Department for Trauma and Reconstructive Surgery, Charité-Universitätsmedizin, Campus Benjamin Franklin, FEM, Krahmerstr. 6-10, 12207 Berlin, Germany.
J Orthop Res. 2010 Aug;28(8):1071-7. doi: 10.1002/jor.21079.
Tendon injury induces a local inflammatory response, characterized by the induction of pro-inflammatory cytokines. The aim of the present study was to analyze the effects of TNFalpha, IL-6 and IL-10 on key parameters of tendon homeostasis. Cultured primary human tenocytes were treated with the recombinant cytokines IL-6, IL-10, TNFalpha, or combinations of TNFalpha with IL-6 and IL-10 (10 ng/mL, 6, 24 h). Expression of type I collagen, elastin, MMP-1, TNFalpha, IL-1beta, IL-6, IL-10, and suppressors of cytokine signaling (SOCS1, 3) was analyzed with the use of RTD-PCR, immunocytochemistry, and Western blot analysis. In response to TNFalpha, tenocytes reduced their type I collagen deposition but increased their elastin gene expression and highly upregulated their expression for MMP-1, pro-inflammatory (TNFalpha, IL-1beta) and immunoregulatory (IL-6, IL-10) cytokines. TNFalpha stimulation augmented SOCS1, whereas SOCS3 expression in tenocytes was also induced by IL-6. The treatment of tenocytes with IL-6 and IL-10 had no effect on cytokine expression. Neither IL-6 nor IL-10 modulated the observed effects of TNFalpha significantly. These results indicate that TNFalpha strongly activates the tenocytes to amplify their own TNFalpha expression and, subsequently, that of other regulatory cytokines and matrix degrading enzymes. However, the impact of IL-6 and IL-10 on tenocytes remains unclear.
肌腱损伤会引起局部炎症反应,其特征是促炎细胞因子的诱导。本研究旨在分析 TNFalpha、IL-6 和 IL-10 对肌腱稳态关键参数的影响。培养的原代人肌腱细胞用重组细胞因子 IL-6、IL-10、TNFalpha 或 TNFalpha 与 IL-6 和 IL-10 的组合(10ng/ml,6、24 小时)处理。使用 RT-PCR、免疫细胞化学和 Western blot 分析分析了 I 型胶原、弹性蛋白、MMP-1、TNFalpha、IL-1beta、IL-6、IL-10 和细胞因子信号转导抑制剂(SOCS1、3)的表达。对 TNFalpha 的反应,肌腱细胞减少其 I 型胶原沉积,但增加其弹性蛋白基因表达,并高度上调其 MMP-1、促炎(TNFalpha、IL-1beta)和免疫调节(IL-6、IL-10)细胞因子的表达。TNFalpha 刺激增强了 SOCS1,而 SOCS3 的表达也被 IL-6 诱导。IL-6 和 IL-10 处理肌腱细胞对细胞因子表达没有影响。IL-6 和 IL-10 均未显著调节 TNFalpha 观察到的作用。这些结果表明,TNFalpha 强烈激活肌腱细胞,放大其自身 TNFalpha 表达,随后放大其他调节细胞因子和基质降解酶的表达。然而,IL-6 和 IL-10 对肌腱细胞的影响仍不清楚。