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首页> 外文期刊>Phytotherapy research: PTR >Inhibition of Ulmus davidiana Planch (Ulmaceae) on bone resorption mediated by processing of cathepsin K in cultured mouse Osteoclasts
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Inhibition of Ulmus davidiana Planch (Ulmaceae) on bone resorption mediated by processing of cathepsin K in cultured mouse Osteoclasts

机译:组织培养的破骨细胞对组织蛋白酶K介导的榆叶榆(Ulmaceae)对骨吸收的抑制作用

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摘要

Ulmus davidiana Planch (Ulmaceae) (UD) has long been known to be antiinflammatory in traditional Korean medicine. This experiment investigated the effects of UD on bone resorption using bone cell culture. Different concentrations of crude extract of UD were added to mouse bone cell culture. The mitochondrial activity of the bone cells after exposure of UD was determined by colorimetric 3-(4,5-dimethylthiazolyl-2)2,5-diphenyltetrazolium bromide (MTT). It was demonstrated that UD has potential effects on bone cell culture without cytotoxicity. The most effective concentration of UD in bone cells was 100 mu g/mL. Cathepsin K (Cat K) is the major cysteine protease expressed in osteoclasts and is thought to play a key role in matrix degradation during bone resorption. When mouse long bone cells including osteoclasts and osteoblasts were treated with UD, UD prevented the osteoclast-mediated intracellular processing of Cat K, suggesting that UD may disrupt the intracellular transport of pro Cat K. Since secreted proenzymes have the potential to reenter the cell via the mannose-6-phosphate (M6P) receptor, to prevent this possibility, UD was tested in the absence or presence of M6P. Inhibition of Cat K processing by UD was observed in a dose-dependent manner. Furthermore, the addition of M6P resulted in enhanced potency of UD. UD dose-dependently inhibited in vitro bone resorption with a potency similar to that observed for inhibition of Cat K processing. Copyright (c) 2008 John Wiley & Sons, Ltd.
机译:榆树(Ulmaceae)(UD)在韩国传统医学中具有抗炎作用。该实验研究了UD对使用骨细胞培养的骨吸收的影响。将不同浓度的UD粗提取物添加到小鼠骨细胞培养物中。 UD暴露后骨细胞的线粒体活性通过比色3-(4,5-二甲基噻唑基-2)2,5-二苯基四唑溴化物(MTT)确定。已经证明UD对骨细胞培养具有潜在的影响而没有细胞毒性。骨细胞中UD的最有效浓度为100μg / mL。组织蛋白酶K(Cat K)是破骨细胞中表达的主要半胱氨酸蛋白酶,被认为在骨吸收过程中对基质降解起关键作用。当用UD处理小鼠的长骨细胞(包括破骨细胞和成骨细胞)时,UD阻止了破骨细胞介导的Cat K的细胞内加工,这表明UD可能破坏pro Cat K的细胞内运输。由于分泌的酶有可能通过为了防止这种可能性,使用了6磷酸甘露糖(M6P)受体来检测UD的存在或不存在。 UD对Cat K加工的抑制作用呈剂量依赖性。此外,M6P的添加导致UD的效力增强。 UD剂量依赖性地抑制体外骨吸收,其效力类似于对Cat K加工的抑制作用。版权所有(c)2008 John Wiley&Sons,Ltd.

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