Makihira Seicho, Mine Yuichi, Kosaka Eduardo, Nikawa Hiroki
Department of Medical Design and Engineering, Division of Oral Health Engineering, Institute for Oral Health Science, Hiroshima University Faculty of Dentistry, 1-2-3 Kasumi Minami-ku, Hiroshima 734-8553, Japan.
Dent Mater J. 2007 Sep;26(5):739-45. doi: 10.4012/dmj.26.739.
The present study was a molecular analysis of the initial differentiation of osteoclast precursor RAW264.7 cells on titanium specimens. RAW264.7 cell line was cultured on titanium specimens of which the surfaces were finished by wet grinding with 2000-, 1200-, 600-, or 180-grit waterproof abrasive paper. Total RNA was extracted from cells cultured in the presence or absence of Receptor Activator of NF-kappaB Ligand (RANKL), prior to cDNA synthesis for real-time quantitative reverse transcriptase-polymerase chain reaction analysis. Titanium surfaces initially enhanced the expression of osteoclast differentiation markers including tartrate-resistant acid phosphatase and cathepsin K in RAW264.7 cells cultured with RANKL stimulation, in a roughness-dependent manner. The mRNA expressions of both RANKL receptor, RANK, and its adapter protein TNF receptor-associated factor 6 (TRAF6) increased when RAW264.7 cells were cultured on titanium specimens with roughened surfaces, as compared with that of control specimen with a polished surface. These results, taken together, suggested that titanium surface roughness facilitated osteoclast differentiation through the activation of the RANK-TRAF6 signaling network.
本研究是对破骨细胞前体RAW264.7细胞在钛标本上初始分化的分子分析。RAW264.7细胞系培养在钛标本上,这些标本的表面用2000目、1200目、600目或180目的防水砂纸进行湿磨处理。在进行实时定量逆转录聚合酶链反应分析的cDNA合成之前,从在有或无核因子κB受体激活配体(RANKL)的情况下培养的细胞中提取总RNA。在RANKL刺激下培养的RAW264.7细胞中,钛表面最初以粗糙度依赖的方式增强了破骨细胞分化标志物(包括抗酒石酸酸性磷酸酶和组织蛋白酶K)的表达。与具有抛光表面的对照标本相比,当RAW264.7细胞培养在具有粗糙表面的钛标本上时,RANKL受体RANK及其衔接蛋白肿瘤坏死因子受体相关因子6(TRAF6)的mRNA表达均增加。综上所述,这些结果表明钛表面粗糙度通过激活RANK-TRAF6信号网络促进破骨细胞分化。