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PAR-4/LKB1 prevents intestinal hyperplasia by restricting endoderm specification in C. elegans embryos
Flora Demouchy, Ophélie Nicolle, Grégoire Michaux, Anne Pacquelet

PAR-4/LKB1 prevents intestinal hyperplasia by restricting endoderm specification in C. elegans embryos

Science & Mathematics Published 2024 Verification Pending

Overview & Synopsis

The kinase PAR-4/LKB1 is a major regulator of intestinal homeostasis, which prevents polyposis in humans. Moreover, its ectopic activation is sufficient to induce polarization and formation of microvilli-like structures in intestinal cell lines. Here, we use Caenorhabditis elegans to examine the role of PAR-4 during intestinal development in vivo. We show that it is not required to establish enterocyte polarity and plays only a minor role in brush border formation. By contrast, par-4 mutants display severe deformations of the intestinal lumen as well as supernumerary intestinal cells, thereby revealing a previously unappreciated function of PAR-4 in preventing intestinal hyperplasia. The presence of supernumerary enterocytes in par-4 mutants is not due to excessive cell proliferation, but rather to the abnormal expression of the intestinal cell fate factors end-1 and elt-2 outside the E lineage. Notably, par-4 mutants also display reduced expression of end-1 and elt-2 inside the E lineage. Our work thereby unveils an essential and dual role of PAR-4, which both restricts intestinal specification to the E lineage and ensures its robust differentiation.

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Document Information

Document Title PAR-4/LKB1 prevents intestinal hyperplasia by restricting endoderm specification in C. elegans embryos
Author / Organization Flora Demouchy, Ophélie Nicolle, Grégoire Michaux, Anne Pacquelet
Subject & Discipline Multidisciplinary Academic Open Research
Categories Science & Mathematics
Publication Year 2024
License / Rights Open Access / Creative Commons
Resource Verification Listed PDF (Verification Pending)
Original Host Website HAL Open Science (hal.science)
File Format application/pdf (Portable Document Format)
Language EN
Catalog ID DOC-181862
Original Source Link Visit Source Page on hal.science »