Yang Xiaobin, Gao Wenjie, Wang Biao, Wang Xiaodong, Guo Hua, Xiao Yuan, Kong Lingbo, Hao Dingjun
Hong-Hui Hospital, Xi'an Jiaotong University College of Medicine, Xi'an, 710054, China.
J Cell Biochem. 2017 Dec;118(12):4479-4486. doi: 10.1002/jcb.26105. Epub 2017 Jun 1.
Picroside II, one of the major components isolated from the seed of natural plant picrorhiza, is widely used in traditional Chinese medicine. The present study was performed to define effects of picroside II on nuclear factor-kappaB ligand (RANKL)-stimulated osteoclast differentiation in vitro and on lipopolysaccharide (LPS)-induced bone loss in vivo. The bone marrow cells (BMMs) were harvested and induced with RANKL followed by treatment with picroside II at several doses, and the differentiation of osteoclasts from these cells was evaluated by tartrate-resistant acid phosphatase (TRAP) staining and resorption pit formation assay. The effects of picroside II on osteoclastogenesis were studied by examining RANKL-induced osteoclast F-actin ring formation and osteoclast bone resorption. Moreover, we explored the mechanisms of these downregulation effects by performed Western blotting and quantitative RT-PCR examination. Results demonstrated picroside II strongly inhibited RANKL-induced osteoclast formation when added during the early stage of BMMs cultures, suggesting that it acts on osteoclast precursors to inhibit RANKL/RANK signaling. Moreover, picroside II markedly decreased the phosphorylation of p38, ERK, JNK, p65, and I-κB degradation, and significantly suppressed c-Fos and nuclear factor of activated T-cells cytoplasmic 1 (NFATc1), both the key transcription factors during osteoclastogenesis. Furthermore, in vivo studies verified the bone protection effects of picroside II. These results collectively suggested that picroside II acted as an anti-resorption agent by blocking osteoclast activation. J. Cell. Biochem. 118: 4479-4486, 2017. © 2017 Wiley Periodicals, Inc.
胡黄连苷II是从天然植物胡黄连种子中分离出的主要成分之一,在传统中药中广泛应用。本研究旨在确定胡黄连苷II对体外核因子-κB配体(RANKL)刺激的破骨细胞分化以及体内脂多糖(LPS)诱导的骨质流失的影响。收集骨髓细胞(BMMs)并用RANKL诱导,然后用几种剂量的胡黄连苷II处理,通过抗酒石酸酸性磷酸酶(TRAP)染色和吸收陷窝形成试验评估这些细胞中破骨细胞的分化。通过检测RANKL诱导的破骨细胞F-肌动蛋白环形成和破骨细胞骨吸收,研究胡黄连苷II对破骨细胞生成的影响。此外,我们通过蛋白质免疫印迹法和定量逆转录-聚合酶链反应检测来探索这些下调作用的机制。结果表明,在BMMs培养早期添加胡黄连苷II时,它能强烈抑制RANKL诱导的破骨细胞形成,这表明它作用于破骨细胞前体以抑制RANKL/RANK信号传导。此外,胡黄连苷II显著降低p38、ERK、JNK、p65的磷酸化以及I-κB降解,并显著抑制破骨细胞生成过程中的关键转录因子c-Fos和活化T细胞核因子细胞质1(NFATc1)。此外,体内研究证实了胡黄连苷II的骨保护作用。这些结果共同表明,胡黄连苷II通过阻断破骨细胞活化而作为一种抗吸收剂发挥作用。《细胞生物化学杂志》118: 4479 - 4486, 2017年。© 2017威利期刊公司。