Matsuura M, Herr Y, Han K Y, Lin W L, Genco R J, Cho M I
Department of Oral Biology, School of Dental Medicine, State University of New York, Buffalo, USA.
J Periodontol. 1995 Jul;66(7):579-93. doi: 10.1902/jop.1995.66.7.579.
Periodontal regeneration requires formation of periodontal tissues lost due to periodontal disease. To better understand the formation of new periodontal tissues during periodontal repair and regeneration, immunohistochemical expression of extracellular matrix components of normal as well as healing periodontal tissues was evaluated and compared using the avidin-biotin complex immunohistochemical technique. For this purpose, horizontal furcation defects were created around mandibular P2 and P4 of 6 dogs after extraction of P1 and P3. The root surfaces were conditioned with citric acid and expanded polytetrafluoroethylene (ePTFE) membranes were placed and retained 0.5 mm above the cemento-enamel junction. The mucoperiosteal flaps were sutured in a coronal position. Two animals were sacrificed at 2, 4, and 8 weeks, and mesio-distal tissue slices containing normal or healing periodontal tissues were demineralized, dehydrated, and embedded in paraffin. Immunohistochemical localization of type I collagen (CI), fibronectin (FN), secreted protein, acidic and rich in cysteine (SPARC), vitronectin (VN), and bone sialoprotein (BSP) was performed on 6 microns thick sections. Morphological results demonstrated that at 2 weeks after defect creation, lesions were filled primarily with granulation tissue which was gradually replaced by newly-formed fibrous connective tissue, periodontal ligament (PDL), cementum, and bone between 4 and 8 weeks. The results of immunohistochemical study revealed that at 2 weeks the granulation tissue, especially in the intercellular spaces of inflammatory cells, was intensively stained for FN and VN. At 4 and 8 weeks, staining for CI, FN, and VN was found in fibrous connective tissue, the newly-formed PDL, cementum, and osteoid. Further the attachment zone of the PDL collagen fibers to cementum showed intense staining for FN. Immunostaining for SPARC was positive in the new PDL, cementum, and bone, while staining for BSP was restricted to the new cementum and bone. Interestingly, the PDL, especially in areas adjacent to active bone formation, demonstrated intense staining for BSP. However, fibrous connective tissue and PDL proper were unstained for BSP. These results indicate that FN and VN are involved in the early stages of periodontal repair, and periodontal regeneration is achieved through formation of periodontal tissues that are composed of different matrix components specific to different types of periodontal tissues.
牙周组织再生需要形成因牙周病而丧失的牙周组织。为了更好地理解牙周修复和再生过程中新生牙周组织的形成,采用抗生物素蛋白-生物素复合物免疫组织化学技术,对正常及愈合期牙周组织细胞外基质成分的免疫组织化学表达进行了评估和比较。为此,在拔除6只犬的P1和P3后,于下颌P2和P4周围制造水平根分叉病变。用柠檬酸处理牙根表面,并放置扩展聚四氟乙烯(ePTFE)膜,使其在牙骨质-釉质界上方0.5mm处保持在位。将粘骨膜瓣缝合在冠方位置。在2周、4周和8周时处死2只动物,将包含正常或愈合期牙周组织的近远中组织切片进行脱矿、脱水,然后石蜡包埋。在6微米厚的切片上进行I型胶原(CI)、纤连蛋白(FN)、富含半胱氨酸的酸性分泌蛋白(SPARC)、玻连蛋白(VN)和骨唾液蛋白(BSP)的免疫组织化学定位。形态学结果表明,在制造病变后2周,病变主要由肉芽组织填充,在4至8周期间逐渐被新形成的纤维结缔组织、牙周韧带(PDL)、牙骨质和骨替代。免疫组织化学研究结果显示,在2周时,肉芽组织,尤其是炎症细胞的细胞间隙,FN和VN染色强烈。在4周和8周时,在纤维结缔组织、新形成的PDL、牙骨质和类骨质中发现CI、FN和VN染色。此外,PDL胶原纤维与牙骨质的附着区FN染色强烈。SPARC在新的PDL、牙骨质和骨中的免疫染色呈阳性,而BSP的染色仅限于新的牙骨质和骨。有趣的是,PDL,尤其是在与活跃骨形成相邻的区域,BSP染色强烈。然而,纤维结缔组织和固有PDL未被BSP染色。这些结果表明,FN和VN参与牙周修复的早期阶段,并且通过形成由不同类型牙周组织特有的不同基质成分组成的牙周组织来实现牙周组织再生。