Distinct populations of crypt-associated fibroblasts act as signaling hubs to control colon homeostasis

0538133 - ÚMG 2021 RIV US eng J - Journal Article
Bruegger, M.D. - Valenta, Tomáš - Fazilaty, H. - Hausmann, G. - Basler, K.
Distinct populations of crypt-associated fibroblasts act as signaling hubs to control colon homeostasis.
PLOS Biology. Roč. 18, č. 12 (2020), č. článku e3001032. ISSN 1544-9173. E-ISSN 1545-7885
R&D Projects: GA ČR(CZ) GA18-21466S
Institutional support: RVO:68378050
Keywords : stem-cells * mesenchymal cells * intestine * myofibroblasts * cytoscape * pathway
OECD category: Biochemistry and molecular biology
Impact factor: 8.029, year: 2020
Method of publishing: Open access
https://journals.plos.org/plosbiology/article?id=10.1371/journal.pbio.3001032

Despite recent progress in recognizing the importance of mesenchymal cells for the homeostasis of the intestinal system, the current picture of how these cells communicate with the associated epithelial layer remains unclear. To describe the relevant cell populations in an unbiased manner, we carried out a single-cell transcriptome analysis of the adult murine colon, producing a high-quality atlas of matched colonic epithelium and mesenchyme. We identify two crypt-associated colonic fibroblast populations that are demarcated by different strengths of platelet-derived growth factor receptor A (Pdgfra) expression. Crypt-bottom fibroblasts (CBFs), close to the intestinal stem cells, express low levels of Pdgfra and secrete canonical Wnt ligands, Wnt potentiators, and bone morphogenetic protein (Bmp) inhibitors. Crypt-top fibroblasts (CTFs) exhibit high Pdgfra levels and secrete noncanonical Wnts and Bmp ligands. While the Pdgfra(low) cells maintain intestinal stem cell proliferation, the Pdgfra(high) cells induce differentiation of the epithelial cells. Our findings enhance our understanding of the crosstalk between various colonic epithelial cells and their associated mesenchymal signaling hubs along the crypt axis-placing differential Pdgfra expression levels in the spotlight of intestinal fibroblast identity.
Permanent Link: http://hdl.handle.net/11104/0315955