Collin-Osdoby P, Li L, Rothe L, Anderson F, Kirsch D, Oursler M J, Osdoby P
Department of Biology, Washington University, St. Louis, Missouri 63130, USA.
J Bone Miner Res. 1998 Jan;13(1):67-78. doi: 10.1359/jbmr.1998.13.1.67.
Osteoclasts generate high levels of superoxide anions during bone resorption that contribute to the degradative process, although excessive levels of this free radical may be damaging. One mechanism for their removal is via superoxide dismutase (SOD), a protective superoxide scavenging enzyme. We have previously described a novel developmentally regulated 150 kDa plasma membrane glycoprotein of avian osteoclasts which is reactive with the osteoclast-specific monoclonal antibody (Mab) 121F and is related immunologically, biochemically, and in protein sequence to mitochondrial Mn2+/Fe2+ SOD. We hypothesized that this unusual osteoclast surface component may be involved in protection against superoxides generated during active bone resorption. Increasing concentrations of monovalent Fab fragments prepared from Mab 121F, but not those from another antiosteoclast Mab designated 29C, markedly inhibited both bone particle and bone pit resorption by avian osteoclasts, while reducing tartrate-resistant acid phosphatase activity and causing the morphological contraction of osteoclasts on bone. Thus, the SOD-related membrane antigen may be essential for osteoclast bone resorption. Osteoclast superoxide production, monitored kinetically by cytochrome c reduction and histochemically by nitroblue tetrazolium reduction staining, was significantly greater in the presence of 121F, but not 29C, Fab treatment. Furthermore, the release of another free radical known as nitric oxide, which is produced by osteoclasts, can scavenge superoxides, and acts to potently inhibit osteoclast bone resorption, was dose-dependently increased by 121F Fab in resorbing osteoclast cultures. Therefore, Mab 121F binding may block the potential protective function of the osteoclast plasma membrane SOD-related glycoprotein, leading to a rapid elevation of superoxide levels and a subsequent rise in osteoclast nitric oxide release, feedback messages which may be sensed by the osteoclast as signals to cease active bone resorption.
破骨细胞在骨吸收过程中会产生大量超氧阴离子,这些超氧阴离子有助于降解过程,尽管过量的这种自由基可能具有破坏性。清除它们的一种机制是通过超氧化物歧化酶(SOD),一种具有保护作用的超氧清除酶。我们之前描述过一种新的、在发育过程中受调控的禽破骨细胞150 kDa质膜糖蛋白,它与破骨细胞特异性单克隆抗体(Mab)121F发生反应,并且在免疫、生化和蛋白质序列方面与线粒体Mn2+/Fe2+ SOD相关。我们推测这种不寻常的破骨细胞表面成分可能参与了对活跃骨吸收过程中产生的超氧化物的保护。从Mab 121F制备的单价Fab片段浓度增加时,而非从另一种名为29C的抗破骨细胞Mab制备的Fab片段,能显著抑制禽破骨细胞对骨颗粒和骨陷窝的吸收,同时降低抗酒石酸酸性磷酸酶活性,并导致破骨细胞在骨上的形态收缩。因此,与SOD相关的膜抗原可能对破骨细胞的骨吸收至关重要。通过细胞色素c还原动力学监测以及通过硝基蓝四唑还原染色组织化学监测发现,在121F而非29C的Fab处理下,破骨细胞超氧产生显著增加。此外,破骨细胞产生的另一种自由基一氧化氮的释放可以清除超氧化物,并有力地抑制破骨细胞的骨吸收,在进行骨吸收的破骨细胞培养物中,121F Fab能使一氧化氮的释放呈剂量依赖性增加。因此,Mab 121F的结合可能会阻断破骨细胞质膜上与SOD相关糖蛋白的潜在保护功能,导致超氧水平迅速升高,随后破骨细胞一氧化氮释放增加,这些反馈信息可能被破骨细胞感知为停止活跃骨吸收的信号。