Watanabe M, Ueno Y, Yajima T, Iwao Y, Tsuchiya M, Ishikawa H, Aiso S, Hibi T, Ishii H
Department of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.
J Clin Invest. 1995 Jun;95(6):2945-53. doi: 10.1172/JCI118002.
The interaction of mucosal lymphocytes and intestinal epithelial cells is thought to be important in regulating immune response in the intestinal mucosa, but conclusive evidence is limited. Here we demonstrate the expression of IL-7 mRNA in human intestinal mucosa by combined reverse transcription PCR and Southern blot hybridization. Immunohistochemistry and in situ hybridization confirm the presence of IL-7 in intestinal epithelial cells, especially in epithelial goblet cells. Moreover, IL-7 receptor expression in mucosal lymphocytes is demonstrated by immunohistochemistry and in situ hybridization, as well as by Southern blot and flow cytometric analysis of freshly isolated lamina propria lymphocytes. In contrast, IL-7 receptor could not be detected in the cell surface of freshly isolated PBLs. The functional activity of IL-7 receptor is demonstrated by the utility of recombinant IL-7 to stimulate the growth of lamina propria lymphocytes, and conversely inhibit CD3-dependent proliferation of these cells. In contrast, IL-7 caused no significant increase in DNA synthesis and cell numbers when added to PBLs. These findings suggest that human intestinal epithelial cells and epithelial goblet cells produce IL-7, and locally produced IL-7 may serve as a potent regulatory factor for intestinal mucosal lymphocytes.
黏膜淋巴细胞与肠上皮细胞之间的相互作用被认为在调节肠黏膜免疫反应中起重要作用,但确凿证据有限。在此,我们通过逆转录聚合酶链反应(PCR)与Southern印迹杂交相结合的方法,证明了人肠黏膜中白细胞介素-7(IL-7)信使核糖核酸(mRNA)的表达。免疫组织化学和原位杂交证实了IL-7在肠上皮细胞中存在,尤其在上皮杯状细胞中。此外,通过免疫组织化学、原位杂交以及对新鲜分离的固有层淋巴细胞进行Southern印迹和流式细胞术分析,证明了黏膜淋巴细胞中IL-7受体的表达。相比之下,在新鲜分离的外周血淋巴细胞(PBLs)的细胞表面未检测到IL-7受体。重组IL-7可刺激固有层淋巴细胞生长,反之抑制这些细胞依赖CD3的增殖,从而证明了IL-7受体的功能活性。相比之下,将IL-7添加到PBLs中时,DNA合成和细胞数量没有显著增加。这些发现表明,人肠上皮细胞和上皮杯状细胞产生IL-7,局部产生的IL-7可能作为肠黏膜淋巴细胞的一种有效调节因子。