Polycomb Repressive Complex 2-controlled Essrg regulates intestinal Microfold cell differentiation.
Joel Johnson George, Mikko Oittinen, Laura Martín-DíaziD, Veronika ZapilkoiD, Sharif IqbaliD, Terhi RintakangasiD, Fábio Tadeu Arrojo MartinsiD, Henri NiskaneniD, Pekka KatajistoiD, Minna Unelma KaikkoneniD, Keijo M. ViiriiD
Abstract
Microfold cells (M cells) are immunosurveillance epithelial cells located in the Peyers patches in the intestine responsible for monitoring and transcytosis of antigens, microorganisms and pathogens. Many transcription factors, e.g., Spi-B and Sox8, necessary to M cell differentiation have been described but the exhaustive set of factors sufficient for differentiation and development of a mature M cell remains elusive. Moreover, the role of polycomb repressive complex 2 (PRC2) as an epigenetic regulator of M cell development has not yet been interrogated. Here, we show that PRC2 regulates a significant set of genes during the M cell differentiation including many transcription factors. Estrogen related receptor gamma (Esrrg) is a novel M cell specific transcription factor acting on a RankL-Rank induced NF-kB pathway, upstream of Sox8 and necessary but not sufficient for a mature M cell marker Gp2 expression. To conclude, with the aid of PRC2 target survey we identified the list of developmental genes specifically implicated in M cell development and Essrg as a necessary factor for Sox8-mediated M cell differentiation.
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