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壳聚糖和季铵化壳聚糖对脂多糖刺激的人牙周韧带细胞促炎介质的调节作用。

Modulation of pro-inflammatory mediators in LPS-stimulated human periodontal ligament cells by chitosan and quaternized chitosan.

机构信息

The Affiliated Hospital of Medical College, Qingdao University, Qingdao, Shandong 266001, PR China.

出版信息

Carbohydr Polym. 2013 Jan 30;92(1):824-9. doi: 10.1016/j.carbpol.2012.09.043. Epub 2012 Sep 29.

Abstract

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.

摘要

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。

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