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动态机械压缩影响接种于琼脂糖中的关节软骨细胞产生一氧化氮。

Dynamic mechanical compression influences nitric oxide production by articular chondrocytes seeded in agarose.

作者信息

Lee D A, Frean S P, Lees P, Bader D L

机构信息

IRC in Biomedical Materials, Institute of Orthopaedics, University College London Medical School, Brockley Hill, Stanmore, Middlesex, HA7 4LP, United Kingdom.

出版信息

Biochem Biophys Res Commun. 1998 Oct 20;251(2):580-5. doi: 10.1006/bbrc.1998.9520.

Abstract

Nitric oxide (NO) has been implicated in the inhibition of cell proliferation in cytokine and lipopolysaccharide (LPS)-stimulated chondrocytes and is known to be influenced by physical forces in several tissues. In this study, a well-characterized model system utilizing bovine chondrocytes embedded in 3% agarose constructs has been used to investigate the effect of dynamic strain at 0.3, 1, or 3 Hz on NO production. LPS induced a significant increase in nitrite levels, which was reversed by both L-NAME and dexamethasone. Dynamic compressive strain produced a significant reduction in nitrite production. The effect was partially blocked by L-NAME but unaffected by dexamethasone. L-NAME also reversed dynamic compression-induced stimulation of [3H]-thymidine incorporation. NO appears to be a constituent of mechanotransduction pathways which influence proliferation of bovine chondrocytes seeded within agarose constructs. The inhibitor experiments also infer that alterations in cNOS activity primarily determine the response.

摘要

一氧化氮(NO)与细胞因子和脂多糖(LPS)刺激的软骨细胞的细胞增殖抑制有关,并且已知在几种组织中受物理力影响。在本研究中,利用嵌入3%琼脂糖构建体中的牛软骨细胞的特征明确的模型系统,来研究0.3、1或3Hz的动态应变对NO产生的影响。LPS诱导亚硝酸盐水平显著升高,L-NAME和地塞米松均可使其逆转。动态压缩应变使亚硝酸盐产生显著降低。该效应部分被L-NAME阻断,但不受地塞米松影响。L-NAME还逆转了动态压缩诱导的[3H]-胸苷掺入刺激。NO似乎是影响琼脂糖构建体中接种的牛软骨细胞增殖的机械转导途径的一个组成部分。抑制剂实验还推断,cNOS活性的改变主要决定了这种反应。

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