Knabe Christine, Nicklin Sean, Yu Yan, Walsh William R, Radlanski Ralf J, Marks Christian, Hoffmeister Bodo
Department of Experimental Dentistry, Charité - University Medical Centre Berlin, Campus Benjamin Franklin, Germany.
J Craniomaxillofac Surg. 2005 Dec;33(6):361-9. doi: 10.1016/j.jcms.2005.07.003. Epub 2005 Oct 25.
Lengthening the mandible by distraction osteogenesis (DO) is nowadays a well recognized technique in maxillofacial surgery. In this study growth factor expression profiles were examined in biopsies taken from six patients undergoing mandibular DO and compared with findings from a sheep model for mandibular DO.
In all patients (and sheep), the ascending ramus was distracted 10-15 mm at a rate of 1mm/day using an intraoral device. Biopsies were taken from the centre of the distraction zone 21 days after completion of distraction. Using standard immunohistochemical techniques, samples were stained for platelet-derived growth factor (PDGF), transforming growth factor beta (TGF-beta), basic fibroblast growth factor (bFGF) and bone morphogenetic proteins-2, -4 and -7 (BMP-2, -4, -7), matrix metalloproteinases-1 and -3 (MMP-1, -3), the vascular endothelial growth factor (VEGF), a marker for endothelial cells (CD-31) and type IV collagen (Col IV).
Positive staining for PDGF, bFGF, TGF-beta, BMP-2, -4, and -7 was noted in cells and matrix components. There was intense staining for MMP-1. Strong staining for CD-31 and COL IV was observed adjacent to vessels. VEGF staining was less specific. Similar findings were noted in the sheep model.
Growth factor expression in the human distraction site is similar to that in the sheep model.
通过牵张成骨术(DO)延长下颌骨如今在颌面外科中是一种公认的技术。在本研究中,对6例行下颌骨DO患者的活检组织进行生长因子表达谱检测,并与下颌骨DO绵羊模型的结果进行比较。
在所有患者(和绵羊)中,使用口内装置以每天1毫米的速度将升支牵张10 - 15毫米。牵张完成21天后,从牵张区中心获取活检组织。使用标准免疫组织化学技术,对样本进行血小板衍生生长因子(PDGF)、转化生长因子β(TGF-β)、碱性成纤维细胞生长因子(bFGF)以及骨形态发生蛋白-2、-4和-7(BMP-2、-4、-7)、基质金属蛋白酶-1和-3(MMP-1、-3)、血管内皮生长因子(VEGF)、内皮细胞标志物(CD-31)和IV型胶原(Col IV)染色。
在细胞和基质成分中发现PDGF、bFGF、TGF-β、BMP-2、-4和-7呈阳性染色。MMP-1染色强烈。在血管附近观察到CD-31和COL IV染色较强。VEGF染色特异性较低。在绵羊模型中也观察到类似结果。
人类牵张部位的生长因子表达与绵羊模型相似。