Terminal differentiation of villus tip enterocytes is governed by distinct Tgfβ superfamily members

Author:

Berková Linda1,Fazilaty Hassan2ORCID,Yang Qiutan34567ORCID,Kubovčiak Jan8,Stastna Monika1,Hrckulak Dusan1ORCID,Vojtechova Martina1,Dalessi Tosca2,Brügger Michael David2ORCID,Hausmann George2,Liberali Prisca3ORCID,Korinek Vladimir1ORCID,Basler Konrad2ORCID,Valenta Tomas12ORCID

Affiliation:

1. Laboratory of Cell and Developmental Biology Institute of Molecular Genetics of the Czech Academy of Sciences Prague Czech Republic

2. Department of Molecular Life Sciences University of Zurich Zurich Switzerland

3. Friedrich Miescher Institute for Biomedical Research (FMI) Basel Switzerland

4. State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology Chinese Academy of Sciences Beijing China

5. Institute for Stem Cell and Regeneration, Chinese Academy of Sciences Beijing China

6. Beijing Institute for Stem Cell and Regenerative Medicine Beijing China

7. University of Chinese Academy of Sciences Beijing China

8. Laboratory of Genomics and Bioinformatics Institute of Molecular Genetics of the Czech Academy of Sciences Prague Czech Republic

Abstract

AbstractThe protective and absorptive functions of the intestinal epithelium rely on differentiated enterocytes in the villi. The differentiation of enterocytes is orchestrated by sub‐epithelial mesenchymal cells producing distinct ligands along the villus axis, in particular Bmps and Tgfβ. Here, we show that individual Bmp ligands and Tgfβ drive distinct enterocytic programs specific to villus zonation. Bmp4 is expressed from the centre to the upper part of the villus and activates preferentially genes connected to lipid uptake and metabolism. In contrast, Bmp2 is produced by villus tip mesenchymal cells and it influences the adhesive properties of villus tip epithelial cells and the expression of immunomodulators. Additionally, Tgfβ induces epithelial gene expression programs similar to those triggered by Bmp2. Bmp2‐driven villus tip program is activated by a canonical Bmp receptor type I/Smad‐dependent mechanism. Finally, we establish an organoid cultivation system that enriches villus tip enterocytes and thereby better mimics the cellular composition of the intestinal epithelium. Our data suggest that not only a Bmp gradient but also the activity of individual Bmp drives specific enterocytic programs.

Funder

Grantová Agentura České Republiky

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,Biochemistry

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