Evidence map›Paper›PMID 12102655›Full record

ArticleThe Biochemical journal2002

Binding of C-reactive protein to modified low-density-lipoprotein particles: identification of cholesterol as a novel ligand for C-reactive protein.

Sanna Taskinen, Petri T Kovanen, Hanna Jarva, Seppo Meri, Markku O Pentikäinen

Open access · bronzeAbstract read
In one paragraph

Article in The Biochemical journal, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.9field-weighted citation impact, top 5% 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

20 citing papers in PubMed, 66 citations in OpenAlex.

  1. Review
  2. Review
  3. An overview onHeliyon · 2020
    Review
  4. Review
  5. Review
  6. Article
  7. Atherosclerosis-related functions of C-reactive protein.Cardiovascular & hematological disorders drug targets · 2010
    Article
  8. Article
  9. Article
  10. CRP and the risk of atherosclerotic events.Seminars in immunopathology · 2009
    Review
  11. Pattern recognition by pentraxins.Advances in experimental medicine and biology · 2009
    Review
  12. Article
  13. Article
  14. Review
  15. Physical activity and high-sensitivity C-reactive protein.Sports medicine (Auckland, N.Z.) · 2006
    Review
  16. Article
  17. CRP after 2004.Molecular immunology · 2005
    Review
  18. Review
  19. Article
  20. Oxidized phosphatidylcholines: pattern recognition ligands for multiple pathways of the innate immune response.Proceedings of the National Academy of Sciences of the United States of America · 2002
    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

5 authors at 2 institutions in 1 country.

Sanna TaskinenWihuri Research Institute, Kalliolinnantie 4, FIN-00140 Helsinki, Finland.
Petri T Kovanen
Hanna Jarva
Seppo Meri
Markku O Pentikäinen
Wihuri Research Institute · FIUniversity of Helsinki · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

C-reactive protein (CRP), an acute-phase reactant, is present in atherosclerotic human arterial intima in association with lipids. In the present work we studied interactions between CRP and LDL on microtitre wells, where either CRP or LDL was immobilized. LDL was modified by vortex-mixing, oxidation, or by lipolysis with phospholipase A(2) or with sphingomyelinase or a combination of trypsin and cholesterol esterase. We found that CRP bound only to LDL modified by trypsin/cholesterol esterase or by sphingomyelinase and that this binding was Ca(2+)-dependent. In these two forms of modified LDL, non-esterified cholesterol was susceptible to cholesterol oxidase, indicating exposure of non-esterified cholesterol on particle surfaces and suggesting a role for non-esterified cholesterol in mediating CRP binding. Consistent with this hypothesis were the following findings: (i) increasing the amount of non-esterified cholesterol in LDL with cyclodextrin increased, and decreasing its amount decreased, the binding of CRP to LDL; (ii) modification of non-esterified cholesterol in LDL by cholesterol oxidase decreased the binding of CRP to LDL; and (iii) CRP bound to purified non-esterified cholesterol. The binding was Ca(2+)-dependent and could be competed out with phosphocholine. Taken together, these findings suggest that CRP can bind to modified lipoproteins, notably to the non-esterified cholesterol on their surface. These interactions may be related to the suggested role of CRP in the local inflammation present in atherosclerotic plaques.

Indexed as

ArteriosclerosisCalciumCholesterolC-Reactive ProteinCyclodextrinsHumansLigandsLipoproteins, LDLOxidation-ReductionPhosphatidylcholinesPhospholipases ASphingomyelin PhosphodiesteraseSterol EsteraseTrypsinCalciumCholesterolC-Reactive ProteinCyclodextrinsLigandsLipoproteins, LDLPhosphatidylcholinesPhospholipases ASphingomyelin PhosphodiesteraseSterol EsteraseTrypsin

Identifiers

PMID12102655
PMCPMC1222894
OpenAlexW2010826690

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.