Evidence map›Paper›PMID 37415307›Full record

ArticleJournal of cellular and molecular medicine2023

Over-expression of Dyrk1A affects bleeding by modulating plasma fibronectin and fibrinogen level in mice.

Guillaume Postic, Jean Solarz, Cécile Loubière, Janany Kandiah, Jaysen Sawmynaden, Frederic Adam, Marie Vilaire, Thibaut Léger, Jean-Michel Camadro, Daniella Balduino Victorino and 6 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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

16 authors at 3 institutions in 1 country.

Guillaume PosticUniversité Paris Cité, BFA, UMR 8251, CNRS, ERLU1133, Paris, France.
Jean SolarzHITh, UMR_S1176, Institut National de la Santé et de la Recherche Médicale, Université Paris-Saclay, le Kremlin-Bicêtre, France.
Cécile LoubièreHITh, UMR_S1176, Institut National de la Santé et de la Recherche Médicale, Université Paris-Saclay, le Kremlin-Bicêtre, France.
Janany KandiahUniversité Paris Cité, BFA, UMR 8251, CNRS, Paris, France.
Jaysen SawmynadenUniversité Paris Cité, BFA, UMR 8251, CNRS, Paris, France.
Frederic AdamHITh, UMR_S1176, Institut National de la Santé et de la Recherche Médicale, Université Paris-Saclay, le Kremlin-Bicêtre, France.
Marie VilaireInstitut Médical Jérôme Lejeune, Paris, France.
Thibaut LégerUniversité Paris Cité, IJM, UMR 7592, CNRS, Paris, France.ORCID 0000-0002-6304-3433
Jean-Michel CamadroUniversité Paris Cité, IJM, UMR 7592, CNRS, Paris, France.
Daniella Balduino VictorinoICM Paris Brain Institute, CNRS UMR7225, INSERM U1127, Sorbonne University, Hôpital de la Pitié-Salpêtrière, Paris, France.
Marie-Claude PotierICM Paris Brain Institute, CNRS UMR7225, INSERM U1127, Sorbonne University, Hôpital de la Pitié-Salpêtrière, Paris, France.
Eric BunHITh, UMR_S1176, Institut National de la Santé et de la Recherche Médicale, Université Paris-Saclay, le Kremlin-Bicêtre, France.
Gautier MoroyUniversité Paris Cité, BFA, UMR 8251, CNRS, ERLU1133, Paris, France.
Alexandre KauskotHITh, UMR_S1176, Institut National de la Santé et de la Recherche Médicale, Université Paris-Saclay, le Kremlin-Bicêtre, France.
Olivier ChristopheHITh, UMR_S1176, Institut National de la Santé et de la Recherche Médicale, Université Paris-Saclay, le Kremlin-Bicêtre, France.
Nathalie JanelUniversité Paris Cité, BFA, UMR 8251, CNRS, Paris, France.ORCID 0000-0002-4746-8941
Centre National de la Recherche Scientifique · FRInserm · FRFondation Jérôme-Lejeune · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Down syndrome is the most common chromosomal abnormality in humans. Patients with Down syndrome have hematologic disorders, including mild to moderate thrombocytopenia. In case of Down syndrome, thrombocytopenia is not associated with bleeding, and it remains poorly characterized regarding molecular mechanisms. We investigated the effects of overexpression of Dyrk1A, an important factor contributing to some major Down syndrome phenotypes, on platelet number and bleeding in mice. Mice overexpressing Dyrk1A have a decrease in platelet number by 20%. However, bleeding time was found to be reduced by 50%. The thrombocytopenia and the decreased bleeding time observed were not associated to an abnormal platelet receptors expression, to a defect of platelet activation by ADP, thrombin or convulxin, to the presence of activated platelets in the circulation or to an abnormal half-life of the platelets. To propose molecular mechanisms explaining this discrepancy, we performed a network analysis of Dyrk1A interactome and demonstrated that Dyrk1A, fibronectin and fibrinogen interact indirectly through two distinct clusters of proteins. Moreover, in mice overexpressing Dyrk1A, increased plasma fibronectin and fibrinogen levels were found, linked to an increase of the hepatic fibrinogen production. Our results indicate that overexpression of Dyrk1A in mice induces decreased bleeding consistent with increased plasma fibronectin and fibrinogen levels, revealing a new role of Dyrk1A depending on its indirect interaction with these two proteins.

Indexed as

Down SyndromeThrombocytopeniaAnimalsBlood PlateletsDyrk KinasesFibrinogenFibronectinsHemorrhageHumansMiceDyrk KinasesFibrinogenFibronectinsbleeding timeDyrk1Afibrinogenfibronectinfilamin amiceplatelet

Identifiers

PMID37415307
PMCPMC10399536
OpenAlexW4383482420

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.