised genes exclusively involved in the following pathways: Hippo signaling pathway, Wnt signaling pathway and Rap 1 signaling pathway. The decreased expression group comprised genes exclusively involved in immune-related pathways and osteoclast differentiation. The variable expression group consisted of genes associated with DNA replication, DNA repair and DNA recombination. Significant biological pathways and transcription factors expressed at each time point postoperatively were also identified.
These data, for the first time, presented the temporal gene expression profiling and reveal the important process of molecular biology in the early-stage of traumatic TMJ bony ankylosis. The findings might contributed to identifying potential targets for the treatment of TMJ ankylosis.
研究创伤性颞下颌关节(TMJ)强直早期的分子生物学基础对于发现预防该疾病的新方法至关重要。本研究旨在探讨 TMJ 强直发病和早期进展过程中关节内血肿或新形成的强直骨痂的转录组的动态变化。
基于建立良好的羊 TMJ 骨性强直模型,从术后第 1、4、7、9、11、14 和 28 天的样本中获得全基因组微阵列数据,第 1 天的关节内血肿作为对照。测量基因表达值的倍数变化,并通过基于时间序列分析的聚类来鉴定基因,并进一步分为三大时间类别:表达增加、表达可变和表达减少组。对这三个时间组中的基因进行进一步分析,以揭示通路并确定其生物学意义。
在表达增加组中发现成骨和成血管基因显著表达。在表达减少组中发现与炎症和破骨细胞相关的基因。确定了与每个时间表达组相关的各种生物学过程和途径,表达增加组仅包含参与以下途径的基因:Hippo 信号通路、Wnt 信号通路和 Rap1 信号通路。表达减少组仅包含与免疫相关途径和破骨细胞分化相关的基因。可变表达组包含与 DNA 复制、DNA 修复和 DNA 重组相关的基因。还确定了术后每个时间点表达的显著生物学途径和转录因子。
这些数据首次提供了 TMJ 骨性强直早期的时间基因表达谱,并揭示了分子生物学的重要过程。研究结果可能有助于确定 TMJ 强直治疗的潜在靶点。