Sequential BMP7/TGF-β1 signaling and microbiota instruct mucosal Langerhans cell differentiation.
Tal CapuchaNoam KorenMaria NassarOded HeymanTsipora NirMaayan LevyGili Zilberman-SchapiraKatya ZelentovaLuba Eli-BerchoerMartin ZenkeThomas HieronymusAsaf WilenskyHervé BercovierEran ElinavBjörn E ClausenAvi-Hai HovavPublished in: The Journal of experimental medicine (2018)
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.
Keyphrases
- dendritic cells
- ulcerative colitis
- mesenchymal stem cells
- transforming growth factor
- simultaneous determination
- induced apoptosis
- immune response
- bone regeneration
- cell proliferation
- dna methylation
- genome wide
- peripheral blood
- sensitive detection
- high resolution
- tandem mass spectrometry
- signaling pathway
- gene expression
- tyrosine kinase
- epidermal growth factor receptor
- single molecule