Neutzsky-Wulff Anita Vibsig, Karsdal Morten A, Henriksen Kim
Nordic Bioscience A/S, Herlev Hovedgade 207, 2730, Herlev, Denmark.
Calcif Tissue Int. 2008 Dec;83(6):425-37. doi: 10.1007/s00223-008-9185-7. Epub 2008 Oct 29.
Mice deficient in the chloride channel ClC-7, which is likely involved in acidification of the resorption lacuna, display severe osteopetrosis. To fully characterize the osteopetrotic phenotype, the phenotypes of osteoclasts and osteoblasts were evaluated. ClC-7(-/-) mice and their corresponding wild-type littermates were killed at 4-5 weeks of age. Biochemical markers of bone resorption (CTX-I), osteoclast number (TRAP5b), and osteoblast activity (ALP) were evaluated in serum. Splenocytes were differentiated into osteoclasts using M-CSF and RANKL. Mature osteoclasts were seeded on calcified or decalcified bone slices, and CTX-I, Ca(2+), and TRAP were measured. Acidification rates in membrane vesicles from bone cells were measured using acridine orange. Osteoblastogenesis and nodule formation in vitro were investigated using calvarial osteoblasts. ClC-7(-/-) osteoclasts were unable to resorb calcified bone in vitro. However, osteoclasts were able to degrade decalcified bone. Acid influx in bone membrane vesicles was reduced by 70% in ClC-7(-/-) mice. Serum ALP was increased by 30% and TRAP5b was increased by 250% in ClC-7(-/-) mice, whereas the CTX/TRAP5b ratio was reduced to 50% of the wild-type level. Finally, evaluation of calvarial ClC-7(-/-) osteoblasts showed normal osteoblastogenesis. In summary, we present evidence supporting a pivotal role for ClC-7 in acidification of the resorption lacuna and evidence indicating that bone formation and bone resorption are no longer balanced in ClC-7(-/-) mice.
缺乏氯离子通道ClC - 7(可能参与吸收陷窝的酸化过程)的小鼠表现出严重的骨硬化。为了全面描述骨硬化表型,对破骨细胞和成骨细胞的表型进行了评估。ClC - 7(-/-)小鼠及其相应的野生型同窝小鼠在4 - 5周龄时处死。检测血清中骨吸收的生化标志物(CTX - I)、破骨细胞数量(TRAP5b)和成骨细胞活性(ALP)。使用M - CSF和RANKL将脾细胞分化为破骨细胞。将成熟破骨细胞接种在钙化或脱钙的骨切片上,检测CTX - I、Ca(2+)和TRAP。使用吖啶橙测量骨细胞膜囊泡中的酸化率。使用颅骨成骨细胞研究体外成骨和结节形成。ClC - 7(-/-)破骨细胞在体外无法吸收钙化骨。然而,破骨细胞能够降解脱钙骨。ClC - 7(-/-)小鼠骨细胞膜囊泡中的酸内流减少了70%。ClC - 7(-/-)小鼠血清ALP增加了30%,TRAP5b增加了250%,而CTX/TRAP5b比值降至野生型水平的50%。最后,对颅骨ClC - 7(-/-)成骨细胞的评估显示成骨正常。总之,我们提供的证据支持ClC - 7在吸收陷窝酸化中起关键作用,并且表明在ClC - 7(-/-)小鼠中骨形成和骨吸收不再平衡。