Evidence map›Paper›PMID 23125524›Full record

ReviewJournal of biomedicine & biotechnology2012

The plasminogen receptor, Plg-R(KT), and macrophage function.

Lindsey A Miles, Shahrzad Lighvani, Nagyung Baik, Nicholas M Andronicos, Emily I Chen, Caitlin M Parmer, Sophia Khaldoyanidi, Jenna E Diggs, William B Kiosses, Mark P Kamps and 2 more

Open access · hybridAbstract readReview
In one paragraph

Review in Journal of biomedicine & biotechnology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Dietary Inclusion of Seabuckthorn (Frontiers in physiology · 2022
    Article
  4. Review
  5. The plasminogen receptor, Plg-RCell death & disease · 2020
    Article
  6. Article
  7. Functions of the plasminogen receptor Plg-RJournal of thrombosis and haemostasis : JTH · 2020
    Review
  8. Article
  9. Article
  10. Podocyte injury: the role of proteinuria, urinary plasminogen, and oxidative stress.American journal of physiology. Renal physiology · 2016
    Article
  11. Article
  12. New insights into the role of Plg-RKT in macrophage recruitment.International review of cell and molecular biology · 2014
    Review
  13. Plasminogen receptors: the first quarter century.Seminars in thrombosis and hemostasis · 2013
    Review
  14. 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

12 authors at 6 institutions in 2 countries.

Lindsey A MilesDepartment of Cell Biology, The Scripps Research Institute, 10550 N. Torrey Pines Road, SP30-3020, La Jolla, CA 92037, USA.
Shahrzad Lighvani
Nagyung Baik
Nicholas M Andronicos
Emily I Chen
Caitlin M Parmer
Sophia Khaldoyanidi
Jenna E Diggs
William B Kiosses
Mark P Kamps
John R Yates
Robert J Parmer
Scripps Research Institute · USUniversity of California, San Diego · USCommonwealth Scientific and Industrial Research Organisation · AUStony Brook University · USTorrey Pines Institute For Molecular Studies · USYale University · US

Funding

ZDS2P REGULATES SWE1P-DEPENDENT POLARIZED CELL GROWTH IN S CEREVISIAEP41RR011823 · NCRR · UNIVERSITY OF WASHINGTON · PI SALVESEN, GUY S. · 1996 to 2011
$24.7M
TrainingP41GM103533 · NIGMS · UNIVERSITY OF WASHINGTON · PI MACCOSS, MICHAEL · 2012 to 2021
$20.7M
Regulation of plasminogen-dependent cell functions by the novel receptor, Plg-RKTR01HL081046 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI MILES, LINDSEY A · 2007 to 2024
$8.7M
REGULATION OF THE PLASMINOGEN SYSTEMR01HL045934 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI MILES, LINDSEY A · 1990 to 2006
$2.5M
REGULATION OF FIBRINOLYSIS BY CELL SURFACESR01HL038272 · NHLBI · SCRIPPS RESEARCH INSTITUTE · PI MILES, LINDSEY A · 1994 to 2002
$961k
PROCESSING OF CHROMOGRANIN A BY THE FIBRINOLYTIC SYSTEMR01HL050398 · NHLBI · VETERANS MEDICAL RESEARCH FDN/SAN DIEGO · PI PARMER, ROBERT J · 1994 to 2001
$424k
REGULATION OF FIBRINOLYSIS BY CELL SURFACESR29HL038272 · NHLBI · SCRIPPS RESEARCH INSTITUTE · PI MILES, LINDSEY A · 1988 to 1992
–
NCRR NIH HHS P41 RR011823NHLBI NIH HHS HL081046NHLBI NIH HHS HL38272NHLBI NIH HHS HL45934NHLBI NIH HHS HL50398NHLBI NIH HHS R01 HL038272NHLBI NIH HHS R01 HL045934NHLBI NIH HHS R01 HL050398NHLBI NIH HHS R01 HL081046NIGMS NIH HHS GM103533NIGMS NIH HHS P41 GM103533
6 · The paper itself

Abstract

When plasminogen binds to cells its activation to plasmin is markedly enhanced compared to the reaction in solution. Thus, cells become armed with the broad spectrum proteolytic activity of plasmin. Cell-surface plasmin plays a key role in macrophage recruitment during the inflammatory response. Proteins exposing basic residues on the cell surface promote plasminogen activation on eukaryotic cells. We have used a proteomics approach combining targeted proteolysis with carboxypeptidase B and multidimensional protein identification technology, MudPIT, and a monocyte progenitor cell line to identify a novel transmembrane protein, the plasminogen receptor, Plg-R(KT). Plg-R(KT) exposes a C-terminal lysine on the cell surface in an orientation to bind plasminogen and promote plasminogen activation. Here we review the characteristics of this new protein, with regard to membrane topology, conservation of sequence across species, the role of its C-terminus in plasminogen binding, its function in plasminogen activation, cell migration, and its role in macrophage recruitment in the inflammatory response.

Indexed as

Amino Acid SequenceAnimalsConserved SequenceHumansInflammationLysineMacrophagesMolecular Sequence DataPlasminogenReceptors, Urokinase Plasminogen ActivatorLysinePlasminogenReceptors, Urokinase Plasminogen Activator

Identifiers

PMID23125524
PMCPMC3484331
OpenAlexW2159342953

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.