Evidence map›Paper›PMID 26126685›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2015

Characterization of lipid metabolism in a novel immortalized human hepatocyte cell line.

Charlotte J Green, Deborah Johnson, Harsh D Amin, Pamela Sivathondan, Michael A Silva, Lai Mun Wang, Lara Stevanato, Catriona A McNeil, Erik A Miljan, John D Sinden and 2 more

Open access · hybridAbstract read
In one paragraph

Article in American journal of physiology. Endocrinology and metabolism, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.5field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Immortalization Reversibility in the Context of Cell Therapy Biosafety.International journal of molecular sciences · 2023
    Review
  7. Article
  8. Customized liver organoids as an advancedInternational journal of biological sciences · 2023
    Review
  9. Article
  10. iScience · 2022
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 1 country.

Charlotte J GreenOxford Centre for Diabetes, Endocrinology and Metabolism, University of Oxford, Churchill Hospital, Oxford, United Kingdom;
Deborah JohnsonReNeuron Group, Guildford, Surrey, United Kingdom;
Harsh D AminReNeuron Group, Guildford, Surrey, United Kingdom;
Pamela SivathondanNuffield Department of Obstetrics and Gynaecology, The Women's Centre, University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom;
Michael A SilvaDepartment of Hepatobiliary and Pancreatic Surgery, Oxford University Hospital NHS Trust, Churchill Hospital, Oxford, United Kingdom; and.
Lai Mun WangDepartment of Cellular Pathology, Oxford University Hospitals, Oxford, United Kingdom.
Lara StevanatoReNeuron Group, Guildford, Surrey, United Kingdom;
Catriona A McNeilOxford Centre for Diabetes, Endocrinology and Metabolism, University of Oxford, Churchill Hospital, Oxford, United Kingdom;
Erik A MiljanReNeuron Group, Guildford, Surrey, United Kingdom;
John D SindenReNeuron Group, Guildford, Surrey, United Kingdom;
Karl J MortenNuffield Department of Obstetrics and Gynaecology, The Women's Centre, University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom;
Leanne HodsonOxford Centre for Diabetes, Endocrinology and Metabolism, University of Oxford, Churchill Hospital, Oxford, United Kingdom; leanne.hodson@ocdem.ox.ac.uk.ORCID http://orcid.org/0000-0002-2648-6526
ReNeuron (United Kingdom) · GBChurchill Hospital · GBJohn Radcliffe Hospital · GBOxford University Hospitals NHS Trust · GB

Funding

British Heart Foundation FS/11/18/28633
6 · The paper itself

Abstract

The development of hepatocyte cell models that represent fatty acid partitioning within the human liver would be beneficial for the study of the development and progression of nonalcoholic fatty liver disease (NAFLD). We sought to develop and characterize a novel human liver cell line (LIV0APOLY) to establish a model of lipid accumulation using a physiological mixture of fatty acids under low- and high-glucose conditions. LIV0APOLY cells were compared with a well-established cell line (HepG2) and, where possible, primary human hepatocytes. LIV0APOLY cells were found to proliferate and express some mature liver markers and were wild type for the PNPLA3 (rs738409) gene, whereas HepG2 cells carried the Ile(148)Met variant that is positively associated with liver fat content. Intracellular triglyceride content was higher in HepG2 than in LIV0APOLY cells; exposure to high glucose and/or exogenous fatty acids increased intracellular triglyceride in both cell lines. Triglyceride concentrations in media were higher from LIV0APOLY compared with HepG2 cells. Culturing LIV0APOLY cells in high glucose increased a marker of endoplasmic reticulum stress and attenuated insulin-stimulated Akt phosphorylation whereas low glucose and exogenous fatty acids increased AMPK phosphorylation. Although LIV0APOLY cells and primary hepatocytes stored similar amounts of exogenous fatty acids as triglyceride, more exogenous fatty acids were partitioned toward oxidation in the LIV0APOLY cells than in primary hepatocytes. LIV0APOLY cells offer the potential to be a renewable cellular model for studying the effects of exogenous metabolic substrates on fatty acid partitioning; however, their usefulness as a model of lipoprotein metabolism needs to be further explored.

Indexed as

Lipid MetabolismAcyltransferasesCell LineEndoplasmic Reticulum StressFatty AcidsGlucoseHepatocytesHep G2 CellsHumansInsulinLipaseLiverMembrane ProteinsNon-alcoholic Fatty Liver DiseasePhospholipases A2, Calcium-IndependentPhosphorylationAcyltransferasesFatty AcidsGlucoseInsulinLipaseMembrane ProteinsPhospholipases A2, Calcium-IndependentPNPLA3 protein, humanProto-Oncogene Proteins c-aktTriglycerideshepatocytehumanNAFLDPNPLA3triglyceride

Identifiers

PMID26126685
PMCPMC4572456
OpenAlexW2225549716

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.