Evidence map›Paper›PMID 21880721›Full record

ArticleThe Journal of biological chemistry2011

Analysis of two major intracellular phospholipases A(2) (PLA(2)) in mast cells reveals crucial contribution of cytosolic PLA(2)α, not Ca(2+)-independent PLA(2)β, to lipid mobilization in proximal mast cells and distal fibroblasts.

Noriko Ueno, Yoshitaka Taketomi, Kei Yamamoto, Tetsuya Hirabayashi, Daisuke Kamei, Yoshihiro Kita, Takao Shimizu, Koei Shinzawa, Yoshihide Tsujimoto, Kazutaka Ikeda and 2 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Regulatory Roles of Phospholipase AFrontiers in immunology · 2022
    Review
  6. The Impact of the CaBiomolecules · 2021
    Review
  7. Article
  8. Group IID, IIE, IIF and III secreted phospholipase ABiochimica et biophysica acta. Molecular and cell biology of lipids · 2019
    Review
  9. Prostaglandins in asthma and allergic diseases.Pharmacology & therapeutics · 2019
    Review
  10. Article
  11. Article
  12. The Roles of the Secreted Phospholipase AAdvances in immunology · 2016
    Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. 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 1 country.

Noriko UenoLipid Metabolism Project, Tokyo Metropolitan Institute of Medical Science, 2-1-6 Kamikitazawa, Setagaya-ku, Tokyo 256-8506, Japan.
Yoshitaka Taketomi
Kei Yamamoto
Tetsuya Hirabayashi
Daisuke Kamei
Yoshihiro Kita
Takao Shimizu
Koei Shinzawa
Yoshihide Tsujimoto
Kazutaka Ikeda
Ryo Taguchi
Makoto Murakami
Tokyo Metropolitan Institute of Medical Science · JPThe University of Tokyo · JPOsaka University · JPJapan Science and Technology Agency · JPKeio University · JPShowa University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mast cells release a variety of mediators, including arachidonic acid (AA) metabolites, to regulate allergy, inflammation, and host defense, and their differentiation and maturation within extravascular microenvironments depend on the stromal cytokine stem cell factor. Mouse mast cells express two major intracellular phospholipases A(2) (PLA(2)s), namely group IVA cytosolic PLA(2) (cPLA(2)α) and group VIA Ca(2+)-independent PLA(2) (iPLA(2)β), and the role of cPLA(2)α in eicosanoid synthesis by mast cells has been well documented. Lipidomic analyses of mouse bone marrow-derived mast cells (BMMCs) lacking cPLA(2)α (Pla2g4a(-/-)) or iPLA(2)β (Pla2g6(-/-)) revealed that phospholipids with AA were selectively hydrolyzed by cPLA(2)α, not by iPLA(2)β, during FcεRI-mediated activation and even during fibroblast-dependent maturation. Neither FcεRI-dependent effector functions nor maturation-driven phospholipid remodeling was impaired in Pla2g6(-/-) BMMCs. Although BMMCs did not produce prostaglandin E(2) (PGE(2)), the AA released by cPLA(2)α from BMMCs during maturation was converted to PGE(2) by microsomal PGE synthase-1 (mPGES-1) in cocultured fibroblasts, and accordingly, Pla2g4a(-/-) BMMCs promoted microenvironmental PGE(2) synthesis less efficiently than wild-type BMMCs both in vitro and in vivo. Mice deficient in mPGES-1 (Ptges(-/-)) had an augmented local anaphylactic response. These results suggest that cPLA(2)α in mast cells is functionally coupled, through the AA transfer mechanism, with stromal mPGES-1 to provide anti-anaphylactic PGE(2). Although iPLA(2)β is partially responsible for PGE(2) production by macrophages and dendritic cells, it is dispensable for mast cell maturation and function.

Indexed as

AnaphylaxisAnimalsArachidonic AcidBone Marrow CellsCells, CulturedCoculture TechniquesDinoprostoneFibroblastsGroup IV Phospholipases A2Group VI Phospholipases A2Intramolecular OxidoreductasesMast CellsMiceMice, KnockoutPhospholipidsProstaglandin-E SynthasesArachidonic AcidDinoprostoneGroup IV Phospholipases A2Group VI Phospholipases A2Intramolecular OxidoreductasesPhospholipidsPla2g6 protein, mouseProstaglandin-E SynthasesPtges protein, mouse

Identifiers

PMID21880721
PMCPMC3199472
OpenAlexW1605937053

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.