Institute of Anatomy and Cell Biology, Paracelsus Medical University, Nuremberg and Salzburg, General Hospital Nuremberg, Prof. Ernst Nathan Str. 1, 90419 Nuremberg, Germany.
Department of Traumatology and Reconstructive Surgery, Campus Benjamin Franklin, Charité-Universitätsmedizin Berlin, Corporate Member of Berlin Institute of Health, Freie Universität Berlin and Humboldt-Universität zu Berlin, Hindenburgdamm 30, 12203 Berlin, Germany.
Int J Mol Sci. 2021 Mar 18;22(6):3105. doi: 10.3390/ijms22063105.
A central part of the complement system, the anaphylatoxin C5a was investigated in this study to learn its effects on tenocytes in respect to understanding the potential expression of other crucial complement factors and pro-inflammatory mediators involved in tendinopathy. Human hamstring tendon-derived tenocytes were treated with recombinant C5a protein in concentrations of 25 ng/mL and 100 ng/mL for 0.5 h (early phase), 4 h (intermediate phase), and 24 h (late phase). Tenocytes survival was assessed after 24 h stimulation by live-dead assay. The gene expression of complement-related factors C5aR, the complement regulatory proteins (CRPs) CD46, CD55, CD59, and of the pro-inflammatory cytokines tumor necrosis factor (TNF)-α and interleukin (IL)-6 was monitored using qPCR. Tenocytes were immunolabeled for C5aR and CD55 proteins. TNFα production was monitored by ELISA. Tenocyte survival was not impaired through C5a stimulation. Interestingly, the gene expression of C5aR and that of the CRPs CD46 and CD59 was significantly reduced in the intermediate and late phase, and that of TNFα only in an early phase, compared to the control group. ELISA analysis indicated a concomitant not significant trend of impaired TNFα protein synthesis at 4 h. However, there was also an early significant induction of CD55 and CD59 mediated by 25 ng/mL anaphylatoxin C5a. Hence, exposure of tenocytes to C5a obviously evokes a time and concentration-dependent response in their expression of complement and pro-inflammatory factors. C5a, released in damaged tendons, might directly contribute to tenocyte activation and thereby be involved in tendon healing and tendinopathy.
补体系统的核心部分,过敏毒素 C5a 在这项研究中进行了研究,以了解其对腱细胞的影响,从而了解参与腱病的其他关键补体因子和促炎介质的潜在表达。用人的腘绳肌腱衍生的腱细胞用浓度为 25ng/ml 和 100ng/ml 的重组 C5a 蛋白处理 0.5 小时(早期阶段)、4 小时(中期阶段)和 24 小时(晚期阶段)。用活/死测定法在 24 小时刺激后评估腱细胞的存活率。使用 qPCR 监测补体相关因子 C5aR、补体调节蛋白(CRPs)CD46、CD55、CD59 和促炎细胞因子肿瘤坏死因子(TNF)-α和白细胞介素(IL)-6 的基因表达。用免疫细胞化学法标记 C5aR 和 CD55 蛋白。通过 ELISA 监测 TNFα 的产生。C5a 刺激不会损害腱细胞的存活率。有趣的是,与对照组相比,C5aR 和 CRPs CD46 和 CD59 的基因表达在中期和晚期显著降低,而 TNFα 的基因表达仅在早期阶段降低。ELISA 分析表明,在 4 小时时 TNFα 蛋白合成受损的趋势不显著。然而,在 25ng/ml 过敏毒素 C5a 的作用下,也会早期显著诱导 CD55 和 CD59。因此,C5a 暴露于腱细胞明显会引起补体和促炎因子表达的时间和浓度依赖性反应。在受损的肌腱中释放的 C5a 可能直接促进腱细胞的激活,从而参与肌腱愈合和腱病。