Lgr5+ telocytes are a signaling source at the intestinal villus tip

Keren Bahar Halpern(Weizmann Institute of Science), Hassan Massalha(Weizmann Institute of Science), Rachel K. Zwick(University of California, San Francisco), Andreas E. Moor(University of Zurich), David Castillo‐Azofeifa(University of California, San Francisco), Milena Rozenberg(Weizmann Institute of Science), Lydia Farack(Weizmann Institute of Science), Adi Egozi(Weizmann Institute of Science), Dan R. Miller(Weizmann Institute of Science), Inna Averbukh(Weizmann Institute of Science), Yotam Harnik(Weizmann Institute of Science), Noa Weinberg-Corem, Frédéric J. de Sauvage(Molecular Oncology (United States)), Ido Amit(Weizmann Institute of Science), Ophir D. Klein(University of California, San Francisco), Michal Shoshkes-Carmel(Hebrew University of Jerusalem), Shalev Itzkovitz(Weizmann Institute of Science)
Nature Communications
April 22, 2020
Cited by 160Open Access
Full Text

Abstract

The intestinal epithelium is a structured organ composed of crypts harboring Lgr5+ stem cells, and villi harboring differentiated cells. Spatial transcriptomics have demonstrated profound zonation of epithelial gene expression along the villus axis, but the mechanisms shaping this spatial variability are unknown. Here, we combine laser capture micro-dissection and single cell RNA sequencing to uncover spatially zonated populations of mesenchymal cells along the crypt-villus axis. These include villus tip telocytes (VTTs) that express Lgr5, a gene previously considered a specific crypt epithelial stem cell marker. VTTs are elongated cells that line the villus tip epithelium and signal through Bmp morphogens and the non-canonical Wnt5a ligand. Their ablation is associated with perturbed zonation of enterocyte genes induced at the villus tip. Our study provides a spatially-resolved cell atlas of the small intestinal stroma and exposes Lgr5+ villus tip telocytes as regulators of the epithelial spatial expression programs along the villus axis.


Related Papers

No related papers found

Powered by citation graph analysis