Schaller S, Henriksen K, Sørensen M G, Karsdal M A
Nordic Bioscience A/S, Herlev, Denmark.
Drug News Perspect. 2005 Oct;18(8):489-95. doi: 10.1358/dnp.2005.18.8.944546.
Chloride ions play a major role in osteoclast biology and bone homeostasis. In addition to its general cellular roles, chloride is involved in the specific bone resorption activity of osteoclasts. The chloride channel ClC-7 has been shown to be mandatory for bone resorption. It is necessary for the acidification of the resorption lacunae. In addition to ClC-7, other chloride channels and exchangers have been identified in osteoclasts. The bicarbonate-chloride exchanger at the plasma membrane of osteoclasts is important for regulating the cytoplasmic pH during bone resorption. The role of the additional chloride channels or putative chloride channels identified in osteoclasts, volume-regulated anion channel, Chlor.62 and CLIC1 has not been established. To date, ClC-7 is the only known chloride channel whose disruption or mutation leads to a bone disease: osteopetrosis, which is characterized by an increased bone mass. Inhibition of ClC-7 constitutes a new potential way to treat osteoporosis. The expression of ClC-7 is restricted to few tissues with very high expression in the osteoclasts in bone. Pharmacologically, inhibitors of acidification of the resorption lacunae have proved to be unique, as inhibition leads to a decrease in bone resorption without affecting bone formation, suggesting that the coupling principle has been challenged. Thus, ClC-7 inhibitors may prove to be potent for prevention and treatment of osteoporosis.
氯离子在破骨细胞生物学和骨稳态中发挥着重要作用。除了其在细胞中的一般作用外,氯离子还参与破骨细胞的特异性骨吸收活动。氯离子通道ClC-7已被证明对骨吸收是必不可少的。它对于吸收陷窝的酸化是必要的。除了ClC-7,在破骨细胞中还鉴定出了其他氯离子通道和交换体。破骨细胞质膜上的碳酸氢根-氯离子交换体对于骨吸收过程中调节细胞质pH值很重要。在破骨细胞中鉴定出的其他氯离子通道或假定的氯离子通道,即容积调节性阴离子通道、Chlor.62和CLIC1的作用尚未确定。迄今为止,ClC-7是唯一已知的其破坏或突变会导致一种骨病——骨质石化的氯离子通道,骨质石化的特征是骨量增加。抑制ClC-7构成了一种治疗骨质疏松症的新潜在方法。ClC-7的表达仅限于少数组织,在骨中的破骨细胞中表达非常高。在药理学上,吸收陷窝酸化抑制剂已被证明是独特的,因为抑制会导致骨吸收减少而不影响骨形成,这表明耦合原理受到了挑战。因此,ClC-7抑制剂可能被证明对预防和治疗骨质疏松症有效。