Evidence map›Paper›PMID 19500591›Full record

ArticleJournal of molecular biology2009

Solution characterization of the extracellular region of CD147 and its interaction with its enzyme ligand cyclophilin A.

Jennifer Schlegel, Jasmina S Redzic, Christopher C Porter, Vyacheslav Yurchenko, Michael Bukrinsky, Wladimir Labeikovsky, Geoffrey S Armstrong, Fengli Zhang, Nancy G Isern, James DeGregori and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of molecular biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

44 citing papers in PubMed, 73 citations in OpenAlex.

  1. Review
  2. Article
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  4. Article
  5. Article
  6. Article
  7. Cyclophilin A/CD147 Interaction: A Promising Target for Anticancer Therapy.International journal of molecular sciences · 2022
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
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  14. Article
  15. Article
  16. Interleukin-37 monomer is the active form for reducing innate immunity.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  17. Article
  18. Review
  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

12 authors at 7 institutions in 1 country.

Jennifer SchlegelDepartment of Biochemistry and Molecular Genetics, University of Colorado Denver, School of Medicine, Aurora, CO 80045, USA.
Jasmina S Redzic
Christopher C Porter
Vyacheslav Yurchenko
Michael Bukrinsky
Wladimir Labeikovsky
Geoffrey S Armstrong
Fengli Zhang
Nancy G Isern
James DeGregori
Robert Hodges
Elan Zohar Eisenmesser
University of Colorado Denver · USAlbert Einstein College of Medicine · USEnvironmental Molecular Sciences Laboratory · USGeorge Washington University · USNational High Magnetic Field Laboratory · USRockefeller University · USUniversity of Colorado Boulder · US

Funding

Purchase of 900 MHz NMR SpectrometerP41GM068928 · NIGMS · UNIVERSITY OF COLORADO AT BOULDER · PI WUTTKE, DEBORAH S. · 2003 to 2009
$6.4M
POSTGRADUATE TRAINING IN PEDIATRIC ONCOLOGYT32CA082086 · NCI · UNIVERSITY OF COLORADO DENVER · PI GORE, LIA · 2000 to 2015
$4.1M
Poor competition in hematopoietic stem/progenitor pools favors tumorigenesisR01CA109657 · NCI · UNIVERSITY OF COLORADO DENVER · PI DEGREGORI, JAMES V · 2005 to 2009
$1.1M
Cyclophilin-CD147 interaction in autoimmune arthritisR56AI081152 · NIAID · GEORGE WASHINGTON UNIVERSITY · PI BUKRINSKY, MICHAEL ILYA, CONSTANT, STEPHANIE L · 2009 to 2010
$783k
Leukocyte recruitment by cyclophilin-CD147 interactionR21AI060720 · NIAID · GEORGE WASHINGTON UNIVERSITY · PI BUKRINSKY, MICHAEL ILYA · 2004 to 2005
$421k
NCI NIH HHS R01 CA109657NCI NIH HHS T32 CA082086NIAID NIH HHS R01 AI081152NIAID NIH HHS R21 AI060720NIAID NIH HHS R56 AI081152NIGMS NIH HHS GM68928
6 · The paper itself

Abstract

The CD147 receptor plays an integral role in numerous diseases by stimulating the expression of several protein families and serving as the receptor for extracellular cyclophilins; however, neither CD147 nor its interactions with its cyclophilin ligands have been well characterized in solution. CD147 is a unique protein in that it can function both at the cell membrane and after being released from cells where it continues to retain activity. Thus, the CD147 receptor functions through at least two mechanisms that include both cyclophilin-independent and cyclophilin-dependent modes of action. In regard to CD147 cyclophilin-independent activity, CD147 homophilic interactions are thought to underlie its activity. In regard to CD147 cyclophilin-dependent activity, cyclophilin/CD147 interactions may represent a novel means of signaling since cyclophilins are also peptidyl-prolyl isomerases. However, direct evidence of catalysis has not been shown within the cyclophilin/CD147 complex. In this report, we have characterized the solution behavior of the two most prevalent CD147 extracellular isoforms through biochemical methods that include gel-filtration and native gel analysis as well as directly through multiple NMR methods. All methods indicate that the extracellular immunoglobulin-like domains are monomeric in solution and, thus, suggest that CD147 homophilic interactions in vivo are mediated through other partners. Additionally, using multiple NMR techniques, we have identified and characterized the cyclophilin target site on CD147 and have shown for the first time that CD147 is also a substrate of its primary cyclophilin enzyme ligand, cyclophilin A.

Indexed as

Protein FoldingBasiginCatalysisCyclophilin AHumansModels, MolecularProtein BindingProtein IsoformsProtein Structure, SecondaryProtein Structure, TertiaryRecombinant ProteinsSyndecan-1BasiginCyclophilin AProtein IsoformsRecombinant ProteinsSDC1 protein, humanSyndecan-1

Identifiers

PMID19500591
PMCPMC2940942
OpenAlexW2077426548

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.