Department of Oral Surgery, School of Dentistry, Medical University of Vienna, Vienna, Austria.
Core Facility Hard Tissue and Biomaterial Research, Karl Donath Laboratory, School of Dentistry, Medical University of Vienna, Vienna, Austria.
Clin Oral Implants Res. 2018 Apr;29(4):381-388. doi: 10.1111/clr.13133. Epub 2018 Feb 16.
Collagen membranes are not limited to be occlusive barriers as they actively support bone regeneration. However, the impact of bone-derived growth factors on their osteoconductive competence has not been examined.
Twenty adult Sprague Dawley rats were included in the study. Calvaria defects with a diameter of five millimeter were created. The defect was covered with one layer of a collagen membrane previously soaked in conditioned medium of porcine bone chips or in culture medium alone. After 4 weeks, microcomputed tomography was performed. Undecalcified thin-ground sections were subjected to light and scanning electron microscopy. Primary outcome parameter was the bone volume in the defect. Unit of analysis was the bone-conditioned medium (BCM).
In the central defect area of the control and the BCM group, median new bone connected to the host bone was 0.54 and 0.32 mm³, respectively (p = .10). In the ectocranial defect area, the control group showed significantly more bone than the BCM group (0.90 and 0.26 mm³; p = .02). Based on an exploratory interpretation, the control group had smaller bony islands than the BCM group. Scanning electron microscopy and histology indicate the formation of bone but also the collagen membrane to be mineralized in the defect site.
These results demonstrate that the commercial collagen membrane holds an osteoconductive competence in a rat calvaria defect model. Soaking collagen membranes with BCM shifts bone formation toward the formation of bony islands rather than new bone connected to the host bone.
胶原蛋白膜不仅可以作为封闭屏障,还可以积极促进骨再生。然而,骨源性生长因子对其成骨能力的影响尚未得到检验。
本研究纳入了 20 只成年 Sprague Dawley 大鼠。制备直径为 5 毫米的颅骨缺损。用一层先前浸泡在猪骨屑条件培养基或单独培养基中的胶原蛋白膜覆盖缺损。4 周后,进行微计算机断层扫描。对未经脱钙的薄磨片进行光镜和扫描电镜检查。主要观察参数是缺损中的骨体积。分析单位为骨条件培养基(BCM)。
在对照组和 BCM 组的中央缺损区,中位数与宿主骨相连的新骨分别为 0.54 和 0.32 毫米³(p=0.10)。在颅外缺损区,对照组的骨量明显多于 BCM 组(0.90 和 0.26 毫米³;p=0.02)。根据探索性解释,对照组的骨岛比 BCM 组小。扫描电镜和组织学表明,在缺损部位形成了骨,同时胶原蛋白膜也矿化了。
这些结果表明,商业胶原蛋白膜在大鼠颅骨缺损模型中具有成骨能力。用 BCM 浸泡胶原蛋白膜会促使骨形成向骨岛形成转变,而不是与宿主骨相连的新骨形成。