Biskobing D M, Fan D
Department of Medicine, Medical College of Virginia at Virginia Commonwealth University, Richmond, USA.
Calcif Tissue Int. 2000 Aug;67(2):178-83. doi: 10.1007/s00223001107.
Numerous resorptive stimuli have been shown to enhance osteoclast differentiation, increasing osteoclast numbers and accelerating bone resorption. Currently, there is much less understanding of regulation of mature osteoclast activity. Indeed, there is presently only minimal evidence of changes in gene expression as a mechanism for altering bone resorption. We investigate here, in the mature osteoclast, regulation of 2 genes-carbonic anhydrase II (CAII) and calcitonin receptor (CTR) in response to acidosis, which is known to increase bone resorption. We studied the effect of acid pH on CAII and CTR mRNA expression in mature osteoclasts raised in coculture of ST-2 and primary marrow cells. On day 6 of culture, stromal cells were removed with collagenase, the remaining osteoclasts were incubated overnight, and then exposed to varying pH. RT-PCR was performed on total RNA using primers for CAII, CTR, or glyceraldehyde dehydrogenase phosphate (GAP). Expression of CTR mRNA was increased 2.14 +/- 0.41 and 2.56 +/- 0.45 (P < 0.05)-fold by a 4-hour exposure to pH 6.75 and 6.5, respectively. CAII mRNA was similarly increased 2.18 +/- 0.42 and 2.63 +/- 0.48 (P < 0.05)-fold by pH 6.75 and 6.5, respectively. Increased expression of CAII and CTR mRNA was seen by 2 hours and maximally by 4 hours. Increased expression of CTR and CAII mRNA was not explained by increases in osteoclast numbers: pH 7.4-100 +/- 3.7, 6.75-133 +/- 8.3, 6.5-124 +/- 7.8. These results demonstrate upregulation of two osteoclast genes in response to acidosis, illustrating the ability of the mature osteoclast to respond to resorptive signals with increased functional gene expression.
大量的吸收性刺激已被证明可增强破骨细胞分化,增加破骨细胞数量并加速骨吸收。目前,对于成熟破骨细胞活性的调节了解较少。事实上,目前仅有极少的证据表明基因表达变化是改变骨吸收的一种机制。我们在此研究成熟破骨细胞中两个基因——碳酸酐酶II(CAII)和降钙素受体(CTR)对酸中毒的反应调节,酸中毒已知会增加骨吸收。我们研究了酸性pH对在ST - 2和原代骨髓细胞共培养中培养的成熟破骨细胞中CAII和CTR mRNA表达的影响。在培养的第6天,用胶原酶去除基质细胞,将剩余的破骨细胞孵育过夜,然后暴露于不同的pH值。使用CAII、CTR或磷酸甘油醛脱氢酶(GAP)的引物对总RNA进行逆转录聚合酶链反应(RT - PCR)。分别在pH 6.75和6.5下暴露4小时后,CTR mRNA的表达分别增加了2.14±0.41倍和2.56±0.45倍(P < 0.05)。CAII mRNA在pH 6.75和6.5下同样分别增加了2.18±0.42倍和2.63±0.48倍(P < 0.05)。在2小时时可见CAII和CTR mRNA表达增加,4小时时达到最大值。CTR和CAII mRNA表达的增加并非由破骨细胞数量增加所解释:pH 7.4时为100±3.7,pH 6.75时为133±8.3,pH 6.5时为124±7.8。这些结果表明,酸中毒可使两个破骨细胞基因上调,说明成熟破骨细胞能够通过增加功能性基因表达来响应吸收信号。