Division of Biomedical Sciences, University of California School of Medicine, Riverside, CA 92521, USA.
Trends Immunol. 2018 Mar;39(3):185-195. doi: 10.1016/j.it.2017.09.002. Epub 2017 Sep 22.
Microfold (M) cells are epithelial cells present in mucosal tissues and specialized for the capture of luminal microparticles and their delivery to underlying immune cells; thus, they are crucial participants in mucosal immune surveillance. Multiple phenotypic subsets of M cells have now been described, all sharing a unique apical morphology that provides clues to their ability to capture microbial particles. The existence of diverse M cell phenotypes, especially inflammation-inducible M cells, provides an intriguing puzzle: some variants may augment luminal surveillance to boost mucosal immunity, while others may promote microbial access to tissues. Here, I consider the unique induction requirements of each M cell subset and functional differences, highlighting the potentially distinct consequences in mucosal immunity.
微皱褶(M)细胞是存在于黏膜组织中的上皮细胞,专门用于捕获腔内分泌的微粒,并将其递送至下方的免疫细胞;因此,它们是黏膜免疫监视的关键参与者。现在已经描述了多种表型亚群的 M 细胞,它们都具有独特的顶端形态,这为它们捕获微生物颗粒的能力提供了线索。不同的 M 细胞表型的存在,特别是炎症诱导的 M 细胞,提供了一个有趣的难题:一些变体可能会增强腔内分泌的监视,以增强黏膜免疫,而另一些变体则可能促进微生物进入组织。在这里,我考虑了每个 M 细胞亚群的独特诱导要求和功能差异,强调了在黏膜免疫中可能存在的不同后果。