Asotra S, Gupta A K, Sodek J, Aubin J E, Heersche J N
MRC Group in Periodontal Physiology, Faculty of Dentistry, University of Toronto, Ontario, Canada.
J Bone Miner Res. 1994 Jul;9(7):1115-22. doi: 10.1002/jbmr.5650090720.
Rabbit osteoclasts can be transformed from a nonresorbing state to a resorbing state by transferring them from culture medium at pH 7.5 to one at pH 6.5. We evaluated whether expression of mRNA for carbonic anhydrase (CA-II) could be used as an indicator of the state of activity of individual osteoclasts. A cDNA probe to rabbit carbonic anhydrase II (CA-II) was prepared and used for in situ hybridization analysis of osteoclasts isolated from neonatal rabbit long bones. Quantitation by grain counting revealed heterogeneity within the osteoclast population: osteoclasts with a "compact" (rounded, less spread) morphology expressed higher levels of CA-II mRNA than "spread" osteoclasts with similar numbers of nuclei. When maintained at pH 6.5 for 6 h, the level of CA-II mRNA was increased significantly in osteoclasts of both morphologies compared with those in parallel cultures maintained at pH 7.5. These results were confirmed by quantitating CA-II mRNA using the polymerase chain reaction (PCR). Oligonucleotide primers specific for rabbit CA-II were synthesized and used to amplify CA-II cDNA transcribed from mRNA prepared from single or small numbers (one to eight cells) of osteoclasts that were collected with a micromanipulator. This generated a approximately 510 bp PCR product, corresponding to the predicted size of the CA-II fragment encompassed by the primers. For quantitation, CA-II mRNA levels were compared with the levels of a approximately 900 bp actin fragment that was coamplified in the same reaction mixture or amplified separately in a duplicate sample of the reaction mixture.(ABSTRACT TRUNCATED AT 250 WORDS)
通过将兔破骨细胞从pH 7.5的培养基转移至pH 6.5的培养基,可使其从非吸收状态转变为吸收状态。我们评估了碳酸酐酶(CA-II)的mRNA表达是否可作为单个破骨细胞活性状态的指标。制备了兔碳酸酐酶II(CA-II)的cDNA探针,并用于对从新生兔长骨分离的破骨细胞进行原位杂交分析。通过颗粒计数进行定量分析,结果显示破骨细胞群体存在异质性:具有“致密”(圆形、伸展较少)形态的破骨细胞比具有相似核数的“伸展”破骨细胞表达更高水平的CA-II mRNA。当在pH 6.5下维持6小时时,与在pH 7.5下维持的平行培养物相比,两种形态的破骨细胞中CA-II mRNA水平均显著增加。使用聚合酶链反应(PCR)对CA-II mRNA进行定量分析,证实了这些结果。合成了对兔CA-II特异的寡核苷酸引物,并用于扩增从用显微操作器收集的单个或少量(1至8个细胞)破骨细胞制备的mRNA转录的CA-II cDNA。这产生了一个约510 bp的PCR产物,与引物所涵盖的CA-II片段的预测大小相对应。为了进行定量分析,将CA-II mRNA水平与在同一反应混合物中共同扩增或在反应混合物的重复样品中单独扩增的约900 bp肌动蛋白片段的水平进行比较。(摘要截短于250字)