Evidence map›Paper›PMID 18208975›Full record

ArticleThe Journal of experimental medicine2008

iPLA2beta: front and center in human monocyte chemotaxis to MCP-1.

Ravi S Mishra, Kevin A Carnevale, Martha K Cathcart

Open access · greenAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

41 citing papers in PubMed, 78 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. The cell biology of ferroptosis.Nature reviews. Molecular cell biology · 2024
    Review
  5. Review
  6. Article
  7. The Impact of the CaBiomolecules · 2021
    Review
  8. The Roles of Phospholipase AFrontiers in cell and developmental biology · 2021
    Review
  9. Article
  10. Article
  11. The roles of autotaxin/lysophosphatidic acid in immune regulation and asthma.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2020
    Review
  12. Macrophage polarization is linked to CaJournal of lipid research · 2020
    Article
  13. iPLABiochimica et biophysica acta. Molecular and cell biology of lipids · 2019
    Review
  14. Article
  15. Review
  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 2 institutions in 1 country.

Ravi S MishraDepartment of Cell Biology, Cleveland Clinic, Cleveland, OH 44195, USA.
Kevin A Carnevale
Martha K Cathcart
Cleveland Clinic · USUniversity of South Carolina · US

Funding

VIRALLY-INDUCED STAT-1, STAT-3 AND STAT-6M01RR018390 · NCRR · CLEVELAND CLINIC LERNER COM-CWRU · PI CULVER, DANIEL A · 2003 to 2007
$11.0M
MONOCYTE PATHOGENESIS--RESPIRATORY BURST OXIDASER01HL061971 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI CATHCART, MARTHA K · 1999 to 2007
$2.1M
NCRR NIH HHS M01 RR018390NCRR NIH HHS M01-RR-018390NHLBI NIH HHS HL 510681NHLBI NIH HHS HL 61971NHLBI NIH HHS R01 HL061971
6 · The paper itself

Abstract

Monocyte chemoattractant protein-1 (MCP-1) directs migration of blood monocytes to inflamed tissues. Despite the central role of chemotaxis in immune responses, the regulation of chemotaxis by signal transduction pathways and their in vivo significance remain to be thoroughly deciphered. In this study, we examined the intracellular location and functions of two recently identified regulators of chemotaxis, Ca(2+)-independent phospholipase (iPLA(2)beta) and cytosolic phospholipase (cPLA(2)alpha), and substantiate their in vivo importance. These enzymes are cytoplasmic in unstimulated monocytes. Upon MCP-1 stimulation, iPLA(2)beta is recruited to the membrane-enriched pseudopod. In contrast, cPLA(2)alpha is recruited to the endoplasmic reticulum. Although iPLA(2)beta or cPLA(2)alpha antisense oligodeoxyribonucleotide (ODN)-treated monocytes display reduced speed, iPLA(2)beta also regulates directionality and actin polymerization. iPLA(2)beta or cPLA(2)alpha antisense ODN-treated adoptively transferred mouse monocytes display a profound defect in migration to the peritoneum in vivo. These converging observations reveal that iPLA(2)beta and cPLA(2)alpha regulate monocyte migration from different intracellular locations, with iPLA(2)beta acting as a critical regulator of the cellular compass, and identify them as potential targets for antiinflammatory strategies.

Indexed as

ActinsAdoptive TransferAnimalsArachidonic AcidsCells, CulturedChemokine CCL2ChemotaxisFemaleGroup IV Phospholipases A2Group VI Phospholipases A2HumansLeukocytes, MononuclearMiceMice, Inbred BALB CMonocytesNaphthalenes6-(bromomethylene)tetrahydro-3-(1-naphthaleneyl)-2H-pyran-2-oneActinsArachidonic AcidsarachidonyltrifluoromethaneCCL2 protein, humanChemokine CCL2Group IV Phospholipases A2Group VI Phospholipases A2NaphthalenesOligodeoxyribonucleotides, AntisensePLA2G6 protein, humanPyrones

Identifiers

PMID18208975
PMCPMC2271028
OpenAlexW2162352961

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.