Komiyama K, Hirsch H Z, Moro I, Umemura S, Mestecky J
Department of Microbiology, University of Alabama, Birmingham 35294.
J Oral Pathol. 1988 Mar;17(3):118-23. doi: 10.1111/j.1600-0714.1988.tb01897.x.
The presence of HNK-1 (Leu-7)-positive cells and natural killer (NK) cell activity was determined in human periodontal tissues. Gingival tissues obtained from 25 adult patients were processed for analysis utilizing a HNK-1 (Leu-7) mouse monoclonal antibody. A subpopulation of non-adherent lymphoid cells obtained by collagenase digestion of inflamed gingival tissues from 10 patients was examined for the presence of large granular lymphocytes (LGL) by May-Grünwald-Giemsa staining and for NK cell activity against K562 cells by a 51Cr release cytotoxicity assay. HNK-1+ cells were identified in gingival tissue sections of 21 patients, and were present in or close to discrete foci of plasma cells. HNK-1+ cells were scarce in mildly inflamed or uninflamed tissues sections. LGL were identified in 9 of 10 gingival single-cell suspensions and constituted approximately 5% of the gingival cell population. NK cell-mediated cytolysis, at varying effector/target cell ratios, was observed for 3 of 4 enriched gingival mononuclear cell populations. Gamma-interferon (INF-gamma) preincubation of enriched gingival effector cells from 5 additional patients resulted in a 43% increase in NK cell activity. The finding of increased HNK-1+ cells with gingival inflammation suggests that these cells may play a role in tissue damage, as well as in modulation of B cell activity, in gingivae of patients with periodontal disease.
在人类牙周组织中测定了HNK-1(Leu-7)阳性细胞的存在及自然杀伤(NK)细胞活性。从25名成年患者获取的牙龈组织,利用HNK-1(Leu-7)小鼠单克隆抗体进行处理以用于分析。对10名患者发炎牙龈组织经胶原酶消化获得的非贴壁淋巴细胞亚群,通过May-Grünwald-Giemsa染色检查大颗粒淋巴细胞(LGL)的存在情况,并通过51Cr释放细胞毒性试验检测其对K562细胞的NK细胞活性。在21名患者的牙龈组织切片中鉴定出HNK-1+细胞,且这些细胞存在于浆细胞离散灶中或其附近。在轻度发炎或未发炎的组织切片中,HNK-1+细胞稀少。在10个牙龈单细胞悬液中的9个中鉴定出LGL,其约占牙龈细胞群体的5%。在4个富集的牙龈单核细胞群体中的3个中,观察到了不同效应细胞/靶细胞比例下NK细胞介导的细胞溶解作用。对另外5名患者富集的牙龈效应细胞进行γ-干扰素(INF-γ)预孵育后,NK细胞活性增加了43%。HNK-1+细胞随牙龈炎症增加这一发现表明,这些细胞可能在牙周病患者牙龈的组织损伤以及B细胞活性调节中发挥作用。