The Affiliated Hospital of Medical College, Qingdao University, Qingdao, Shandong 266001, PR China.
Carbohydr Polym. 2013 Jan 30;92(1):824-9. doi: 10.1016/j.carbpol.2012.09.043. Epub 2012 Sep 29.
The aim of this study was to evaluate the effects of chitosan and quaternized chitosan (HTCC) modulate IL-1β and TNF-α in LPS-stimulated human periodontal ligament cells (HPDLCs). MTT assay revealed that chitosan stimulated the proliferation of HPDLCs. However, HTCC inhibited the proliferation of HPDLCs at concentrations of 1000 and 100 μg/mL more than the control, especially after 5d (P<0.001). ELISA assay exhibited that chitosan inhibited the production of IL-1β and TNF-α at 24, 48 and 72 h. IL-1β and TNF-α secreted by HPDLCs with LPS and treated with 1000 μg/mL of HTCC significantly increased compared to both the control and the chitosan group (P<0.001). The bioactive role for bFGF in modulating the responses of HPDLCs cells to LPS via inhibiting IL-1β and TNF-α production was demonstrated. All results were necessary to enhance our understanding of the biomedical properties of chitosan and HTCC for modulation of pro-inflammatory mediators.
本研究旨在评估壳聚糖和季铵化壳聚糖(HTCC)对脂多糖刺激的人牙周韧带细胞(HPDLCs)中白细胞介素 1β(IL-1β)和肿瘤坏死因子-α(TNF-α)的调节作用。MTT 分析显示壳聚糖能刺激 HPDLCs 的增殖。然而,HTCC 在浓度为 1000 和 100 μg/mL 时,对 HPDLCs 的增殖抑制作用比对照组更强,尤其是在 5 天后(P<0.001)。ELISA 分析表明,壳聚糖能抑制 24、48 和 72 小时时 IL-1β和 TNF-α的产生。与对照组和壳聚糖组相比,用 LPS 处理并用 1000 μg/mL 的 HTCC 处理的 HPDLCs 分泌的 IL-1β 和 TNF-α 明显增加(P<0.001)。bFGF 通过抑制 IL-1β 和 TNF-α 的产生,对 HPDLCs 细胞对 LPS 的反应具有生物活性调节作用。所有结果都有助于我们理解壳聚糖和 HTCC 对促炎介质的调节的生物医学特性。