Cited by 133Liver physiology and pathologyMetabolism, Diabetes, and CancerDrug-Induced Hepatotoxicity and Protection

Metabolic Remodeling during Liver Regeneration

Open access
Caldez, Matias J., Van Hul, Noémi, Koh, Hiromi W.L., Teo, Xing Qi, Fan, Jun Jun, Tan, Peck Yean, Dewhurst, Matthew R., Too, Peh Gek +9 more·2018·Developmental Cell

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.

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Crossref · 10.1016/j.devcel.2018.09.020

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  • Following two-thirds PHx, the abrupt loss of liver mass is overcome by coordinated hepatocyte proliferation and metabolic adaptation through a division of labor among remaining hepatocytes.

    “Following two-thirds partial hepatectomy (PHx), a well-established model of liver regeneration, the abrupt loss of liver mass is overcome by coordinated hepatocyte proliferation and metabolic adaptation through a division of labor among the remaining hepatocytes.2”

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References 64 · Cited by 133

Authors
Caldez, M. J., Van Hul, N., Koh, H. W. L., Teo, X. Q., Fan, J. J., Tan, P. Y., Dewhurst, M. R., Too, P. G., Talib, S. Z. A., Chiang, B. E., Stünkel, W., Yu, H., Lee, P., Fuhrer, T., Choi, H., Björklund, M., & Kaldis, P.
Affiliations
  • Agency for Science, Technology and Research (SG)
  • National University of Singapore (SG)
  • Singapore Bioimaging Consortium (SG)
  • ETH Zurich (CH)
  • Zhejiang University-University of Edinburgh Institute (CN)
Corresponding author
Kaldis, Philipp
Venue
Developmental Cell
Publisher
Elsevier BV
Published
2018-11
Volume
47
Issue
4
Pages
425-438.e5
ISSN
1534-5807 (ISSN-L)
OpenAlex
W2897916903
Cited by
133
References
64
Citations by year
2026: 17 · 2025: 18 · 2024: 16 · 2023: 29 · 2022: 15 · 2021: 15 · 2020: 16 · 2019: 7
FWCI
5.95
Type
journal article
Language
en
Open access
Locations
  • Developmental Cell (publishedVersion)
  • PubMed (publishedVersion)
  • Lund University Publications (Lund University) (submittedVersion)
Funders
  • Biomedical Research Council (1231AFG031)
  • Agency for Science, Technology and Research
  • SINGA
  • Institute of Bioengineering and Nanotechnology (1334i00051)
  • NMRC (R-185-000-294-511)
  • SMART BioSyM and Mechanobiology Institute of Singapore (R-714-001-003-271)
Topics
  • Health Sciences › Medicine › Hepatology › Liver physiology and pathology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Drug-Induced Hepatotoxicity and Protection
Keywords
liver regeneration, metabolic remodeling, mitochondrial dysfunction, oxidative phosphorylation, redox ratio, alanine aminotransferase, alanine production, alpha-ketoglutarate, pyruvate metabolism, hepatocyte metabolism, transcriptomics, metabolomics, redox imaging
MeSH terms
Animals, Liver, Liver Regeneration, Mitochondria, Pyruvic Acid, Hepatocytes, Metabolomics

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