Evidence map›Paper›PMID 25273880›Full record

ArticleAmerican journal of physiology. Cell physiology2014

Neuroprotectin/protectin D1: endogenous biosynthesis and actions on diabetic macrophages in promoting wound healing and innervation impaired by diabetes.

Song Hong, Haibin Tian, Yan Lu, James Monroe Laborde, Filipe A Muhale, Quansheng Wang, Bhagwat V Alapure, Charles N Serhan, Nicolas G Bazan

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
4.9field-weighted citation impact, top 5% 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

33 citing papers in PubMed, 52 citations in OpenAlex.

  1. Plasma Resolvin D2 to Leukotriene BBioMed research international · 2021
    Trial
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Novel lipid mediator 7Frontiers in cell and developmental biology · 2024
    Article
  8. Article
  9. Article
  10. Maresin-2 promotes mucosal repair and has therapeutic potential when encapsulated in thermostable nanoparticles.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Eicosanoids in Skin Wound Healing.International journal of molecular sciences · 2020
    Review
  16. Article
  17. Article
  18. Article
  19. Omega 3 Fatty Acid and Skin Diseases.Frontiers in immunology · 2020
    Review
  20. Dynamics of the human skin mediator lipidome in response to dietary ω-3 fatty acid supplementation.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    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

9 authors at 2 institutions in 1 country.

Song HongNeuroscience Center of Excellence, Louisiana State University Health Sciences Center, New Orleans, Louisiana; Department of Ophthalmology, Louisiana State University Health Sciences Center, New Orleans, Louisiana; shong@lsuhsc.edu.
Haibin TianNeuroscience Center of Excellence, Louisiana State University Health Sciences Center, New Orleans, Louisiana;
Yan LuNeuroscience Center of Excellence, Louisiana State University Health Sciences Center, New Orleans, Louisiana;
James Monroe LabordeDepartment of Orthopedic Surgery, Louisiana State University Health Sciences Center, New Orleans, Louisiana; and.
Filipe A MuhaleNeuroscience Center of Excellence, Louisiana State University Health Sciences Center, New Orleans, Louisiana;
Quansheng WangNeuroscience Center of Excellence, Louisiana State University Health Sciences Center, New Orleans, Louisiana;
Bhagwat V AlapureNeuroscience Center of Excellence, Louisiana State University Health Sciences Center, New Orleans, Louisiana;
Charles N SerhanCenter for Experimental Therapeutics and Reperfusion Injury, Brigham and Women's Hospital; Department of Anaesthesia (Biochemistry and Molecular Pharmacology), Harvard Medical School; Department of Oral Medicine, Infection and Immunity, Harvard School of Dental Medicine, Boston, Massachusetts.
Nicolas G BazanNeuroscience Center of Excellence, Louisiana State University Health Sciences Center, New Orleans, Louisiana; Department of Ophthalmology, Louisiana State University Health Sciences Center, New Orleans, Louisiana;
Louisiana State University Health Sciences Center New Orleans · USHarvard University · US

Funding

Resolution Mechanisms in Acute Inflammation: Resolution PharmacologyP01GM095467 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI SERHAN, CHARLES NICHOLAS · 2011 to 2020
$14.8M
Multiphoton ConfocalP30GM103340 · NIGMS · LSU HEALTH SCIENCES CENTER · PI BAZAN, NICOLAS G. · 2012 to 2016
$5.1M
PROHEALING LIPID AUTOCRINES PARACRINES OF MACROPHAGES AND NERVES IN DIABETIC WOUND RE-INNERVATION - NANOPARTICLE-SUSTAINED RELEASER01DK087800 · NIDDK · LSU HEALTH SCIENCES CENTER · PI HONG, SONG · 2010 to 2018
$2.3M
NIDDK NIH HHS R01 DK087800NIDDK NIH HHS R01-DK-087800NIGMS NIH HHS 1P01 GM-095467NIGMS NIH HHS P01 GM095467NIGMS NIH HHS P30-GM-103340
6 · The paper itself

Abstract

Dysfunction of macrophages (MΦs) in diabetic wounds impairs the healing. MΦs produce anti-inflammatory and pro-resolving neuroprotectin/protectin D1 (NPD1/PD1, 10R,17S-dihydroxy-docosa-4Z,7Z,11E,13E,15Z,19Z-hexaenoic acid); however, little is known about endogenous NPD1 biosynthesis by MΦs and the actions of NPD1 on diabetic MΦ functions in diabetic wound healing. We used an excisional skin wound model of diabetic mice, MΦ depletion, MΦs isolated from diabetic mice, and mass spectrometry-based targeted lipidomics to study the time course progression of NPD1 levels in wounds, the roles of MΦs in NPD1 biosynthesis, and NPD1 action on diabetic MΦ inflammatory activities. We also investigated the healing, innervation, chronic inflammation, and oxidative stress in diabetic wounds treated with NPD1 or NPD1-modulated MΦs from diabetic mice. Injury induced endogenous NPD1 biosynthesis in wounds, but diabetes impeded NPD1 formation. NPD1 was mainly produced by MΦs. NPD1 enhanced wound healing and innervation in diabetic mice and promoted MΦs functions that accelerated these processes. The underlying mechanisms for these actions of NPD1 or NPD1-modulated MΦs involved 1) attenuating MΦ inflammatory activities and chronic inflammation and oxidative stress after acute inflammation in diabetic wound, and 2) increasing MΦ production of IL10 and hepatocyte growth factor. Taken together, NPD1 appears to be a MΦs-produced factor that accelerates diabetic wound healing and promotes MΦ pro-healing functions in diabetic wounds. Decreased NPD1 production in diabetic wound is associated with impaired healing. This study identifies a new molecular target that might be useful in development of more effective therapeutics based on NPD1 and syngeneic diabetic MΦs for treatment of diabetic wounds.

Indexed as

AnimalsCells, CulturedDiabetes ComplicationsDiabetes Mellitus, Type 2Docosahexaenoic AcidsGene Expression RegulationInflammationMacrophagesMiceMolecular StructureOxidative StressSkinWound HealingWounds and InjuriesDocosahexaenoic Acidsprotectin D1anti-inflammatory and pro-resolving mediatorsdiabetic wound healingmacrophagepro-healing and neurotrophic function

Identifiers

PMID25273880
PMCPMC4254953
OpenAlexW2127060795

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.