Knowles Helen J, Athanasou Nicholas A
Botnar Research Centre, University of Oxford, Nuffield Orthopaedic Centre, Oxford, UK.
J Pathol. 2009 Jun;218(2):256-64. doi: 10.1002/path.2534.
Osteoclasts are the primary mediators of pathological bone resorption in many conditions in which micro-environmental hypoxia is associated with disease progression. However, effects of hypoxia on human osteoclast activity have not been reported. Mature human osteoclasts were differentiated from peripheral blood or obtained from giant cell tumour of bone. Osteoclasts were exposed to a constant hypoxic environment and then assessed for parameters including resorption (toluidine blue staining of dentine slices), membrane integrity (trypan blue exclusion), apoptosis (TUNEL, DAPI), and osteolysis-associated enzyme activity (TRAP, cathepsin K). 24 h exposure to 2% O(2) produced a 2.5-fold increase in resorption associated with increased TRAP and cathepsin K enzyme activity. Hypoxia-Inducible Factor-1alpha (HIF-1alpha) siRNA completely ablated the hypoxic increase in osteoclast resorption. 24 h at 2% O(2) also increased the number of osteoclasts with compromised membrane integrity from 6% to 21%, with no change in the total osteoclast number or the proportion of late-stage apoptotic cells. Transient reoxygenation returned the percentage of trypan blue-positive cells to normoxic levels, suggesting that osteoclasts can recover from the early stages of cell death. Repeated over an extended period, hypoxia/reoxygenation enhanced osteoclast differentiation at this pO(2). These data suggest that in diseased bone, where the pO(2) may fall to <or=2% O(2), a delicate balance between hypoxia-induced osteoclast activation and hypoxia-induced osteoclast apoptosis mediates pathological bone resorption.
破骨细胞是许多疾病中病理性骨吸收的主要介质,在这些疾病中,微环境缺氧与疾病进展相关。然而,缺氧对人破骨细胞活性的影响尚未见报道。成熟的人破骨细胞从外周血中分化而来或取自骨巨细胞瘤。将破骨细胞暴露于恒定的低氧环境中,然后评估包括吸收(牙本质切片的甲苯胺蓝染色)、膜完整性(台盼蓝排斥试验)、凋亡(TUNEL、DAPI)和骨溶解相关酶活性(TRAP、组织蛋白酶K)等参数。暴露于2%氧气24小时后,吸收增加了2.5倍,同时TRAP和组织蛋白酶K酶活性增加。缺氧诱导因子-1α(HIF-1α)小干扰RNA完全消除了破骨细胞吸收的缺氧性增加。在2%氧气环境下24小时也使膜完整性受损的破骨细胞数量从6%增加到21%,破骨细胞总数或晚期凋亡细胞比例没有变化。短暂复氧使台盼蓝阳性细胞百分比恢复到常氧水平,表明破骨细胞可从细胞死亡早期恢复。在这个氧分压下,长时间反复进行缺氧/复氧可增强破骨细胞分化。这些数据表明,在患病骨中,氧分压可能降至≤2%氧气,缺氧诱导的破骨细胞活化与缺氧诱导的破骨细胞凋亡之间的微妙平衡介导了病理性骨吸收。