Kennett C N, Cox S W, Eley B M
Department of Periodontology, London Hospital Medical College, UK.
J Periodontol. 1996 Sep;67(9):846-52. doi: 10.1902/jop.1996.67.9.846.
Dipeptidyl peptidase (DPP) II and IV activities were demonstrated in unfixed cryostat sections of gingival tissue from chronic periodontitis patients using histochemistry with 2-methoxy-4-naphthylamine (MNA) substrates. In the case of DPP IV, enzyme localization was confirmed by immunocytochemistry with mouse monoclonal antihuman DPP IV (CD26) antibody. Inflammatory cells containing enzyme were identified in adjacent sections with mouse monoclonal antibodies directed against leukocyte differentiation antigens. Lys-Ala-MNA and Ala-Pro-MNA staining in acid buffer for DPP II was only found in a few fibroblasts in superficial tissue. Staining with Gly-Pro-MNA and Ala-Pro-MNA in alkaline buffer for DPP IV was localized in some CD4 and CD8 positive T lymphocytes, CD68 positive macrophages, and fibroblasts and these cells also reacted with the enzyme antibody. DPP IV-containing macrophages and T lymphocytes were seen in the epithelium. In deeper granulomatous tissue Gram positive and negative bacteria stained with the histochemical substrates, but not the DPP IV antibody. Fibroblast DPP II and IV might participate in cellular interactions with collagen, while T lymphocyte DPP IV may be involved in cell signalling.
使用含2-甲氧基-4-萘胺(MNA)底物的组织化学方法,在慢性牙周炎患者牙龈组织的未固定低温切片中证实了二肽基肽酶(DPP)II和IV的活性。对于DPP IV,通过用小鼠单克隆抗人DPP IV(CD26)抗体进行免疫细胞化学来确认酶的定位。在相邻切片中,用针对白细胞分化抗原的小鼠单克隆抗体鉴定出含有该酶的炎症细胞。用于DPP II的酸性缓冲液中的Lys-Ala-MNA和Ala-Pro-MNA染色仅在表层组织的少数成纤维细胞中发现。用于DPP IV的碱性缓冲液中的Gly-Pro-MNA和Ala-Pro-MNA染色定位于一些CD4和CD8阳性T淋巴细胞、CD68阳性巨噬细胞和成纤维细胞,并且这些细胞也与酶抗体发生反应。在上皮中可见含有DPP IV的巨噬细胞和T淋巴细胞。在更深的肉芽肿组织中,革兰氏阳性和阴性细菌可被组织化学底物染色,但不能被DPP IV抗体染色。成纤维细胞的DPP II和IV可能参与与胶原蛋白的细胞相互作用,而T淋巴细胞的DPP IV可能参与细胞信号传导。