Evidence map›Paper›PMID 25383879›Full record

ArticlePloS one2014

Nerve growth factor regulates neurolymphatic remodeling during corneal inflammation and resolution.

Darci M Fink, Alicia L Connor, Philip M Kelley, Maria M Steele, Michael A Hollingsworth, Richard M Tempero

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.3field-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

16 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Roles of growth factors in eye development and ophthalmic diseases.Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2022
    Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. NGF (-198C > T, Ala35Val) and p75Molecular medicine (Cambridge, Mass.) · 2020
    Article
  9. Article
  10. NGF/anti-VEGF combined exposure protects RCS retinal cells and photoreceptors that underwent a local worsening of inflammation.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2017
    Article
  11. Article
  12. Review
  13. Article
  14. Lymphatic endothelial lineage assemblage during corneal lymphangiogenesis.Laboratory investigation; a journal of technical methods and pathology · 2016
    Article
  15. Human β-NGF gene transferred to cat corneal endothelial cells.International journal of ophthalmology · 2016
    Article
  16. 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 3 institutions in 1 country.

Darci M FinkUniversity of Nebraska Medical Center, Eppley Institute for Research in Cancer and Allied Diseases, 985950 Nebraska Medical Center, Omaha, Nebraska 68198-5950, United States of America.
Alicia L ConnorBoys Town National Research Hospital, Department of Genetics, 555 North 30th Street, Omaha, Nebraska 68131, United States of America.
Philip M KelleyBoys Town National Research Hospital, Department of Genetics, 555 North 30th Street, Omaha, Nebraska 68131, United States of America.
Maria M SteeleUniversity of Nebraska Medical Center, Eppley Institute for Research in Cancer and Allied Diseases, 985950 Nebraska Medical Center, Omaha, Nebraska 68198-5950, United States of America.
Michael A HollingsworthUniversity of Nebraska Medical Center, Eppley Institute for Research in Cancer and Allied Diseases, 985950 Nebraska Medical Center, Omaha, Nebraska 68198-5950, United States of America.
Richard M TemperoBoys Town National Research Hospital, Department of Genetics, 555 North 30th Street, Omaha, Nebraska 68131, United States of America; Boys Town National Research Hospital, Department of Otolaryngology, 555 North 30th Street, Omaha, Nebraska 68131, United States of America.
Boys Town National Research Hospital · USUniversity of Nebraska Medical Center · USNebraska Medical Center · US

Funding

UNMC/EPPLEY CANCER CENTER SUPPORT GRANTP30CA036727 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Apar Kishor Ganti · 1985 to 2026
$55.0M
Tissue CoreP50CA127297 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI HOLLINGSWORTH, MICHAEL A. · 2008 to 2018
$17.1M
TRANSGENIC EXPRESSION ANALYSIS OF MIRNA-144P20RR018788 · NCRR · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI WESTON, MICHAEL D · 2003 to 2011
$16.5M
CHEMICAL CARCINOGENESIS &CANCER BIOLOGYT32CA009476 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Jennifer D. Black · 1988 to 2026
$6.2M
UNMC Histology/Imaging and Creighton University Imaging Core FacilityP30GM110768 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI SMITH, SHELLEY D · 2014 to 2018
$5.1M
Role of N-Cadherin in Pancreatic Tumor MicroenvironmentU54CA163120 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI HOLLINGSWORTH, MICHAEL A. · 2011 to 2015
$4.2M
The Molecular Biology of Neurosurgery SystemsP20GM103471 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI SMITH, SHELLEY D · 2012 to 2013
$4.1M
INTEGRIN REGULATION OF CORNEAL LYMPHATIC VESSEL GROWTH AND REGRESSIONR01EY021571 · NEI · FATHER FLANAGAN'S BOYS' HOME · PI TEMPERO, RICHARD M. · 2012 to 2016
$1.5M
NCI NIH HHS P30 CA036727NCI NIH HHS P50 CA127297NCI NIH HHS T32 CA009476NCI NIH HHS U54 CA163120NCRR NIH HHS 5 P20 RR018788-08NCRR NIH HHS P20 RR018788NEI NIH HHS R01 EY021571NEI NIH HHS R01-EY021571NIGMS NIH HHS P20 GM103471NIGMS NIH HHS P30 GM110768
6 · The paper itself

Abstract

The cellular and physiologic mechanisms that regulate the resolution of inflammation remain poorly defined despite their widespread importance in improving inflammatory disease outcomes. We studied the resolution of two cardinal signs of inflammation-pain and swelling-by investigating molecular mechanisms that regulate neural and lymphatic vessel remodeling during the resolution of corneal inflammation. A mouse model of corneal inflammation and wound recovery was developed to study this process in vivo. Administration of nerve growth factor (NGF) increased pain sensation and inhibited neural remodeling and lymphatic vessel regression processes during wound recovery. A complementary in vivo approach, the corneal micropocket assay, revealed that NGF-laden pellets stimulated lymphangiogenesis and increased protein levels of VEGF-C. Adult human dermal lymphatic endothelial cells did not express canonical NGF receptors TrkA and p75NTR or activate downstream MAPK- or Akt-pathway effectors in the presence of NGF, although NGF treatment increased their migratory and tubulogenesis capacities in vitro. Blockade of the VEGF-R2/R3 signaling pathway ablated NGF-mediated lymphangiogenesis in vivo. These findings suggest a hierarchical relationship with NGF functioning upstream of the VEGF family members, particularly VEGF-C, to stimulate lymphangiogenesis. Taken together, these studies show that NGF stimulates lymphangiogenesis and that NGF may act as a pathogenic factor that negatively regulates the normal neural and lymphatic vascular remodeling events that accompany wound recovery.

Indexed as

Wound HealingAdultAnimalsCells, CulturedCorneaDisease Models, AnimalEndothelial CellsHumansInflammationMAP Kinase Signaling SystemMiceNerve Growth FactorNerve Tissue ProteinsReceptors, Nerve Growth FactorReceptor, trkANerve Growth FactorNerve Tissue ProteinsNGF protein, humanNGFR protein, humanReceptors, Nerve Growth FactorReceptor, trkA

Identifiers

PMID25383879
PMCPMC4226611
OpenAlexW2013876541

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.