Evidence map›Paper›PMID 21971714›Full record

ArticleJournal of lipid research2011

Lipid body formation during maturation of human mast cells.

Andrea Dichlberger, Stefanie Schlager, Jani Lappalainen, Reijo Käkelä, Katarina Hattula, Sarah J Butcher, Wolfgang J Schneider, Petri T Kovanen

Registry-linked trialAbstract read
In one paragraph

Article in Journal of lipid research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02498119 (The Role of Arachidonic Acid Metabolites, in the Lipid Droplets of Macrophages From Patients With Metabolic Syndrome), which is not on this map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
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.

NCT02498119 unknown statusnot on this mapstarted 2014, after this paper: background citation

The Role of Arachidonic Acid Metabolites, in the Lipid Droplets of Macrophages From Patients With Metabolic Syndrome

Typeobservational_patient_registrySponsorUniversity of MalayaRan2014 to 2016Enrolled12ConditionsType 2 Diabetes Mellitus
3 · Its place in the literature

Who cites it

22 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Lipid droplet functions beyond energy storage.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2017
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  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

8 authors.

Andrea DichlbergerWihuri Research Institute, 00140 Helsinki, Finland.
Stefanie SchlagerWihuri Research Institute, 00140 Helsinki, Finland.
Jani LappalainenWihuri Research Institute, 00140 Helsinki, Finland.
Reijo KäkeläDepartment of Biosciences, FIN-00014 University of Helsinki, Finland and.
Katarina HattulaInstitute of Biotechnology, FIN-00014 University of Helsinki, Finland; and.
Sarah J ButcherInstitute of Biotechnology, FIN-00014 University of Helsinki, Finland; and.
Wolfgang J SchneiderDepartment of Medical Biochemistry, Medical University Vienna, 1030 Vienna, Austria. Electronic address: wolfgang.schneider@meduniwien.ac.at.
Petri T KovanenWihuri Research Institute, 00140 Helsinki, Finland. Electronic address: petri.kovanen@wri.fi.

Funding

Austrian Science Fund FWF J 2994
6 · The paper itself

Abstract

Lipid droplets, also called lipid bodies (LB) in inflammatory cells, are important cytoplasmic organelles. However, little is known about the molecular characteristics and functions of LBs in human mast cells (MC). Here, we have analyzed the genesis and components of LBs during differentiation of human peripheral blood-derived CD34(+) progenitors into connective tissue-type MCs. In our serum-free culture system, the maturing MCs, derived from 18 different donors, invariably developed triacylglycerol (TG)-rich LBs. Not known heretofore, the MCs transcribe the genes for perilipins (PLIN)1-4, but not PLIN5, and PLIN2 and PLIN3 display different degrees of LB association. Upon MC activation and ensuing degranulation, the LBs were not cosecreted with the cytoplasmic secretory granules. Exogenous arachidonic acid (AA) enhanced LB genesis in Triacsin C-sensitive fashion, and it was found to be preferentially incorporated into the TGs of LBs. The large TG-associated pool of AA in LBs likely is a major precursor for eicosanoid production by MCs. In summary, we demonstrate that cultured human MCs derived from CD34(+) progenitors in peripheral blood provide a new tool to study regulatory mechanisms involving LB functions, with particular emphasis on AA metabolism, eicosanoid biosynthesis, and subsequent release of proinflammatory lipid mediators from these cells.

Indexed as

Lipid MetabolismAntigens, CD34Arachidonic AcidsCell DegranulationCell DifferentiationCytoplasmGene Expression RegulationHumansLipidsMast CellsMembrane ProteinsPerilipin-2Perilipin-3Stem CellsTriglyceridesVesicular Transport ProteinsAntigens, CD34Arachidonic AcidsLipidsMembrane ProteinsPerilipin-2Perilipin-3PLIN2 protein, humanPLIN3 protein, humanTriglyceridesVesicular Transport Proteins

Identifiers

PMID21971714
PMCPMC3220288

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.