Kneser U, Stangenberg L, Ohnolz J, Buettner O, Stern-Straeter J, Möbest D, Horch R E, Stark G B, Schaefer D J
Department of Plastic and Hand Surgery, University of Erlangen Medical Center, Erlangen, Germany.
J Cell Mol Med. 2006 Jul-Sep;10(3):695-707. doi: 10.1111/j.1582-4934.2006.tb00429.x.
Biologic bone substitutes may offer alternatives to bone grafting procedures. The aim of this study was to evaluate a preformed bone substitute based on processed bovine cancellous bone (PBCB) with or without osteogenic cells in a critical size calvarial defect rat model.
Discs of PBCB (Tutobone) were seeded with second passage fibrin gel-immobilized syngenic osteoblasts (group A, n = 40). Cell-free matrices (group B, n = 28) and untreated defects (group C; n=28) served as controls. Specimens were explanted between day 0 and 4 months after implantation and were subjected to histological and morphometric evaluation.
At 1 month, bone formation was limited to small peripheral areas. At 2 and 4 months, significant bone formation, matrix resorption as well as integration of the implants was evident in groups A and B. In group C no significant regeneration of the defects was observed. Morphometric analysis did not disclose differences in bone formation in matrices from groups A and B. Carboxyfluorescine-Diacetate-Succinimidylester (CFDA) labeling demonstrated low survival rates of transplanted cells.
Osteoblasts seeded into PBCB matrix display a differentiated phenotype following a 14 days cell culture period. Lack of initial vascularization may explain the absence of added osteogenicity in constructs from group A in comparison to group B. PBCB is well integrated and represents even without osteogenic cells a promising biomaterial for reconstruction of critical size calvarial bone defects.
生物骨替代物可能为骨移植手术提供替代方案。本研究的目的是在大鼠颅骨临界尺寸缺损模型中评估一种基于处理过的牛松质骨(PBCB)的预制骨替代物,该替代物添加或未添加成骨细胞。
将第二代纤维蛋白凝胶固定的同基因成骨细胞接种到PBCB(Tutobone)圆盘上(A组,n = 40)。无细胞基质(B组,n = 28)和未处理的缺损(C组,n = 28)作为对照。在植入后0至4个月之间取出标本,进行组织学和形态计量学评估。
1个月时,骨形成仅限于小的周边区域。在2个月和4个月时,A组和B组均有明显的骨形成、基质吸收以及植入物整合。C组未观察到缺损的明显再生。形态计量学分析未发现A组和B组基质中骨形成的差异。羧基荧光素二乙酸琥珀酰亚胺酯(CFDA)标记显示移植细胞的存活率较低。
接种到PBCB基质中的成骨细胞在14天的细胞培养期后表现出分化的表型。与B组相比,A组构建体中缺乏初始血管化可能解释了其额外成骨作用不足的原因。PBCB整合良好,即使没有成骨细胞,也是用于重建颅骨临界尺寸骨缺损的一种有前景的生物材料。