Evidence map›Paper›PMID 24639359›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2014

Hepatic stellate cells orchestrate clearance of necrotic cells in a hypoxia-inducible factor-1α-dependent manner by modulating macrophage phenotype in mice.

Akie Mochizuki, Aaron Pace, Cheryl E Rockwell, Katherine J Roth, Aaron Chow, Kate M O'Brien, Ryan Albee, Kara Kelly, Keara Towery, James P Luyendyk and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

31 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Responses of hepatic sinusoidal cells to liver ischemia-reperfusion injury.Frontiers in cell and developmental biology · 2023
    Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. Hypoxia-inducible factors and innate immunity in liver cancer.The Journal of clinical investigation · 2020
    Review
  14. Article
  15. Review
  16. Fibrotic liver has prompt recovery after ischemia-reperfusion injury.American journal of physiology. Gastrointestinal and liver physiology · 2020
    Article
  17. Hepatic Macrophages in Liver Injury.Frontiers in immunology · 2020
    Review
  18. Article
  19. Review
  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

11 authors at 1 institution in 1 country.

Akie Mochizuki *Department of Pharmacology and Toxicology Michigan State University, East Lansing, MI 48824.
Aaron Pace *Department of Pharmacology and Toxicology Michigan State University, East Lansing, MI 48824.
Cheryl E RockwellDepartment of Pharmacology and Toxicology Michigan State University, East Lansing, MI 48824.
Katherine J RothDepartment of Pharmacology and Toxicology Michigan State University, East Lansing, MI 48824.
Aaron ChowDepartment of Pharmacology and Toxicology Michigan State University, East Lansing, MI 48824.
Kate M O'BrienDepartment of Pharmacology and Toxicology Michigan State University, East Lansing, MI 48824.
Ryan AlbeeDepartment of Pharmacology and Toxicology Michigan State University, East Lansing, MI 48824.
Kara KellyDepartment of Pharmacology and Toxicology Michigan State University, East Lansing, MI 48824.
Keara ToweryDepartment of Pathobiology and Diagnostic Investigation Michigan State University, East Lansing, MI 48824.
James P LuyendykDepartment of Pathobiology and Diagnostic Investigation Michigan State University, East Lansing, MI 48824.
Bryan L CoppleDepartment of Pharmacology and Toxicology Michigan State University, East Lansing, MI 48824.
Michigan State University · US

Funding

MULTIDISCIPLINARY TRAINING IN ENVIRONMENTAL TOXICOLOGYT32ES007255 · NIEHS · MICHIGAN STATE UNIVERSITY · PI JOHN J LAPRES · 1989 to 2026
$9.3M
Novel anti-fibrotic mechanisms in chemical-induced liver injuryR01ES017537 · NIEHS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI LUYENDYK, JAMES P · 2009 to 2019
$3.6M
Role of Early Growth Response Factor-1 in Cholestatic Liver InjuryR01DK073566 · NIDDK · UNIVERSITY OF KANSAS MEDICAL CENTER · PI COPPLE, BRYAN L · 2007 to 2017
$2.4M
Role of Nrf2 in immunotoxicity by food additives and environmental contaminantsR00ES018885 · NIEHS · MICHIGAN STATE UNIVERSITY · PI ROCKWELL, CHERYL ELIZABETH · 2012 to 2014
$740k
RISK MANAGEMENT IN NATIVE AMERICAN COMMUNITIESR25ES007255 · NIEHS · CLARK UNIVERSITY (WORCESTER, MA) · PI GOBLE, ROBERT L · 1994 to 2002
$738k
Role of Nrf2 in immunotoxicity by food additives and environmental contaminantsK99ES018885 · NIEHS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI ROCKWELL, CHERYL ELIZABETH · 2010 to 2011
$176k
NIDDK NIH HHS DK073566NIDDK NIH HHS R01 DK073566NIEHS NIH HHS ES017537NIEHS NIH HHS ES01888NIEHS NIH HHS K99 ES018885NIEHS NIH HHS R00 ES018885NIEHS NIH HHS R01 ES017537NIEHS NIH HHS R25 ES007255NIEHS NIH HHS T32 ES007255NIEHS NIH HHS T32ES007255
6 · The paper itself

Abstract

Hypoxia-inducible factor-1α (HIF-1α) is activated in hepatic stellate cells (HSCs) by hypoxia and regulates genes important for tissue repair. Whether HIF-1α is activated in HSCs after acute injury and contributes to liver regeneration, however, is not known. To investigate this, mice were generated with reduced levels of HIF-1α in HSCs by crossing HIF-1α floxed mice with mice that express Cre recombinase under control of the glial fibrillary acidic protein (GFAP) promoter (i.e., HIF-1α-GFAP Cre+ mice). These mice and control mice (i.e., HIF-1α-GFAP Cre- mice) were treated with a single dose of carbon tetrachloride, and liver injury and repair were assessed. After carbon tetrachloride, HIF-1α was activated in HSCs. Although liver injury was not different between the two strains of mice, during resolution of injury, clearance of necrotic cells was decreased in HIF-1α-GFAP Cre+ mice. In these mice, the persistence of necrotic cells stimulated a fibrotic response characterized by extensive collagen deposition. Hepatic accumulation of macrophages, which clear necrotic cells from the liver after carbon tetrachloride, was not affected by HIF-1α deletion in HSCs. Conversion of macrophages to M1-like, proinflammatory macrophages, which have increased phagocytic activity, however, was reduced in HIF-1α-GFAP Cre+ mice as indicated by a decrease in proinflammatory cytokines and a decrease in the percentage of Gr1(hi) macrophages. Collectively, these studies have identified a novel function for HSCs and HIF-1α in orchestrating the clearance of necrotic cells from the liver and demonstrated a key role for HSCs in modulating macrophage phenotype during acute liver injury.

Indexed as

PhenotypeAnimalsCarbon TetrachlorideCell ProliferationChemical and Drug Induced Liver InjuryGene DeletionHepatic Stellate CellsHepatocytesHypoxia-Inducible Factor 1, alpha SubunitLiver CirrhosisMacrophagesMiceMice, TransgenicNecrosisNeutrophilsUrokinase-Type Plasminogen ActivatorCarbon TetrachlorideHypoxia-Inducible Factor 1, alpha SubunitUrokinase-Type Plasminogen Activator

Identifiers

PMID24639359
PMCPMC4538924
OpenAlexW2119330243

What OpenQuestion holds

Textmetadata
LicenceTDM
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.