木瓜乙醇提取物对核因子κ B配体介导的破骨细胞发生受体激活物的抑制作用

G. Park, D. Gu, Seoung‐Hoon Lee
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引用次数: 0

摘要

在韩国被称为“毛瓜”的木瓜果实在传统医学中被广泛用于治疗喉咙痛等炎症性疾病。然而,其对骨代谢的影响尚不清楚。本实验研究了木瓜果乙醇提取物(CFE)对核因子-κB受体激活剂(RANKL)介导的破骨细胞分化和形成的影响。CF-E以剂量依赖的方式显著抑制骨髓源性巨噬细胞和破骨细胞前体细胞的破骨细胞分化和抗酒石酸酸性磷酸酶阳性多核细胞形成。此外,与未处理的对照细胞相比,cf - e处理的破骨细胞中肌动蛋白环和吸收坑的形成明显受到抑制。与这些表型抑制结果一致,CF-E处理显著降低了破骨细胞分化标志基因(Acp5、Atp6v0d2、Oscar、CtsK和Tm7sf4)和破骨细胞生成关键转录因子Nfatc1的表达。CF-E对rankl诱导的破骨细胞形成的抑制作用与抑制NFATc1表达有关,而不是通过调节丝裂原活化蛋白激酶和NF-κB活化,而是通过磷脂酶C γ 1和2的失活。这些结果表明,CF-E对破骨细胞的分化和形成具有抑制作用,并提示CF-E可能作为骨吸收性疾病(如骨质疏松症、类风湿关节炎和牙周炎)的传统治疗剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibitory effect of Chaenomelis Fructus ethanol extract on receptor activator of nuclear factor-kappa B ligand-mediated osteoclastogenesis
The fruit of Chaenomeles sinensis (Thouin) Koehne (Chaenomelis Fructus) known as “Mo-Gua” in Korea has been commonly used in traditional medicine to treat inflammatory diseases, such as sore throat. However, its effect on bone metabolism has not been elucidated yet. Here, we examined the effect of Chaenomelis Fructus ethanol extract (CFE) on receptor activator of nuclear factor (NF)-κB ligand (RANKL)-mediated osteoclast differentiation and formation. CF-E considerably inhibited osteoclast differentiation and tartrate-resistant acid phosphatase-positive multinuclear cell formation from bone marrow-derived macrophages and osteoclast precursor cells in a dose-dependent manner. In addition, the formation of actin rings and resorption pits were significantly suppressed in CF-E-treated osteoclasts as compared with the findings in non-treated control cells. Consistent with these phenotypic inhibitory results, the expressions of osteoclast differentiation marker genes (Acp5, Atp6v0d2 , Oscar, CtsK, and Tm7sf4) and Nfatc1 , a pivotal transcription factor for osteoclastogenesis, were markedly decreased by CF-E treatment. The inhibitory effect of CF-E on RANKL-induced osteoclastogenesis was associated with the suppression of NFATc1 expression, not by regulation of mitogen-activated protein kinases and NF-κB activation but by the inactivation of phospholipase C gamma 1 and 2. These results indicate that CF-E has an inhibitory effect on osteoclast differentiation and formation, and they suggest the possibility of CF-E as a traditional therapeutic agent against bone-resorptive diseases, such as osteoporosis, rheumatoid arthritis, and periodontitis.
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