Kanda-Nakamura C, Izumi Y, Sueda T
Department of Periodontology, Kagoshima University Dental School, Japan.
J Periodontol. 1996 Dec;67(12):1267-73. doi: 10.1902/jop.1996.67.12.1267.
We investigated the expression of interleukin-1 receptors (IL-1R) on the surfaces of cultured gingival fibroblasts derived from healthy and inflamed gingiva and the effects of IL-1 alpha and IL-1 beta and prostaglandin E2 (PGE2) on IL-1R expression. Fibroblasts were obtained from explant culture of both healthy and inflamed gingiva. IL-1R on cell surfaces was detected immunohistochemically using an anti-human IL-1R monoclonal antibody. IL-1R expression was assessed quantitatively using an enzyme linked immunosorbent assay (ELISA). Positive staining for IL-1R was more evident on cells from inflamed gingiva compared with cells from healthy gingiva. The ELISA showed a significantly increased number of IL-1R on cells from inflamed gingiva compared with cells from healthy gingiva (P < 0.05). Treatment with IL-1 but not PGE2 increased expression of IL-1R on fibroblasts. These findings suggest that gingival fibroblast responses to IL-1 may represent a mechanism for amplification of gingival inflammation.
我们研究了源自健康和发炎牙龈的培养牙龈成纤维细胞表面白细胞介素-1受体(IL-1R)的表达,以及IL-1α、IL-1β和前列腺素E2(PGE2)对IL-1R表达的影响。成纤维细胞取自健康和发炎牙龈的外植体培养物。使用抗人IL-1R单克隆抗体通过免疫组织化学检测细胞表面的IL-1R。使用酶联免疫吸附测定(ELISA)定量评估IL-1R表达。与来自健康牙龈的细胞相比,IL-1R的阳性染色在来自发炎牙龈的细胞上更明显。ELISA显示,与来自健康牙龈的细胞相比,来自发炎牙龈的细胞上IL-1R的数量显著增加(P < 0.05)。用IL-1而非PGE2处理可增加成纤维细胞上IL-1R的表达。这些发现表明,牙龈成纤维细胞对IL-1的反应可能代表了牙龈炎症放大的一种机制。