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Alterations in osteoclast function and phenotype induced by different inhibitors of bone resorption - implications for osteoclast quality

破骨细胞 骨吸收 吸收 内分泌学 内科学 双膦酸盐 组织蛋白酶K 组织蛋白酶 兰克尔 骨重建 骨质疏松症 医学 化学 生物化学 受体 激活剂(遗传学)
作者
A.V. Neutzsky-Wulff,Mette G Sørensen,Dino Kocijancic,Diana Julie Leeming,Morten Hanefeld Dziegiel,M.A. Karsdal,Kim Henriksen
出处
期刊:BMC Musculoskeletal Disorders [BioMed Central]
卷期号:11 (1): 109-109 被引量:18
标识
DOI:10.1186/1471-2474-11-109
摘要

Abstract Background Normal osteoclasts resorb bone by secretion of acid and proteases. Recent studies of patients with loss of function mutations affecting either of these processes have indicated a divergence in osteoclastic phenotypes. These difference in osteoclast phenotypes may directly or indirectly have secondary effects on bone remodeling, a process which is of importance for the pathogenesis of both osteoporosis and osteoarthritis. We treated human osteoclasts with different inhibitors and characterized their resulting function. Methods Human CD14 + monocytes were differentiated into mature osteoclasts using RANKL and M-CSF. The osteoclasts were cultured on bone in the presence or absence of various inhibitors: Inhibitors of acidification (bafilomycin A1, diphyllin, ethoxyzolamide), inhibitors of proteolysis (E64, GM6001), or a bisphosphonate (ibandronate). Osteoclast numbers and bone resorption were monitored by measurements of TRACP activity, the release of calcium, CTX-I and ICTP, as well as by counting resorption pits. Results All inhibitors of acidification were equally potent with respect to inhibition of both organic and inorganic resorption. In contrast, inhibition of proteolysis by E64 potently reduced organic resorption, but only modestly suppressed inorganic resorption. GM6001 alone did not greatly affect bone resorption. However, when GM6001 and E64 were combined, a complete abrogation of organic bone resorption was observed, without a great effect on inorganic resorption. Ibandronate abrogated both organic and inorganic resorption at all concentrations tested [0.3-100 μM], however, this treatment dramatically reduced TRACP activity. Conclusions We present evidence highlighting important differences with respect to osteoclast function, when comparing the different types of osteoclast inhibitors. Each class of osteoclast inhibitors will lead to different alterations in osteoclast quality, which secondarily may lead to different bone qualities.

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