Evidence map›Paper›PMID 7615819›Full record

ArticleThe Journal of clinical investigation1995

Urokinase receptor is a multifunctional protein: influence of receptor occupancy on macrophage gene expression.

N K Rao, G P Shi, H A Chapman

Open access · hybridAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1995. 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
4.7field-weighted citation impact, top 4% 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, 70 citations in OpenAlex.

  1. Preclinical Evaluation of aACS pharmacology & translational science · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Proteases and glioma angiogenesis.Brain pathology (Zurich, Switzerland) · 2005
    Review
  10. Article
  11. Induction of the plasminogen activator system accompanies peripheral nerve regeneration after sciatic nerve crush.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2001
    Article
  12. Mice lacking tPA, uPA, or plasminogen genes showed delayed functional recovery after sciatic nerve crush.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2001
    Article
  13. Article
  14. Article
  15. Hypotension and inflammatory cytokine gene expression triggered by factor Xa-nitric oxide signaling.Proceedings of the National Academy of Sciences of the United States of America · 1998
    Article
  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

3 authors at 1 institution in 1 country.

N K RaoDivision of Biological Sciences, Harvard School of Public Health, Boston, Massachusetts, USA.
G P Shi
H A Chapman
Massachusetts Department of Public Health · US

Funding

PHS HHS 48261
6 · The paper itself

Abstract

Binding of urokinase to the glycolipid-anchored urokinase receptor (uPAR) has been implicated in macrophage differentiation. However, no biochemical markers of differentiation have yet been directly linked to uPAR occupancy. As extensive changes in proteolytic profile characterize monocytic differentiation, we have examined the role of uPAR occupancy on protease expression by differentiating phagocytes. Antibodies to either urokinase or to uPAR that prevent receptor binding inhibited induction of cathepsin B in cultured monocytes and both cathepsin B and 92-kD gelatinase mRNA and protein in phorbol diester-stimulated myeloid cells. Mannosamine, an inhibitor of glycolipid anchor assembly, also blocked protease expression. Anti-catalytic urokinase antibodies, excess inactive urokinase, or aprotinin had no effect, indicating that receptor occupancy per se regulated protease expression. Antibodies to the integrins CD11a and CD29 or to the glycolipid-anchored proteins CD14 and CD55 also had no effect. Protease induction was independent of matrix attachment. Antibodies to urokinase or uPAR affected neither the decrease in cathepsin G nor the increase in tumor necrosis factor-alpha in phorbol ester-stimulated cells. These data establish that uPAR is a multifunctional receptor, not only promoting pericellular proteolysis and matrix attachment, but also effecting cysteine- and metallo-protease expression during macrophage differentiation.

Indexed as

Gene ExpressionCathepsin BCell AdhesionCells, CulturedCollagenasesGlycosylphosphatidylinositolsHumansMacrophagesMatrix Metalloproteinase 9Receptors, Cell SurfaceReceptors, Urokinase Plasminogen ActivatorTetradecanoylphorbol AcetateTumor Necrosis Factor-alphaCathepsin BCollagenasesGlycosylphosphatidylinositolsMatrix Metalloproteinase 9PLAUR protein, humanReceptors, Cell SurfaceReceptors, Urokinase Plasminogen ActivatorTetradecanoylphorbol AcetateTumor Necrosis Factor-alpha

Identifiers

PMID7615819
PMCPMC185220
OpenAlexW2000723452

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.