Evidence map›Paper›PMID 31531757›Full record

ArticleMolecular and cellular biochemistry2020

Salivary extracellular vesicles can modulate purinergic signalling in oral tissues by combined ectonucleoside triphosphate diphosphohydrolases and ecto-5'-nucleotidase activities.

Débora A González, Martín M Barbieri van Haaster, Emmanuel Quinteros Villarruel, Claude Hattab, Mariano A Ostuni, Betina Orman

Abstract read
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In one paragraph

Article in Molecular and cellular biochemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Purinergic Signaling in Oral Tissues.International journal of molecular sciences · 2022
    Review
  5. Review
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

6 authors at 2 institutions in 2 countries.

Débora A GonzálezCátedra de Biofísica y Bioestadística, Facultad de Odontología, Universidad de Buenos Aires, M. T. de Alvear 2142, 1122, Buenos Aires, Argentina. debora.gonzalez@odontologia.uba.ar.ORCID http://orcid.org/0000-0002-9111-3427
Martín M Barbieri van HaasterCátedra de Biofísica y Bioestadística, Facultad de Odontología, Universidad de Buenos Aires, M. T. de Alvear 2142, 1122, Buenos Aires, Argentina.
Emmanuel Quinteros VillarruelCátedra de Farmacología, Facultad de Odontología, Universidad de Buenos Aires, M. T. de Alvear 2142, 1122, Buenos Aires, Argentina.
Claude HattabUniversité de Paris, Integrated Biology of Red Blood Cell UMR_S1134, INSERM, 75015, Paris, France.
Mariano A OstuniUniversité de Paris, Integrated Biology of Red Blood Cell UMR_S1134, INSERM, 75015, Paris, France.
Betina OrmanCátedra de Farmacología, Facultad de Odontología, Universidad de Buenos Aires, M. T. de Alvear 2142, 1122, Buenos Aires, Argentina.ORCID http://orcid.org/0000-0002-4584-4739
Universidad de Buenos Aires · ARInserm · FR

Funding

Universidad de Buenos Aires 2002015020012BAUniversidad de Buenos Aires 20720150100006BA
6 · The paper itself

Abstract

We reported previously that the rat submandibular gland is able to release nanovesicles capable to hydrolyse millimolar concentrations of ATP, ADP and AMP in vitro. Here, we show that rat saliva also contains nanovesicles with the ability to hydrolyse ATP. Our aim was to identify and characterize vesicular nucleotidases by using kinetic, immunological and in silico approaches. Nucleotidase activity in the absence or presence of specific inhibitors allowed us to assume the participation of NTPDase1, -2 and -3, together with ecto-5'-nucleotidase, confirmed using specific antibodies. At neutral pH, initial ATPase activity would be mostly due to NTPDase2, which was thereafter inactivated, leaving NTPDase1 and NTPDase3 to hydrolyse ATP and ADP with an efficacy ATPase/ADPase around 2. Ecto-5'nucleotidase would be mainly responsible for AMP hydrolysis and adenosine accumulation. We proposed a kinetic model for NTPDase2 as a tool to isolate and analyse the turnover of this enzyme in the presence of different ATP concentrations, including those expected in extracellular media. Our study characterizes the ectonucleotidases carried by extracellular vesicles which contribute to modulate ATP and adenosine concentrations in the oral cavity, essential players in purinergic signalling.

Indexed as

Signal Transduction5'-NucleotidaseAdenosineAdenosine TriphosphateAnimalsExtracellular VesiclesMouthPyrophosphatasesRatsRats, WistarSalivaSalivary Proteins and Peptides5'-NucleotidaseAdenosineAdenosine TriphosphatePyrophosphatasesSalivary Proteins and PeptidesEctonucleotidasesExtracellular ATPExtracellular vesiclesNTPDase2 inactivationPurinergic signallingSalivaSub mandibular gland

Identifiers

PMID31531757
OpenAlexW2974738984

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.