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EFFECT OF INFLAMMATION ON THE OSMOTIC RESPONSE OF NUCLEUS PULPOSUS CELLS

机译:发炎对髓核细胞渗透反应的影响

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Intervertebral disc (IVD) degeneration is accompanied by elevated levels of pro-inflammatory cytokines, particularly IL-1β and TNF-α [1]. Disc cells from the nucleus pulposus (NPs) respond to cytokine stimulation with increased catabolic breakdown of the tissue, resulting in a positive feedback of disc integrity loss and further inflammation [2]. Previous studies by our group have examined the response of NP cells to Toll-Like Receptor-4 (TLR-4) activation through stimulation with lipopolysaccharide (LPS). TLR-4 is a pattern recognition receptor that is activated in innate immunity and by polysaccharide fragments from degenerated proteoglycans. TLR-4 activation by LPS results in stimulation of multiple cytokines by NP cells [3]. Moreover, we have shown that in vivo LPS injection results in catabolic changes in the IVD, including matrix breakdown, decrease in biomechanical properties and loss of disc height [4]. However, the specific cellular mechanisms for these catabolic changes remain to be elucidated.
机译:椎间盘退变(IVD)伴随着促炎性细胞因子,特别是IL-1β和TNF-α的升高[1]。髓核(NPs)的椎间盘细胞对细胞因子的刺激作出反应,组织分解代谢增加,导致椎间盘完整性丧失和进一步炎症的积极反馈[2]。我们小组先前的研究已经检查了NP细胞通过脂多糖(LPS)刺激对Toll样受体4(TLR-4)活化的反应。 TLR-4是一种模式识别受体,在先天免疫中被变性蛋白聚糖的多糖片段激活。 LPS激活TLR-4会导致NP细胞刺激多种细胞因子[3]。此外,我们已经表明,体内LPS注射会导致IVD分解代谢变化,包括基质分解,生物力学性能下降和椎间盘高度降低[4]。然而,这些分解代谢变化的具体细胞机制仍有待阐明。

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