Evidence map›Paper›PMID 25342128›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2015

Heme oxygenase-2 deletion impairs macrophage function: implication in wound healing.

Lars Bellner, Giuseppina Marrazzo, Nico van Rooijen, Michael W Dunn, Nader G Abraham, Michal L Schwartzman

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

28 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Therapeutic Potential ofAntioxidants (Basel, Switzerland) · 2023
    Article
  5. Heme-heme oxygenase-2 reduces the atherosclerosis by preventing inflammation.Current research in pharmacology and drug discovery · 2023
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Antioxidants (Basel, Switzerland) · 2021
    Article
  11. Article
  12. Review
  13. Article
  14. The Human Tissue-Engineered Cornea (hTEC): Recent Progress.International journal of molecular sciences · 2021
    Review
  15. Plasmacytoid dendritic cells in the eye.Progress in retinal and eye research · 2021
    Review
  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

6 authors at 2 institutions in 2 countries.

Lars BellnerDepartment of Pharmacology, lars_bellner@nymc.edu.
Giuseppina MarrazzoDepartment of Pharmacology.
Nico van RooijenDepartment of Molecular Cell Biology, Faculty of Medicine, Vrije Universiteit, Amsterdam, The Netherlands.
Michael W DunnDepartment of Ophthalmology, and.
Nader G AbrahamDepartment of Pharmacology, Department of Medicine, New York Medical College, Valhalla, New York, USA; and.
Michal L SchwartzmanDepartment of Pharmacology, Department of Ophthalmology, and.
New York Medical College · USVrije Universiteit Amsterdam · NL

Funding

Vasoregulatory Function of CYP2E1-Derived EicosanoidsP01HL034300 · NHLBI · NEW YORK MEDICAL COLLEGE · PI JIANG, HOULI · 1985 to 2015
$33.4M
CORNEAL ARACHIDONATE METABOLITES VIA CYTOCHROME P450R01EY006513 · NEI · NEW YORK MEDICAL COLLEGE · PI SCHWARTZMAN, MICHAL LANIADO · 1987 to 2010
$4.2M
NEI NIH HHS R01 EY006513NEI NIH HHS R01EY06513NHLBI NIH HHS P01 HL034300
6 · The paper itself

Abstract

Heme oxygenase (HO)-2 deficiency impairs wound healing and exacerbates inflammation following injury. We examine the impact of HO-2 deficiency on macrophage function and the contribution of macrophage HO-2 to inflammatory and repair responses to injury. Corneal epithelial debridement was performed in control and macrophage-depleted HO-2(-/-) and wild-type (WT) mice and in bone marrow chimeras. Peritoneal macrophages were collected for determination of phagocytic activity and classically activated macrophage (M1)-alternatively activated macrophage (M2) polarization. Depletion of macrophages delayed corneal healing (13.2%) and increased neutrophil infiltration (54.1%) by day 4 in WT mice, whereas in HO-2(-/-) mice, it did not worsen the already impaired wound healing and exacerbated inflammation. HO-2(-/-) macrophages displayed an altered M1 phenotype with no significant expression of M2 or M2-like activated cells and a 31.3% reduction in phagocytic capacity that was restored by inducing HO-1 activity or supplementing biliverdin. Macrophage depletion had no effect, whereas adoptive transfer of WT bone marrow improved wound healing (34% on day 4) but did not resolve the exaggerated inflammatory response in HO-2(-/-) mice. These findings indicate that HO-2-deficient macrophages are dysfunctional and that macrophage HO-2 is required for proper macrophage function but is insufficient to correct the impaired healing of the HO-2(-/-) cornea, suggesting that corneal epithelial expression of HO-2 is a key to resolution and repair in wound healing.

Indexed as

AnimalsBone Marrow TransplantationCorneal InjuriesCytokinesEpithelium, CornealFemaleHeme Oxygenase-1Heme Oxygenase (Decyclizing)InflammationMacrophage ActivationMacrophagesMiceMice, 129 StrainMice, Inbred C57BLMice, KnockoutNeutrophil InfiltrationCytokinesHeme Oxygenase-1heme oxygenase-2Heme Oxygenase (Decyclizing)RNA, Messengerbone marrow transferclodronate liposomesinflammation

Identifiers

PMID25342128
PMCPMC4285548
OpenAlexW2062526438

What OpenQuestion holds

Textmetadata
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.