| Literature DB >> 30344111 |
Matias J Caldez1, Noémi Van Hul2, Hiromi W L Koh3, Xing Qi Teo4, Jun Jun Fan5, Peck Yean Tan6, Matthew R Dewhurst7, Peh Gek Too6, S Zakiah A Talib2, Beatrice E Chiang2, Walter Stünkel6, Hanry Yu8, Philip Lee4, Tobias Fuhrer9, Hyungwon Choi10, Mikael Björklund11, Philipp Kaldis12.
Abstract
Liver disease is linked to a decreased capacity of hepatocytes to divide. In addition, cellular metabolism is important for tissue homeostasis and regeneration. Since metabolic changes are a hallmark of liver disease, we investigated the connections between metabolism and cell division. We determined global metabolic changes at different stages of liver regeneration using a combination of integrated transcriptomic and metabolomic analyses with advanced functional redox in vivo imaging. Our data indicate that blocking hepatocyte division during regeneration leads to mitochondrial dysfunction and downregulation of oxidative pathways. This resulted in an increased redox ratio and hyperactivity of alanine transaminase allowing the production of alanine and α-ketoglutarate from pyruvate when mitochondrial functions are impaired. Our data suggests that during liver regeneration, cell division leads to hepatic metabolic remodeling. Moreover, we demonstrate that hepatocytes are equipped with a flexible metabolic machinery able to adapt dynamically to changes during tissue regeneration.Entities:
Keywords: Cdk1; advanced molecular imaging; alanine transaminase; amino acids; glucose; liver regeneration; metabolic flux; metabolomics; mitochondrial oxidation; transcriptomics
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Year: 2018 PMID: 30344111 DOI: 10.1016/j.devcel.2018.09.020
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270