| Literature DB >> 29466728 |
Vanessa Maillet1, Nadia Boussetta1, Jocelyne Leclerc1, Véronique Fauveau1, Marc Foretz1, Benoit Viollet1, Jean-Pierre Couty2, Séverine Celton-Morizur1, Christine Perret1, Chantal Desdouets3.
Abstract
Liver kinase B1 (LKB1) is involved in several biological processes and is a key regulator of hepatic metabolism and polarity. Here, we demonstrate that the master kinase LKB1 plays a dual role in liver regeneration, independently of its major target, AMP-activated protein kinase (AMPK). We found that the loss of hepatic Lkb1 expression promoted hepatocyte proliferation acceleration independently of metabolic/energetic balance. LKB1 regulates G0/G1 progression, specifically by controlling epidermal growth factor receptor (EGFR) signaling. Furthermore, later in regeneration, LKB1 controls mitotic fidelity. The deletion of Lkb1 results in major alterations to mitotic spindle formation along the polarity axis. Thus, LKB1 deficiency alters ploidy profile at late stages of regeneration. Our findings highlight the dual role of LKB1 in liver regeneration, as a guardian of hepatocyte proliferation and genomic integrity.Entities:
Keywords: EGFR; LKB1; hepatocytes; liver regeneration; microtubule spindle; mitosis fidelity; polyploidy
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Year: 2018 PMID: 29466728 DOI: 10.1016/j.celrep.2018.01.086
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423