Sequential BMP7/TGF-β1 signaling and microbiota instruct mucosal Langerhans cell differentiation

Author:

Capucha Tal1ORCID,Koren Noam1ORCID,Nassar Maria1,Heyman Oded2,Nir Tsipora1,Levy Maayan3,Zilberman-Schapira Gili3,Zelentova Katya1,Eli-Berchoer Luba1,Zenke Martin4,Hieronymus Thomas4,Wilensky Asaf2,Bercovier Herve5ORCID,Elinav Eran3,Clausen Björn E.6ORCID,Hovav Avi-Hai1ORCID

Affiliation:

1. The Institute of Dental Sciences, Hebrew University–Hadassah Medical Center, Jerusalem, Israel

2. Department of Periodontology, Faculty of Dental Medicine, Hebrew University–Hadassah Medical Center, Jerusalem, Israel

3. Department of Immunology, Weizmann Institute of Science, Rehovot, Israel

4. Institute for Biomedical Engineering, Department of Cell Biology, Medical Faculty and Helmholtz Institute for Biomedical Engineering, RWTH Aachen University, Aachen, Germany

5. Department of Microbiology and Molecular Genetics, Faculty of Medicine, Hebrew University, Jerusalem, Israel

6. Institute for Molecular Medicine, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany

Abstract

Mucosal Langerhans cells (LCs) originate from pre–dendritic cells and monocytes. However, the mechanisms involved in their in situ development remain unclear. Here, we demonstrate that the differentiation of murine mucosal LCs is a two-step process. In the lamina propria, signaling via BMP7-ALK3 promotes translocation of LC precursors to the epithelium. Within the epithelium, TGF-β1 finalizes LC differentiation, and ALK5 is crucial to this process. Moreover, the local microbiota has a major impact on the development of mucosal LCs, whereas LCs in turn maintain mucosal homeostasis and prevent tissue destruction. These results reveal the differential and sequential role of TGF-β1 and BMP7 in LC differentiation and highlight the intimate interplay of LCs with the microbiota.

Funder

Israel Science Foundation

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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