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Zoledronic Acid Is Not Equally Potent on Osteoclasts Generated From Different Individuals

机译:唑醇酸在不同个体产生的破骨细胞上同样有效

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Zoledronic acid is a bisphosphonate commonly used to treat bone diseases such as osteoporosis and cancer‐induced bone disease. Patients exhibit a variable sensitivity to zoledronic acid; the underlying explanation for this remains unclear. The objective of this study was to obtain more knowledge in this regard. We hypothesized that osteoclasts generated from different individuals would show a variable sensitivity to zoledronic acid in vitro. Osteoclasts were generated using monocytes from 46 healthy female blood donors (40 to 66?years). Matured osteoclasts were reseeded onto bone slices precoated with different concentrations of zoledronic acid. IC50 values were determined based on total eroded bone surface after 3?days of resorption. The IC50 for inhibition of osteoclastic bone resorption varied from 0.06 to 12.57μM zoledronic acid; thus, a more than 200‐fold difference in sensitivity to zoledronic acid among osteoclasts from different individuals was observed. Multiple linear regression analyses showed that the determined IC50 correlated with smoking status, and the average number of nuclei per osteoclast in vitro. Further analyses showed that: (i) increasing protein levels of mature cathepsin K in osteoclast cultures rendered the osteoclasts less sensitive to zoledronic acid; (ii) surprisingly, neither the gene nor the protein expression of farnesyl diphosphate synthase was found to correlate with the IC50; and (iii) trench‐forming osteoclasts were found to be more sensitive to zoledronic acid than pit‐forming osteoclasts within the same cell culture. Thus, we conclude that there indeed is a high degree of variation in the potency of zoledronic acid on osteoclasts when generated from different individuals. We propose that our findings can explain some of the varying clinical efficacy of zoledronic acid therapy observed in patients, and may therefore be of clinical importance, which should be investigated in a clinical trial combining in vitro and in vivo investigations. ? 2020 The Authors. JBMR Plus published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research.
机译:唑醇是一种双膦酸盐,通常用于治疗骨质疾病,如骨质疏松症和癌症诱导的骨病。患者对唑醇酸的可变敏感性;对此的根本解释仍然不明确。本研究的目的是在这方面获得更多知识。我们假设从不同个体产生的破骨细胞将在体外显示对唑代酸的可变敏感性。使用来自46个健康女性献血者(40至66岁)的单核细胞产生骨细胞。在含有不同浓度的唑醇酸的骨切片上被重新进入成熟的破骨细胞。 IC 50值基于3.次吸收后的总侵蚀的骨表面测定。用于抑制骨细胞骨吸收的IC50可改变0.06至12.57μm唑醇;因此,观察到来自不同个体的疏松疏松酸的溶血性对来自不同个体的溶血性的敏感性超过200倍。多元线性回归分析表明,确定的IC50与吸烟状态相关,以及体外每骨细胞的平均核数。进一步的分析表明:(i)疏口细胞培养物中成熟组织蛋白酶K的蛋白质水平提高了对唑醇酸的疏松骨细胞溶性敏感性的骨质蛋白酶。 (ii)令人惊讶的是,发现法呢基二磷酸合酶的基因和蛋白质表达与IC50相关; (iii)发现形成沟槽的骨酸粒细胞比在相同细胞培养物内的凹陷骨细胞比坑形成骨细胞更敏感。因此,我们得出结论,当从不同个体产生时,确实存在唑妥酸对疏松骨糖的效力高度变化。我们建议我们的研究结果可以解释患者观察到的唑醇治疗的一些不同的临床疗效,因此可能具有临床重要性,这应该在体外和体内调查中结合的临床试验中进行研究。还是2020作者。 JBMR Plus由Wiley Hearyichs LLC发布代表美国骨骼和矿物学研究。

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