Galibert Laurent, Diemer Geoffrey S, Liu Zhi, Johnson Richard S, Smith Jeffrey L, Walzer Thierry, Comeau Michael R, Rauch Charles T, Wolfson Martin F, Sorensen Rick A, Van der Vuurst de Vries Anne-Renée, Branstetter Daniel G, Koelling Raymond M, Scholler John, Fanslow William C, Baum Peter R, Derry Jonathan M, Yan Wei
Department of Molecular Sciences, Amgen Inc., 1201 Amgen Court, Seattle, WA 98119-3105, USA.
J Biol Chem. 2005 Jun 10;280(23):21955-64. doi: 10.1074/jbc.M502095200. Epub 2005 Mar 21.
Dendritic cells (DCs) are a phenotypically and functionally heterogenous population of leukocytes with distinct subsets serving a different set of specialized immune functions. Here we applied an in vitro whole cell panning approach using antibody phage display technology to identify cell-surface epitopes specifically expressed on human blood BDCA3(+) DCs. A single-chain antibody fragment (anti-1F12 scFv) was isolated that recognizes a conserved surface antigen expressed on both human BDCA3(+) DCs and mouse CD8alpha(+) DCs. We demonstrate that anti-1F12 scFv binds Nectin-like protein 2 (Necl2, Tslc1, SynCaM, SgIGSF, or Igsf4), an adhesion molecule involved in tumor suppression, synapse formation, and spermatogenesis. Thus, Necl2 defines a specialized subset of DCs in both mouse and human. We further show that Necl2 binds Class-I-restricted T-cell-associated molecule (CRTAM), a receptor primarily expressed on activated cytotoxic lymphocytes. When present on antigen presenting cells, Necl2 regulates IL-22 expression by activated CD8(+) T-cells. We propose that Necl2/CRTAM molecular pair could regulate a large panel of cell/cell interactions both within and outside of the immune system.
树突状细胞(DCs)是一类在表型和功能上具有异质性的白细胞群体,其不同亚群发挥着不同的一组特异性免疫功能。在此,我们应用一种使用抗体噬菌体展示技术的体外全细胞淘选方法,来鉴定在人血BDCA3(+) DCs上特异性表达的细胞表面表位。分离出了一种单链抗体片段(抗-1F12 scFv),它识别在人BDCA3(+) DCs和小鼠CD8α(+) DCs上均表达的一种保守表面抗原。我们证明抗-1F12 scFv结合Nectin样蛋白2(Necl2、Tslc1、SynCaM、SgIGSF或Igsf4),这是一种参与肿瘤抑制、突触形成和精子发生的黏附分子。因此,Necl2在小鼠和人类中均定义了DCs的一个特定亚群。我们进一步表明Necl2结合I类限制性T细胞相关分子(CRTAM),这是一种主要在活化的细胞毒性淋巴细胞上表达的受体。当存在于抗原呈递细胞上时,Necl2通过活化的CD8(+) T细胞调节IL-22的表达。我们提出Necl2/CRTAM分子对可能调节免疫系统内外的大量细胞/细胞相互作用。