Department of Clinical Pharmacology, Hirosaki University Graduate School of Medicine, Hirosaki 036-8562, Japan.
J Bone Miner Metab. 2009;27(6):653-62. doi: 10.1007/s00774-009-0085-3. Epub 2009 May 19.
Mechanical stress application is a unique method for bone studies. We have reported regulation via the p38 mitogen-activated protein kinase (MAPK) pathway in osteoblasts under application of cyclic tensile strain (CTS), among many reports on the extracellular signal-regulated kinase (ERK) 1/2 pathway during mechanical stress, and questions remain as to the differences between our findings and those of others regarding types of MAPK activation. In the present study, osteoblasts were used after the third passage and stimulated by the application of 7%, 0.25 Hz CTS for 3 days, 4 h/day. CTS-induced osteoprotegerin (OPG) synthesis in osteoblasts increased at the third passage and decreased at the fifth passage, whereas CTS-induced receptor activator of nuclear factor-kappaB ligand (RANKL) mRNA expression decreased in osteoblasts at the third passage and increased at the fifth passage. Increases in CTS-induced osteopontin (OPN) synthesis, cyclooxygenase-2 (Cox-2) mRNA expression, and nitric oxide (NO) production by osteoblasts did not change at the third and fifth passages. Furthermore, p38 MAPK at the third passage and ERK1/2 at the fifth passage were found to be competitively activated in osteoblasts by the application of CTS. Based on these results, osteoblasts were shown to be affected by the number of passages. It was suggested that the examination of passage-affected characteristics of osteoblasts might not only be pertinent to the analysis of cellular senescence and in vivo models of bone remodelling with aging but could also be useful in the development of bone tissue engineering.
机械应力施加是骨研究的独特方法。我们已经报道了在施加循环拉伸应变(CTS)时,成骨细胞中 p38 丝裂原活化蛋白激酶(MAPK)途径的调节,这是许多关于机械应力下细胞外信号调节激酶(ERK)1/2 途径的报告之一,关于 MAPK 激活的我们的发现与其他研究的差异仍存在疑问。在本研究中,使用第三代细胞,每天施加 7%、0.25Hz CTS 刺激 3 天。CTS 诱导第三代成骨细胞中骨保护素(OPG)合成增加,第五代成骨细胞中减少,而 CTS 诱导第三代成骨细胞中核因子-κB 受体激活剂配体(RANKL)mRNA 表达减少,第五代成骨细胞中增加。CTS 诱导第三代成骨细胞中骨桥蛋白(OPN)合成、环氧化酶-2(Cox-2)mRNA 表达和一氧化氮(NO)产生增加,在第三和第五代没有变化。此外,在第三代的 p38 MAPK 和第五代的 ERK1/2 被发现通过 CTS 的应用在成骨细胞中竞争激活。基于这些结果,成骨细胞受到传代数的影响。表明成骨细胞的传代影响特征的检查不仅与细胞衰老的分析和体内骨重塑与衰老模型相关,而且对骨组织工程的发展也可能有用。