TY - JOUR
T1 - Human gut M cells resemble dendritic cells and present gluten antigen
AU - Wang, Daisong
AU - Lim, Sangho
AU - van de Wetering, Willine J
AU - Lopez-Iglesias, Carmen
AU - Okura, Yuu
AU - Teranishi-Ikawa, Yuri
AU - Mizoroki, Akihiko
AU - Spoelstra, Willem Kasper
AU - Dayton, Talya
AU - van Son, Gijs J F
AU - Pronk, Apollo
AU - Smakman, Niels
AU - Gonera-de Jong, Gieneke B C
AU - Withoff, Sebo
AU - Jonkers, Iris H
AU - van Zon, Jeroen S
AU - Tans, Sander J
AU - Peters, Peter J
AU - van Es, Johan H
AU - Clevers, Hans
N1 - © 2025. The Author(s).
PY - 2025/12/10
Y1 - 2025/12/10
N2 - Microfold (M) cells are rare intestinal epithelial cells that reside in the follicle-associated epithelium of Peyer's patches
1. M cells transport luminal antigens to submucosal antigen-presenting cells
2,3. These insights primarily derive from transmission electron microscopy and studies using genetically modified mice
2-4. Here we establish an intestinal organoid model to study human M cells and reconstruct the differentiation trajectory of M cells through transcriptome profiling. The results indicate that as well as facilitating luminal antigen transport, human M cells also directly present antigens via the class II major histocompatibility complex (MHC-II). Notably, the related enterocytes only express MHC-II in chronic inflammatory states and do not express typical dendritic cell markers. Human M cells physiologically express a gene profile that resembles that of dendritic cells. Similar to dendritic cells, M cell development is induced by RANKL and CSF2 and requires the transcription factors SPIB and RUNX2. HLA-DQ2.5 M cells process and present gluten antigen as demonstrated in organoid-T cell co-culture assays. These findings suggest that M cells may have a central role in coeliac disease.
AB - Microfold (M) cells are rare intestinal epithelial cells that reside in the follicle-associated epithelium of Peyer's patches
1. M cells transport luminal antigens to submucosal antigen-presenting cells
2,3. These insights primarily derive from transmission electron microscopy and studies using genetically modified mice
2-4. Here we establish an intestinal organoid model to study human M cells and reconstruct the differentiation trajectory of M cells through transcriptome profiling. The results indicate that as well as facilitating luminal antigen transport, human M cells also directly present antigens via the class II major histocompatibility complex (MHC-II). Notably, the related enterocytes only express MHC-II in chronic inflammatory states and do not express typical dendritic cell markers. Human M cells physiologically express a gene profile that resembles that of dendritic cells. Similar to dendritic cells, M cell development is induced by RANKL and CSF2 and requires the transcription factors SPIB and RUNX2. HLA-DQ2.5 M cells process and present gluten antigen as demonstrated in organoid-T cell co-culture assays. These findings suggest that M cells may have a central role in coeliac disease.
U2 - 10.1038/s41586-025-09829-8
DO - 10.1038/s41586-025-09829-8
M3 - Article
C2 - 41372409
SN - 0028-0836
JO - Nature
JF - Nature
ER -