Walsh L J, Seymour G J, Powell R N
J Dent Res. 1986 Dec;65(12):1424-6. doi: 10.1177/00220345860650120901.
T6 is an antigen which is a highly specific marker for Langerhans cells. Previous studies have demonstrated that Interleukin-1 (IL-1) and an IL-1 inhibitor (ILS) modulate T6 expression (T6E) in explant culture. The present study examined the effects of IL-1 and ILS on T6E in dispersed gingival epithelial cell (EC) cultures. EC were obtained by trypsinization of gingival fragments obtained during periodontal surgery. T6E by EC was demonstrated using OKT6 monoclonal antibody in an immuno-peroxidase technique. In both unseparated and T6-depleted EC, IL-1 (0.5 U/mL) stimulated T6E, and this effect was abrogated by ILS (1:30). ILS alone depressed T6E in unseparated EC cultures. All effects were consistent between four- and 24-hour culture periods, and no treatment affected EC viability, thus excluding cell proliferation or necrosis as a vector for the action of IL-1 and ILS. These results indicate that a population of epithelial cells exists which is induced to express T6 under the influence of IL-1. IL-1 and ILS act in combination to regulate T6E on these precursor cells and on DR(-) Langerhans cells in gingival epithelium.
T6是一种抗原,是朗格汉斯细胞的高度特异性标志物。先前的研究表明,白细胞介素-1(IL-1)和一种IL-1抑制剂(ILS)在外植体培养中调节T6表达(T6E)。本研究检测了IL-1和ILS对分散的牙龈上皮细胞(EC)培养物中T6E的影响。通过胰蛋白酶消化在牙周手术期间获得的牙龈碎片来获取EC。在免疫过氧化物酶技术中使用OKT6单克隆抗体来证明EC的T6E。在未分离的和T6耗尽的EC中,IL-1(0.5 U/mL)均刺激T6E,并且这种作用被ILS(1:30)消除。单独使用ILS会降低未分离的EC培养物中的T6E。在4小时和24小时培养期之间所有作用都是一致的,并且没有处理影响EC活力,因此排除了细胞增殖或坏死作为IL-1和ILS作用的载体。这些结果表明存在一群上皮细胞,其在IL-1的影响下被诱导表达T6。IL-1和ILS共同作用以调节这些前体细胞以及牙龈上皮中DR(-)朗格汉斯细胞上的T6E。