Division of Reproductive and Perinatal Research, Department of Obstetrics, Gynecology and Women's Health, University of Missouri, Columbia, Missouri 65211.
Division of Molecular Biosciences, Faculty of Natural Sciences, Imperial College London, SW7 2AZ, United Kingdom.
Mol Cell Proteomics. 2012 Jan;11(1):M111.008730. doi: 10.1074/mcp.M111.008730. Epub 2011 Oct 10.
DC-SIGN is an immune C-type lectin that is expressed on both immature and mature dendritic cells associated with peripheral and lymphoid tissues in humans. It is a pattern recognition receptor that binds to several pathogens including HIV-1, Ebola virus, Mycobacterium tuberculosis, Candida albicans, Helicobacter pylori, and Schistosoma mansoni. Evidence is now mounting that DC-SIGN also recognizes endogenous glycoproteins, and that such interactions play a major role in maintaining immune homeostasis in humans and mice. Autoantigens (neoantigens) are produced for the first time in the human testes and other organs of the male urogenital tract under androgenic stimulus during puberty. Such antigens trigger autoimmune orchitis if the immune response is not tightly regulated within this system. Endogenous ligands for DC-SIGN could play a role in modulating such responses. Human seminal plasma glycoproteins express a high level of terminal Lewis(x) and Lewis(y) carbohydrate antigens. These epitopes react specifically with the lectin domains of DC-SIGN. However, because the expression of these sequences is necessary but not sufficient for interaction with DC-SIGN, this study was undertaken to determine if any seminal plasma glycoproteins are also endogenous ligands for DC-SIGN. Glycoproteins bearing terminal Lewis(x) and Lewis(y) sequences were initially isolated by lectin affinity chromatography. Protein sequencing established that three tumor biomarker glycoproteins (clusterin, galectin-3 binding glycoprotein, prostatic acid phosphatase) and protein C inhibitor were purified by using this affinity method. The binding of DC-SIGN to these seminal plasma glycoproteins was demonstrated in both Western blot and immunoprecipitation studies. These findings have confirmed that human seminal plasma contains endogenous glycoprotein ligands for DC-SIGN that could play a role in maintaining immune homeostasis both in the male urogenital tract and the vagina after coitus.
DC-SIGN 是一种免疫 C 型凝集素,在人类的外周和淋巴组织中表达于未成熟和成熟的树突状细胞上。它是一种模式识别受体,可与几种病原体结合,包括 HIV-1、埃博拉病毒、结核分枝杆菌、白色念珠菌、幽门螺杆菌和曼氏血吸虫。现在有越来越多的证据表明,DC-SIGN 还识别内源性糖蛋白,并且这些相互作用在维持人类和小鼠的免疫稳态中起着重要作用。自身抗原(新抗原)在青春期雄激素刺激下首次在人睾丸和男性泌尿生殖道的其他器官中产生。如果免疫反应在该系统内不能被紧密调节,这些抗原会引发自身免疫性睾丸炎。DC-SIGN 的内源性配体可能在调节这种反应中发挥作用。人精液糖蛋白表达高水平的末端 Lewis(x)和 Lewis(y)碳水化合物抗原。这些表位与 DC-SIGN 的凝集素结构域特异性反应。然而,由于这些序列的表达对于与 DC-SIGN 的相互作用是必要的但不是充分的,因此进行了这项研究以确定任何精液糖蛋白是否也是 DC-SIGN 的内源性配体。带有末端 Lewis(x)和 Lewis(y)序列的糖蛋白最初通过凝集素亲和层析分离。蛋白质测序确定了三种肿瘤生物标志物糖蛋白(聚集素、半乳糖凝集素-3 结合糖蛋白、前列腺酸性磷酸酶)和蛋白 C 抑制剂是通过这种亲和方法纯化的。在 Western blot 和免疫沉淀研究中均证实了 DC-SIGN 与这些精液糖蛋白的结合。这些发现证实了人类精液中含有 DC-SIGN 的内源性糖蛋白配体,这些配体可能在性交后男性泌尿生殖道和阴道中维持免疫稳态中发挥作用。