Anisotropic expansion of hepatocyte lumina enforced by apical bulkheads

Author:

Belicova Lenka1ORCID,Repnik Urska1,Delpierre Julien1ORCID,Gralinska Elzbieta2ORCID,Seifert Sarah1,Valenzuela José Ignacio1,Morales-Navarrete Hernán Andrés1ORCID,Franke Christian1ORCID,Räägel Helin13,Shcherbinina Evgeniya4,Prikazchikova Tatiana4,Koteliansky Victor4,Vingron Martin2,Kalaidzidis Yannis L.1ORCID,Zatsepin Timofei45ORCID,Zerial Marino1ORCID

Affiliation:

1. Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany

2. Department of Computational Molecular Biology, Max Planck Institute for Molecular Genetics, Berlin, Germany

3. Nelson Laboratories LLC, Salt Lake City, UT

4. Skolkovo Institute of Science and Technology, Skolkovo, Russia

5. Department of Chemistry, Lomonosov Moscow State University, Moscow, Russia

Abstract

Lumen morphogenesis results from the interplay between molecular pathways and mechanical forces. In several organs, epithelial cells share their apical surfaces to form a tubular lumen. In the liver, however, hepatocytes share the apical surface only between adjacent cells and form narrow lumina that grow anisotropically, generating a 3D network of bile canaliculi (BC). Here, by studying lumenogenesis in differentiating mouse hepatoblasts in vitro, we discovered that adjacent hepatocytes assemble a pattern of specific extensions of the apical membrane traversing the lumen and ensuring its anisotropic expansion. These previously unrecognized structures form a pattern, reminiscent of the bulkheads of boats, also present in the developing and adult liver. Silencing of Rab35 resulted in loss of apical bulkheads and lumen anisotropy, leading to cyst formation. Strikingly, we could reengineer hepatocyte polarity in embryonic liver tissue, converting BC into epithelial tubes. Our results suggest that apical bulkheads are cell-intrinsic anisotropic mechanical elements that determine the elongation of BC during liver tissue morphogenesis.

Funder

German Federal Ministry of Research and Education

European Research Council

Deutsche Forschungsgemeinschaft

Technische Universität Dresden

Max Planck Society

Publisher

Rockefeller University Press

Subject

Cell Biology

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