Laitala T, Väänänen K
Department of Anatomy, University of Oulu, Finland.
J Bone Miner Res. 1993 Jan;8(1):119-26. doi: 10.1002/jbmr.5650080115.
Immobilization causes a transient increase in bone resorption and a prolonged depression of bone formation. We have studied the effect of immobilization on the expression of two proteins believed to have a major functional role in osteoclasts, the proteolipid subunit of vacuolar H(+)-ATPase (VPL) and carbonic anhydrase II (CA II). Trabecular bone from immobilized rat tibiae was analyzed using northern and slot blotting, polymerase chain reaction (PCR), and morphometric analysis. CA II and VPL transcription was rapidly stimulated in trabecular bone of immobilized rat tibiae. Osteoclast number increased and the trabecular bone volume decreased during immobilization. Fluorescein-labeled cDNA probes and a confocal laser scanning microscope were used to study the localization of VPL and CA II mRNAs in situ in osteoclasts and other bone-derived cells attached to bovine bone slices in vitro. CA II and VPL mRNA were highly expressed in actively resorbing osteoclasts, but in nonresorbing osteoclasts mRNA expression was very low or not detectable at all. These results strongly suggest that both CA II and VPL have an important functional role in bone resorption. Finally, in the bone cell population isolated for these studies, CA II was found to be highly specific for osteoclasts whereas VPL was also detected in other cell types.
制动会导致骨吸收短暂增加以及骨形成长期受抑制。我们研究了制动对两种被认为在破骨细胞中起主要功能作用的蛋白质表达的影响,即液泡H(+)-ATP酶的蛋白脂质亚基(VPL)和碳酸酐酶II(CA II)。使用Northern印迹法、狭缝印迹法、聚合酶链反应(PCR)和形态计量分析对制动大鼠胫骨的小梁骨进行了分析。在制动大鼠胫骨的小梁骨中,CA II和VPL转录迅速受到刺激。制动期间破骨细胞数量增加且小梁骨体积减小。使用荧光素标记的cDNA探针和共聚焦激光扫描显微镜研究了VPL和CA II mRNA在体外附着于牛骨切片的破骨细胞和其他骨源性细胞中的原位定位。CA II和VPL mRNA在活跃吸收的破骨细胞中高表达,但在不吸收的破骨细胞中mRNA表达非常低或根本检测不到。这些结果强烈表明CA II和VPL在骨吸收中都具有重要的功能作用。最后,在为这些研究分离的骨细胞群体中,发现CA II对破骨细胞具有高度特异性,而VPL也在其他细胞类型中被检测到。