| Literature DB >> 31775048 |
Kazufumi Kunimura1, Daiji Sakata2, Xin Tun3, Takehito Uruno2, Miho Ushijima1, Tomoya Katakai4, Akira Shiraishi5, Ryosuke Aihara1, Yasuhisa Kamikaseda1, Keisuke Matsubara1, Hirokazu Kanegane6, Shinichiro Sawa7, Gérard Eberl8, Shouichi Ohga5, Yasunobu Yoshikai3, Yoshinori Fukui9.
Abstract
Intestinal microfold cells (M cells) in Peyer's patches are a special subset of epithelial cells that initiate mucosal immune responses through uptake of luminal antigens. Although the cytokine receptor activator of nuclear factor-κB ligand (RANKL) expressed on mesenchymal cells triggers differentiation into M cells, other environmental cues remain unknown. Here, we show that the metastasis-promoting protein S100A4 is required for development of mature M cells. S100A4-producing cells are a heterogenous cell population including lysozyme-expressing dendritic cells and group 3 innate lymphoid cells. We found that in the absence of DOCK8, a Cdc42 activator critical for interstitial leukocyte migration, S100A4-producing cells are reduced in the subepithelial dome, resulting in a maturation defect of M cells. While S100A4 promotes differentiation into mature M cells in organoid culture, genetic inactivation of S100a4 prevents the development of mature M cells in mice. Thus, S100A4 is a key environmental cue that regulates M cell differentiation in collaboration with RANKL.Entities:
Keywords: DOCK8; M cell maturation; Peyer's patch; S100A4-producing cells; intestinal immunity
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Year: 2019 PMID: 31775048 DOI: 10.1016/j.celrep.2019.10.091
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423