Author:
Huycke Tyler R.,Miyazaki Hikaru,Häkkinen Teemu J.,Srivastava Vasudha,Barruet Emilie,McGinnis Christopher S.,Kalantari Ali,Cornwall-Scoones Jake,Vaka Dedeepya,Zhu Qin,Jo Hyunil,DeGrado William F.,Thomson Matt,Garikipati Krishna,Boffelli Dario,Klein Ophir D.,Gartner Zev J.
Abstract
ABSTRACTTissue folding generates structural motifs critical to organ function. In the intestine, bending of a flat epithelium into a periodic pattern of folds gives rise to villi, the numerous finger-like protrusions that are essential for nutrient absorption. However, the molecular and mechanical mechanisms driving the initiation and morphogenesis of villi remain a matter of debate. Here, we identify an active mechanical mechanism that simultaneously patterns and folds intestinal villi. We find that PDGFRA+ subepithelial mesenchymal cells generate myosin II-dependent forces sufficient to produce patterned curvature in neighboring tissue interfaces. At the cell-level, this occurs through a process dependent upon matrix metalloproteinase-mediated tissue fluidization and altered cell-ECM adhesion. By combining computational models within vivoexperiments, we reveal these cellular features manifest at the tissue-level as differences in interfacial tensions that promote mesenchymal aggregation and interface bending through a process analogous to the active de-wetting of a thin liquid film.
Publisher
Cold Spring Harbor Laboratory
Cited by
2 articles.
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