| Literature DB >> 31080135 |
Lara Planas-Paz1, Tianliang Sun1, Monika Pikiolek1, Nadire R Cochran2, Sebastian Bergling1, Vanessa Orsini1, Zinger Yang2, Frederic Sigoillot2, Jasna Jetzer1, Maryam Syed1, Marilisa Neri1, Sven Schuierer1, Lapo Morelli1, Philipp S Hoppe1, Wibke Schwarzer1, Carlos M Cobos3, John L Alford2, Le Zhang2, Rachel Cuttat1, Annick Waldt1, Nicole Carballido-Perrig1, Florian Nigsch1, Bernd Kinzel1, Thomas B Nicholson2, Yi Yang2, Xiaohong Mao2, Luigi M Terracciano4, Carsten Russ2, John S Reece-Hoyes2, Caroline Gubser Keller1, Andreas W Sailer1, Tewis Bouwmeester1, Linda E Greenbaum5, Jesse J Lugus2, Feng Cong2, Gregory McAllister2, Gregory R Hoffman2, Guglielmo Roma1, Jan S Tchorz6.
Abstract
Biliary epithelial cells (BECs) form bile ducts in the liver and are facultative liver stem cells that establish a ductular reaction (DR) to support liver regeneration following injury. Liver damage induces periportal LGR5+ putative liver stem cells that can form BEC-like organoids, suggesting that RSPO-LGR4/5-mediated WNT/β-catenin activity is important for a DR. We addressed the roles of this and other signaling pathways in a DR by performing a focused CRISPR-based loss-of-function screen in BEC-like organoids, followed by in vivo validation and single-cell RNA sequencing. We found that BECs lack and do not require LGR4/5-mediated WNT/β-catenin signaling during a DR, whereas YAP and mTORC1 signaling are required for this process. Upregulation of AXIN2 and LGR5 is required in hepatocytes to enable their regenerative capacity in response to injury. Together, these data highlight heterogeneity within the BEC pool, delineate signaling pathways involved in a DR, and clarify the identity and roles of injury-induced periportal LGR5+ cells.Entities:
Keywords: CRISPR screen; LGR5; YAP; ductular reaction; hepatic progenitor cell; liver organoids; liver stem cells; oval cell; regeneration; single-cell RNA sequencing
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Year: 2019 PMID: 31080135 DOI: 10.1016/j.stem.2019.04.005
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633