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Evidence of the TNF-α system in the human achilles tendon: Expression of TNF-α and TNF receptor at both protein and mRNA levels in the tenocytes

机译:人跟腱中TNF-α系统的证据:肌腱细胞中蛋白质和mRNA水平的TNF-α和TNF受体表达

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摘要

Understanding adaption to load is essential for prevention and treatment of tendinopathy/tendinosis. Cytokine release in response to load is one mechanism involved in mechanotransduction. The cytokine tumor necrosis factor alpha (TNF-α) is implicated in tendinosis and can induce apoptotic effects via tumor necrosis factor receptor 1 (TNFR1). The complete absence of information concerning the TNF-α system in Achilles tendon is a limitation as mid-portion Achilles tendinosis is very frequent. Purpose: To examine expression patterns of TNF-α and its two receptors (TNFR1 and TNFR2) in human Achilles tendinosis and control tissue and to biochemically confirm the presence of TNF-α in tendinosis tissue. Methods: TNF-α and TNFR1 mRNA were detected via in situ hybridization. TNF-α, TNFR1, and TNFR2 were demonstrated immunohistochemically. Apoptosis markers were utilized. ELISA was used to detect TNF-α. Results: TNF-α and TNFR1 mRNA was detected in tenocytes of both tendinosis and control tendons. Tenocytes from both groups displayed specific immunoreactions for TNF-α, TNFR1, and TNFR2. The widened/rounded tenocytes of tendinosis samples exhibited the most intense immunoreactions. Apoptosis was detected in only a subpopulation of the tenocytes in tendinosis tissue. TNF-α was measurable in tendinosis tissue. Inflammatory cells were not seen. Conclusion: This is the first evidence of the existence of the TNF-α system in the human Achilles tendon. Findings are confirmed at mRNA and protein levels as well as biochemically. The TNF-α system was in principle confined to the tenocytes. The connection between tenocyte morphology and the expression pattern of TNF-α, TNFR1, and TNFR2 suggests that the TNF-α system may be involved in tenocyte activation in Achilles tendinosis.
机译:了解对负荷的适应性对于预防和治疗肌腱病/肌腱病至关重要。响应负荷而释放细胞因子是机械转导的一种机制。细胞因子肿瘤坏死因子α(TNF-α)与肌腱炎有关,并可通过肿瘤坏死因子受体1(TNFR1)诱导凋亡作用。由于跟腱中部非常常见,因此完全没有关于跟腱中TNF-α系统信息的局限性。目的:研究人跟腱和对照组织中TNF-α及其两个受体(TNFR1和TNFR2)的表达模式,并通过生物化学方法确定肌腱组织中TNF-α的存在。方法:通过原位杂交检测TNF-α和TNFR1 mRNA。免疫组化证实了TNF-α,TNFR1和TNFR2。使用了凋亡标记物。 ELISA用于检测TNF-α。结果:在肌腱和对照肌腱的肌腱细胞中均检测到TNF-α和TNFR1 mRNA。两组的肌腱细胞均表现出针对TNF-α,TNFR1和TNFR2的特异性免疫反应。肌腱病样品的增宽/圆形肌腱细胞表现出最强的免疫反应。仅在肌腱变性组织中的肌腱细胞亚群中检测到凋亡。在肌腱病组织中可测量TNF-α。未见炎性细胞。结论:这是人类跟腱中存在TNF-α系统的第一个证据。在mRNA和蛋白质水平以及生化方面都证实了发现。 TNF-α系统原则上局限于肌腱细胞。肌腱细胞形态与TNF-α,TNFR1和TNFR2表达模式之间的联系表明,TNF-α系统可能参与了跟腱炎的肌腱细胞活化。

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