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锌和铜掺杂的生物活性溶胶-凝胶玻璃对脂多糖刺激的RAW 264.7小鼠巨噬细胞炎症反应的抑制作用

Abrogation of the inflammatory response in LPS-stimulated RAW 264.7 murine macrophages by Zn- and Cu-doped bioactive sol-gel glasses.

作者信息

Varmette Elizabeth A, Nowalk Jessica R, Flick Lisa M, Hall Matthew M

机构信息

SCHOTT North America, Inc., 400 York Avenue, Duryea, Pennsylvania 18642, USA.

出版信息

J Biomed Mater Res A. 2009 Aug;90(2):317-25. doi: 10.1002/jbm.a.32098.

Abstract

The attenuation of an in vitro inflammatory response in RAW 264.7 murine macrophages stimulated with lipopolysaccharide (LPS) endotoxin was tested using sol-gel-derived bioactive glasses. Three general types of sol-gel-derived samples were evaluated: 58S, zinc-containing glasses, and copper-containing glasses. Distinct experimental procedures were used to test the potential of bioactive glasses to attenuate the inflammatory response in three situations: (1) therapeutically following LPS stimulation, (2) prophylactically before LPS stimulation of macrophages, and (3) indirectly via the glass dissolution products after stimulation with LPS. A sandwich enzyme-linked immunosorbent assay (ELISA) was used to monitor the concentration of tumor necrosis factor-alpha (TNF-alpha) secreted by macrophage cells. The strongest reduction in TNF-alpha concentration was observed when macrophage cells were first incubated with bioactive glass powder and then stimulated with LPS. This suggests a possible prophylactic application of these bioactive glasses for the prevention of inflammation. The 58S glass was capable of reducing the expression of TNF-alpha by macrophages, although the zinc- and copper-containing were more effective at suppressing the inflammatory response. The additional benefit of using zinc- and copper-doped bioactive glasses may be explained by the direct interactions of zinc and copper ions in key regulatory pathways for the inflammation response.

摘要

使用溶胶 - 凝胶法制备的生物活性玻璃测试了脂多糖(LPS)内毒素刺激的RAW 264.7小鼠巨噬细胞体外炎症反应的减弱情况。评估了三种一般类型的溶胶 - 凝胶法制备的样品:58S、含锌玻璃和含铜玻璃。采用不同的实验程序来测试生物活性玻璃在三种情况下减弱炎症反应的潜力:(1)在LPS刺激后进行治疗,(2)在巨噬细胞受到LPS刺激之前进行预防,以及(3)在LPS刺激后通过玻璃溶解产物间接发挥作用。采用夹心酶联免疫吸附测定法(ELISA)监测巨噬细胞分泌的肿瘤坏死因子 - α(TNF - α)的浓度。当巨噬细胞先与生物活性玻璃粉末孵育然后再用LPS刺激时,观察到TNF - α浓度的最大降低。这表明这些生物活性玻璃在预防炎症方面可能有预防性应用。58S玻璃能够降低巨噬细胞TNF - α的表达,尽管含锌和含铜玻璃在抑制炎症反应方面更有效。使用掺杂锌和铜的生物活性玻璃的额外益处可能是由锌和铜离子在炎症反应关键调节途径中的直接相互作用来解释的。

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