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首页> 外文期刊>Journal of Endocrinological Investigation: Official Journal of the Italian Society of Endocrinology >Ascorbic acid inhibits osteoclastogenesis of RAW264.7 cells induced by receptor activated nuclear factor kappaB ligand (RANKL) in vitro.
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Ascorbic acid inhibits osteoclastogenesis of RAW264.7 cells induced by receptor activated nuclear factor kappaB ligand (RANKL) in vitro.

机译:抗坏血酸在体外抑制受体激活的核因子κB配体(RANKL)诱导的RAW264.7细胞的破骨细胞生成。

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摘要

Ascorbic acid (AA) plays a key role in the regulation of differentiation and activation of osteoclast (OCL). It was reported that AA might induce the formation of OCL in cocultures of mouse bone marrow cells and ST2 cells, but it is not clear whether AA has a direct impact on the OCL precursors. The purpose of this study was to examine the effect of AA on the differentiation of OCL precursor RAW264.7 cells, cultured with receptor-activated nuclear factor kappaB ligand (RANKL). The results showed that AA remarkably inhibited the cell proliferation at a higher concentration and RANKL alone is sufficient for osteoclastogenesis. The expression of carbonic anhydrase (CAII) mRNA and protein, the number of tartrate-resistant acid phosphatase (TRAP)-positive multinucleated cells (MNCs), and the percentage area of resorption lacunae induced by RANKL were decreased when AA was added to the cultures. The results demonstrate that AA inhibits RANKL-induced differentiation of OCL precursor cells into mature OCL and reduces the formation of bone resorption pits in vitro.
机译:抗坏血酸(AA)在破骨细胞(OCL)分化和激活的调节中起关键作用。据报道,AA可能在小鼠骨髓细胞和ST2细胞的共培养物中诱导OCL的形成,但尚不清楚AA是否对OCL前体有直接影响。这项研究的目的是检验AA对受体激活核因子kappaB配体(RANKL)培养的OCL前体RAW264.7细胞分化的影响。结果显示,AA在较高浓度下能显着抑制细胞增殖,而RANKL单独足以用于破骨细胞生成。加入AA后,碳酸酐酶(CAII)mRNA和蛋白的表达,抗酒石酸酸性磷酸酶(TRAP)阳性的多核细胞(MNC)的数量以及RANKL诱导的再吸收腔的面积减少。 。结果表明,AA可以抑制RANKL诱导的OCL前体细胞分化为成熟的OCL,并在体外减少骨吸收坑的形成。

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