Evidence map›Paper›PMID 26655718›Full record

ArticleThe Journal of biological chemistry2016

Progesterone-induced Acrosome Exocytosis Requires Sequential Involvement of Calcium-independent Phospholipase A2β (iPLA2β) and Group X Secreted Phospholipase A2 (sPLA2).

Roland Abi Nahed, Guillaume Martinez, Jessica Escoffier, Sandra Yassine, Thomas Karaouzène, Jean-Pascal Hograindleur, John Turk, George Kokotos, Pierre F Ray, Serge Bottari and 3 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Updating Phospholipase ABiomolecules · 2020
    Review
  7. Article
  8. Small-molecule inhibitors as potential therapeutics and as tools to understand the role of phospholipases ABiochimica et biophysica acta. Molecular and cell biology of lipids · 2019
    Review
  9. iPLABiochimica et biophysica acta. Molecular and cell biology of lipids · 2019
    Review
  10. β-Lactones: A Novel Class of CaJournal of medicinal chemistry · 2019
    Article
  11. Article
  12. Article
  13. Article
  14. Observational
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

13 authors at 6 institutions in 3 countries.

Roland Abi NahedFrom the Université Grenoble Alpes, F-38000 Grenoble, France, the Institut Albert Bonniot, INSERM U823, La Tronche F-38700, France.
Guillaume MartinezFrom the Université Grenoble Alpes, F-38000 Grenoble, France, the Institut Albert Bonniot, INSERM U823, La Tronche F-38700, France.
Jessica EscoffierFrom the Université Grenoble Alpes, F-38000 Grenoble, France, the Institut Albert Bonniot, INSERM U823, La Tronche F-38700, France.
Sandra YassineFrom the Université Grenoble Alpes, F-38000 Grenoble, France, the Institut Albert Bonniot, INSERM U823, La Tronche F-38700, France.
Thomas KaraouzèneFrom the Université Grenoble Alpes, F-38000 Grenoble, France, the Institut Albert Bonniot, INSERM U823, La Tronche F-38700, France.
Jean-Pascal HograindleurFrom the Université Grenoble Alpes, F-38000 Grenoble, France, the Institut Albert Bonniot, INSERM U823, La Tronche F-38700, France.
John Turkthe Division of Endocrinology, Metabolism and Lipid Research, Washington University School of Medicine, St. Louis, Missouri 63110.
George Kokotosthe Department of Chemistry, University of Athens, Panepistimiopolis, Athens 15771, Greece.
Pierre F RayFrom the Université Grenoble Alpes, F-38000 Grenoble, France, the Institut Albert Bonniot, INSERM U823, La Tronche F-38700, France, the Centre Hospitalier Universitaire de Grenoble, Unité Fonctionnelle de Biochimie et Génétique Moléculaire, Grenoble F-38000, France.
Serge BottariFrom the Université Grenoble Alpes, F-38000 Grenoble, France, the Institut Albert Bonniot, INSERM U823, La Tronche F-38700, France, the Centre Hospitalier Universitaire de Grenoble, Plate-forme de Radioanalyse, IBP, CS10217, Grenoble F-38000, France.
Gérard Lambeauthe Université de Nice-Sophia Antipolis, Valbonne 06560, France, the Centre Hospitalier Universitaire de Grenoble, Centre d'AMP-CECOS, CS1021, Grenoble F-38000, France.
Sylviane HennebicqFrom the Université Grenoble Alpes, F-38000 Grenoble, France, the Institut Albert Bonniot, INSERM U823, La Tronche F-38700, France, the Centre Hospitalier Universitaire de Grenoble, Centre d'AMP-CECOS, CS1021, Grenoble F-38000, France.
Christophe ArnoultFrom the Université Grenoble Alpes, F-38000 Grenoble, France, the Institut Albert Bonniot, INSERM U823, La Tronche F-38700, France, Christophe.arnoult@ujf-grenoble.fr.
Université Grenoble Alpes · FRInstitut pour l'avancée des biosciences · FRInserm · FRNational and Kapodistrian University of Athens · GRUniversité Côte d'Azur · FRWashington University in St. Louis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Phospholipase A2 (PLA2) activity has been shown to be involved in the sperm acrosome reaction (AR), but the molecular identity of PLA2 isoforms has remained elusive. Here, we have tested the role of two intracellular (iPLA2β and cytosolic PLA2α) and one secreted (group X) PLA2s in spontaneous and progesterone (P4)-induced AR by using a set of specific inhibitors and knock-out mice. iPLA2β is critical for spontaneous AR, whereas both iPLA2β and group X secreted PLA2 are involved in P4-induced AR. Cytosolic PLA2α is dispensable in both types of AR. P4-induced AR spreads over 30 min in the mouse, and kinetic analyses suggest the presence of different sperm subpopulations, using distinct PLA2 pathways to achieve AR. At low P4 concentration (2 μm), sperm undergoing early AR (0-5 min post-P4) rely on iPLA2β, whereas sperm undergoing late AR (20-30 min post-P4) rely on group X secreted PLA2. Moreover, the role of PLA2s in AR depends on P4 concentration, with the PLA2s being key actors at low physiological P4 concentrations (≤2 μm) but not at higher P4 concentrations (~10 μm).

Indexed as

AcrosomeAcrosome ReactionAnimalsExocytosisGroup VI Phospholipases A2Group X Phospholipases A2MaleMiceMice, KnockoutProgesteroneGroup VI Phospholipases A2Group X Phospholipases A2Pla2g6 protein, mouseProgesteroneacrosomeexocytosisiPLA2βphospholipase Aprogesteronesecreted PLA2spermspermatogenesis

Identifiers

PMID26655718
PMCPMC4742768
OpenAlexW2419163840

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.