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首页> 外文期刊>BMC Musculoskeletal Disorders >Temporal gene expression profiling of the rat knee joint capsule during immobilization-induced joint contractures
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Temporal gene expression profiling of the rat knee joint capsule during immobilization-induced joint contractures

机译:大鼠膝关节胶囊在固定诱导的关节挛缩期间的颞基因表达谱

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Background Contractures of the knee joint cause disability and handicap. Recovering range of motion is recognized by arthritic patients as their preference for improved health outcome secondary only to pain management. Clinical and experimental studies provide evidence that the posterior knee capsule prevents the knee from achieving full extension. This study was undertaken to investigate the dynamic changes of the joint capsule transcriptome during the progression of knee joint contractures induced by immobilization. We performed a microarray analysis of genes expressed in the posterior knee joint capsule following induction of a flexion contracture by rigidly immobilizing the rat knee joint over a time-course of 16?weeks. Fold changes of expression values were measured and co-expressed genes were identified by clustering based on time-series analysis. Genes associated with immobilization were further analyzed to reveal pathways and biological significance and validated by immunohistochemistry on sagittal sections of knee joints. Results Changes in expression with a minimum of 1.5 fold changes were dominated by a decrease in expression for 7732 probe sets occurring at week 8 while the expression of 2251 probe sets increased. Clusters of genes with similar profiles of expression included a total of 162 genes displaying at least a 2 fold change compared to week 1. Functional analysis revealed ontology categories corresponding to triglyceride metabolism, extracellular matrix and muscle contraction. The altered expression of selected genes involved in the triglyceride biosynthesis pathway; AGPAT-9, and of the genes P4HB and HSP47, both involved in collagen synthesis, was confirmed by immunohistochemistry. Conclusions Gene expression in the knee joint capsule was sensitive to joint immobility and provided insights into molecular mechanisms relevant to the pathophysiology of knee flexion contractures. Capsule responses to immobilization was dynamic and characterized by modulation of at least three reaction pathways; down regulation of triglyceride biosynthesis, alteration of extracellular matrix degradation and muscle contraction gene expression. The posterior knee capsule may deploy tissue-specific patterns of mRNA regulatory responses to immobilization. The identification of altered expression of genes and biochemical pathways in the joint capsule provides potential targets for the therapy of knee flexion contractures.
机译:膝关节的背景挛缩导致残疾和障碍。恢复动作范围被关节炎患者认可为其偏好仅对疼痛管理改善的健康结果。临床和实验研究提供了证据表明后膝盖胶囊可防止膝盖实现全延伸。本研究进行了探讨了在固定化诱导的膝关节挛缩进展过程中的关节胶囊转录组的动态变化。通过在16℃的时间过程中刚性地固定大鼠膝关节诱导屈曲挛缩后,在屈曲挛缩后,进行了在后膝关节胶囊中表达的基因的微阵列分析。测量表达值的折叠变化,基于时间序列分析通过聚类鉴定了共表达基因。进一步分析与固定化相关的基因,揭示途径和生物学意义,并通过免疫组织化学在膝关节的矢状部分验证。结果在第8周发生的7732探针组的表达减少时,表达最小的表达变化的变化主要在2251探针组的表达增加。与表达相似的表达曲线的基因簇包括,总共162个基因显示至少2倍的变化,相比是第1周的1.功能分析显示了对应于甘油三酯代谢,细胞外基质和肌肉收缩的本体论类别。参与甘油三酯生物合成途径中所选择的所选基因的改变表达;通过免疫组织化学证实了AGPAT-9,以及涉及胶原合成的基因P4HB和HSP47的基因。结论膝关节胶囊中的基因表达对关节不动敏感,并为膝关节屈曲挛缩病理学的分子机制提供了洞察。胶囊反应的固定性是动态的,并通过调节至少三种反应途径的特征;甘油三酯生物合成的调节,细胞外基质降解的改变和肌肉收缩基因表达。后膝式胶囊可以部署mRNA调节反应的组织特异性模式以固定化。鉴定联合胶囊中基因和生化途径的改变表达提供了膝关节屈曲挛缩治疗的潜在靶标。

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