2024-03-29T07:21:15Zhttps://eprints.lib.hokudai.ac.jp/dspace-oai/requestoai:eprints.lib.hokudai.ac.jp:2115/601522022-11-17T02:08:08Zhdl_2115_20040hdl_2115_121Visualization of the entire differentiation process of murine M cells : suppression of their maturation in cecal patchesKimura, ShunsukeYamakami-Kimura, MegumiObata, YuukiHase, KojiKitamura, HiroshiOhno, HiroshiIwanaga, Toshihiko490The microfold (M) cell residing in the follicle-associated epithelium is a specialized epithelial cell that initiates mucosal immune responses by sampling lumina! antigens. The differentiation process of M cells remains unclear due to limitations of analytical methods. Here we found that M cells were classified into two functionally different subtypes based on the expression of Glycoprotein 2 (GP2) by newly developed image cytometric analysis. GP2-high M cells actively took up luminal microbeads, whereas GP2-negative or low cells scarcely ingested them, even though both subsets equally expressed the other M-cell signature genes, suggesting that GP2-high M cells represent functionally mature M cells. Further, the GP2-high mature M cells were abundant in Peyer's patch but sparse in the cecal patch: this was most likely due to a decrease in the nuclear translocation of RelB, a downstream transcription factor for the receptor activator of nuclear factor-kappa B signaling. Given that murine cecum contains a protrusion of beneficial commensals, the restriction of M-cell activity might contribute to preventing the onset of any excessive immune response to the commensals through decelerating the M-cell-dependent uptake of microorganisms.Nature Publishing GroupJournal Articleapplication/pdfhttp://hdl.handle.net/2115/60152https://eprints.lib.hokudai.ac.jp/dspace/bitstream/2115/60152/1/manuscript.pdf1933-0219Mucosal immunology836506602015-05enginfo:pmid/25336168info:doi/10.1038/mi.2014.99author