Evidence map›Paper›PMID 17071586›Full record

ArticleThe American journal of pathology2006

Dual role for plasminogen activator inhibitor type 1 as soluble and as matricellular regulator of epithelial alveolar cell wound healing.

François Maquerlot, Stephane Galiacy, Michel Malo, Christophe Guignabert, Daniel A Lawrence, Maria-Pia d'Ortho, Georgia Barlovatz-Meimon

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

22 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
  2. Article
  3. Molecular biomarkers of Graves' ophthalmopathy.Experimental and molecular pathology · 2019
    Review
  4. Review
  5. Review
  6. Article
  7. Oxidative Stress and Skin Fibrosis.Current pathobiology reports · 2014
    Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Epithelial repair mechanisms in the lung.American journal of physiology. Lung cellular and molecular physiology · 2010
    Review
  15. Article
  16. Article
  17. Matricellular proteins: an overview.Journal of cell communication and signaling · 2009
    Article
  18. Article
  19. Article
  20. uPA dependent and independent mechanisms of wound healing by C-phycocyanin.Journal of cellular and molecular medicine · 2008
    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

7 authors at 4 institutions in 2 countries.

François MaquerlotInformatique, Biologie Intégrative et Systèmes Complexes, FRE 2873 Centre National de la Recherche Scientifique, Université d'Evry, Génopole, Evry, France.
Stephane Galiacy
Michel Malo
Christophe Guignabert
Daniel A Lawrence
Maria-Pia d'Ortho
Georgia Barlovatz-Meimon
Centre National de la Recherche Scientifique · FRInserm · FRDuke University · USUniversity of Michigan · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epithelium repair, crucial for restoration of alveolo-capillary barrier integrity, is orchestrated by various cytokines and growth factors. Among them keratinocyte growth factor plays a pivotal role in both cell proliferation and migration. The urokinase plasminogen activator (uPA) system also influences cell migration through proteolysis during epithelial repair. In addition, the complex formed by uPAR-uPA and matrix-bound plasminogen activator inhibitor type-1 (PAI-1) exerts nonproteolytic roles in various cell types. Here we present new evidence about the dual role of PAI-1 under keratinocyte growth factor stimulation using an in vitro repair model of rat alveolar epithelial cells. Besides proteolytic involvement of the uPA system, the availability of matrix-bound-PAI-1 is also required for an efficient healing. An unexpected decrease of healing was shown when PAI-1 activity was blocked. However, the proteolytic action of uPA and plasmin were still required. Moreover, immediately after wounding, PAI-1 was dramatically increased in the newly deposited matrix at the leading edge of wounds. We thus propose a dual role for PAI-1 in epithelial cell wound healing, both as a soluble inhibitor of proteolysis and also as a matrix-bound regulator of cell migration. Matrix-bound PAI-1 could thus be considered as a new member of the matricellular protein family.

Indexed as

AnimalsEpithelial CellsExtracellular MatrixFibrinolysinFibroblast Growth Factor 7MaleModels, BiologicalPlasminogen Activator Inhibitor 1Protein TransportPulmonary AlveoliRatsRats, Sprague-DawleySolubilityUrokinase-Type Plasminogen ActivatorWound HealingFibrinolysinFibroblast Growth Factor 7Plasminogen Activator Inhibitor 1Urokinase-Type Plasminogen Activator

Identifiers

PMID17071586
PMCPMC1780203
OpenAlexW2040967348

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.