Shigeyama Y, D'Errico J A, Stone R, Somerman M J
Department of Periodontics/Prevention/Geriatrics, University of Michigan, Ann Arbor, USA.
J Periodontol. 1995 Jun;66(6):478-87. doi: 10.1902/jop.1995.66.6.478.
The well-established finding that implantation of demineralized bone matrix at non-skeletal sites results in formation of cartilage and bone has been attributed to bone morphogenetic proteins/factors. Commercially-available demineralized bone allograft materials are being used currently to reconstruct/regenerate bone. The studies described here focused on establishing biological activity of protein extracts prepared from commercially obtained bone graft material in vitro. Furthermore, the biological activity of these protein extracts in vitro was compared with similar extracts prepared from freshly obtained human bone. Biological activities of bone matrix proteins examined included their ability to promote proliferation, attachment, and migration of gingival fibroblasts using an in vitro system. Guanidine followed by guanidine/EDTA was used to separate bone matrix proteins into proteins associated with soft tissues of bone and proteins retained within the mineral compartment, respectively. Two preparations of each starting material were tested and the biological activity of each preparation was evaluated in triplicate at least three times. Slot blot analysis revealed that commercially-prepared material contained type I collagen; fibronectin; BSP; and BMP-2, 4, and 7. However, the freshly prepared bone extracts appeared to have higher BMP concentrations. The ability of commercial extracts to promote cell proliferation, while significant, was limited and significantly less when compared with similar extracts prepared from freshly obtained bone. All extracts promoted cell attachment significantly, while none of the extracts promoted cell migration. Thus, commercially-prepared material retained proteins having the capacity to influence cell behavior in vivo. However, some biological activity as measured in vitro was lost as a result of tissue processing.
在非骨骼部位植入脱矿骨基质会导致软骨和骨形成,这一已被充分证实的发现归因于骨形态发生蛋白/因子。目前,市售的脱矿骨同种异体移植材料正被用于骨的重建/再生。本文所述研究聚焦于确定从市售骨移植材料制备的蛋白质提取物在体外的生物活性。此外,还将这些蛋白质提取物在体外的生物活性与从新鲜获取的人骨制备的类似提取物进行了比较。所检测的骨基质蛋白的生物活性包括其在体外系统中促进牙龈成纤维细胞增殖、附着和迁移的能力。分别使用胍和胍/乙二胺四乙酸将骨基质蛋白分离为与骨软组织相关的蛋白质和保留在矿物质部分的蛋白质。对每种起始材料的两种制剂进行了测试,每种制剂的生物活性至少进行了三次重复评估。狭缝印迹分析显示,市售材料含有I型胶原蛋白、纤连蛋白、骨涎蛋白以及骨形态发生蛋白-2、-4和-7。然而,新鲜制备的骨提取物似乎具有更高的骨形态发生蛋白浓度。市售提取物促进细胞增殖的能力虽然显著,但有限,与从新鲜获取的骨制备的类似提取物相比明显较低。所有提取物均显著促进细胞附着,但没有一种提取物促进细胞迁移。因此,市售材料保留了具有影响体内细胞行为能力的蛋白质。然而,由于组织处理,一些在体外测量的生物活性丧失了。