Center for Molecular Immunology and Infectious Diseases and Department of Veterinary and Biomedical Sciences, The Pennsylvania State University, University Park, PA 16802, USA.
Protein Cell. 2012 Aug;3(8):571-80. doi: 10.1007/s13238-012-2927-3. Epub 2012 Jun 8.
Epithelial tissues covering the external and internal surface of a body are constantly under physical, chemical or biological assaults. To protect the epithelial tissues and maintain their homeostasis, multiple layers of immune defense mechanisms are required. Besides the epithelial tissue-resident immune cells that provide the first line of defense, circulating immune cells are also recruited into the local tissues in response to challenges. Chemokines and chemokine receptors regulate tissue-specific migration, maintenance and functions of immune cells. Among them, chemokine receptor CCR10 and its ligands chemokines CCL27 and CCL28 are uniquely involved in the epithelial immunity. CCL27 is expressed predominantly in the skin by keratinocytes while CCL28 is expressed by epithelial cells of various mucosal tissues. CCR10 is expressed by various subsets of innate-like T cells that are programmed to localize to the skin during their developmental processes in the thymus. Circulating T cells might be imprinted by skin-associated antigen- presenting cells to express CCR10 for their recruitment to the skin during the local immune response. On the other hand, IgA antibody-producing B cells generated in mucosa-associated lymphoid tissues express CCR10 for their migration and maintenance at mucosal sites. Increasing evidence also found that CCR10/ligands are involved in regulation of other immune cells in epithelial immunity and are frequently exploited by epithelium-localizing or -originated cancer cells for their survival, proliferation and evasion from immune surveillance. Herein, we review current knowledge on roles of CCR10/ligands in regulation of epithelial immunity and diseases and speculate on related important questions worth further investigation.
覆盖身体内外表面的上皮组织不断受到物理、化学或生物的攻击。为了保护上皮组织并维持其体内平衡,需要多层次的免疫防御机制。除了提供第一道防线的上皮组织固有免疫细胞外,循环免疫细胞也会在受到挑战时被招募到局部组织中。趋化因子和趋化因子受体调节免疫细胞的组织特异性迁移、维持和功能。其中,趋化因子受体 CCR10 及其配体趋化因子 CCL27 和 CCL28 独特地参与上皮免疫。CCL27 主要由角质形成细胞在皮肤中表达,而 CCL28 则由各种黏膜组织的上皮细胞表达。CCR10 由各种先天样 T 细胞亚群表达,这些细胞在胸腺发育过程中被编程定位于皮肤。循环 T 细胞可能被皮肤相关抗原呈递细胞印记以表达 CCR10,以便在局部免疫反应期间募集到皮肤。另一方面,黏膜相关淋巴组织中产生的 IgA 抗体产生 B 细胞为其在黏膜部位的迁移和维持表达 CCR10。越来越多的证据还发现,CCR10/配体参与调节上皮免疫中的其他免疫细胞,并且经常被定位于上皮或起源于上皮的癌细胞利用来生存、增殖和逃避免疫监视。在此,我们综述了 CCR10/配体在调节上皮免疫和疾病中的作用的最新知识,并推测了一些值得进一步研究的相关重要问题。