TY - JOUR
T1 - Development of intestinal M cells and follicle-associated epithelium is regulated by TRAF6-mediated NF-κB signaling
AU - Kanaya, Takashi
AU - Sakakibara, Sayuri
AU - Jinnohara, Toshi
AU - Hachisuka, Masami
AU - Tachibana, Naoko
AU - Hidano, Shinya
AU - Kobayashi, Takashi
AU - Kimura, Shunsuke
AU - Iwanaga, Toshihiko
AU - Nakagawa, Tomoo
AU - Katsuno, Tatsuro
AU - Kato, Naoya
AU - Akiyama, Taishin
AU - Sato, Toshiro
AU - Williams, Ifor R.
AU - Ohno, Hiroshi
N1 - Funding Information:
This work was supported in part by the Japan Society for the Promotion of Science KAKENHI (grant 26460584 to T. Kanaya and grant 24249029 to H. Ohno), Ministry of Education, Culture, Sports, Science and Technology KAKENHI (grant 15H01165 to T. Kanaya and grant 20113003 to H. Ohno), Uehara Memorial Foundation (grant to T. Kanaya), Takeda Science Foundation (grant to T. Kanaya), and Mo-chida Memorial Foundation for Medical and Pharmaceutical Research (grant to T.K.). The authors declare no competing financial interests.
Publisher Copyright:
© 2018 Kanaya et al.
PY - 2018/2/1
Y1 - 2018/2/1
N2 - M cells are located in the follicle-associated epithelium (FAE) that covers Peyer's patches (PPs) and are responsible for the uptake of intestinal antigens. The differentiation of M cells is initiated by receptor activator of NF-κB. However, the intracellular pathways involved in M cell differentiation are still elusive. In this study, we demonstrate that the NF-κB pathway activated by RANK is essential for M cell differentiation using in vitro organoid culture. Overexpression of NF-κB transcription factors enhances the expression of M cell-associated molecules but is not sufficient to complete M cell differentiation. Furthermore, we evaluated the requirement for tumor necrosis factor receptor-associated factor 6 (TRAF6). Conditional deletion of TRAF6 in the intestinal epithelium causes a complete loss of M cells in PPs, resulting in impaired antigen uptake into PPs. In addition, the expression of FAE-associated genes is almost silenced in TRAF6-deficient mice. This study thus demonstrates the crucial role of TRAF6-mediated NF-κB signaling in the development of M cells and FAE.
AB - M cells are located in the follicle-associated epithelium (FAE) that covers Peyer's patches (PPs) and are responsible for the uptake of intestinal antigens. The differentiation of M cells is initiated by receptor activator of NF-κB. However, the intracellular pathways involved in M cell differentiation are still elusive. In this study, we demonstrate that the NF-κB pathway activated by RANK is essential for M cell differentiation using in vitro organoid culture. Overexpression of NF-κB transcription factors enhances the expression of M cell-associated molecules but is not sufficient to complete M cell differentiation. Furthermore, we evaluated the requirement for tumor necrosis factor receptor-associated factor 6 (TRAF6). Conditional deletion of TRAF6 in the intestinal epithelium causes a complete loss of M cells in PPs, resulting in impaired antigen uptake into PPs. In addition, the expression of FAE-associated genes is almost silenced in TRAF6-deficient mice. This study thus demonstrates the crucial role of TRAF6-mediated NF-κB signaling in the development of M cells and FAE.
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U2 - 10.1084/jem.20160659
DO - 10.1084/jem.20160659
M3 - Article
C2 - 29339448
AN - SCOPUS:85041426883
SN - 0022-1007
VL - 215
SP - 501
EP - 519
JO - Journal of Experimental Medicine
JF - Journal of Experimental Medicine
IS - 2
ER -