Evidence map›Paper›PMID 24967784›Full record

ArticlePLoS genetics2014

Rasa3 controls megakaryocyte Rap1 activation, integrin signaling and differentiation into proplatelet.

Patricia Molina-Ortiz, Séléna Polizzi, Eve Ramery, Stéphanie Gayral, Céline Delierneux, Cécile Oury, Shintaro Iwashita, Stéphane Schurmans

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

21 citing papers in PubMed, 34 citations in OpenAlex.

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  20. RAP1-GTPase signaling and platelet function.Journal of molecular medicine (Berlin, Germany) · 2016
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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 at 3 institutions in 2 countries.

Patricia Molina-OrtizLaboratory of Functional Genetics, GIGA-Research Centre, Université de Liège, Liège, and Welbio, Belgium.
Séléna PolizziInstitut de Recherches Interdisciplinaires en Biologie Humaine et Moléculaire (IRIBHM), Institut de Biologie et de Médecine Moléculaires (IBMM), Faculté de Médecine, Université Libre de Bruxelles, Gosselies, Belgium.
Eve RameryLaboratoire de Biologie Clinique, Faculté de Médecine-vétérinaire, Université de Liège, Liège, Belgium.
Stéphanie GayralInstitut de Recherches Interdisciplinaires en Biologie Humaine et Moléculaire (IRIBHM), Institut de Biologie et de Médecine Moléculaires (IBMM), Faculté de Médecine, Université Libre de Bruxelles, Gosselies, Belgium.
Céline DelierneuxLaboratory of Thrombosis and Hemostasis, GIGA-Research Centre, Université de Liège, Liège, Belgium.
Cécile OuryLaboratory of Thrombosis and Hemostasis, GIGA-Research Centre, Université de Liège, Liège, Belgium.
Shintaro IwashitaMitsubishi Kagaku Institute of Life Sciences and Faculty of Pharmacy, Iwaki Meisei University, Iwaki, Japan.
Stéphane SchurmansLaboratory of Functional Genetics, GIGA-Research Centre, Université de Liège, Liège, and Welbio, Belgium; Institut de Recherches Interdisciplinaires en Biologie Humaine et Moléculaire (IRIBHM), Institut de Biologie et de Médecine Moléculaires (IBMM), Faculté de Médecine, Université Libre de Bruxelles, Gosselies, Belgium.
University of Liège · BEUniversité Libre de Bruxelles · BEIwaki Meisei University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rasa3 is a GTPase activating protein of the GAP1 family which targets Ras and Rap1. Ubiquitous Rasa3 catalytic inactivation in mouse results in early embryonic lethality. Here, we show that Rasa3 catalytic inactivation in mouse hematopoietic cells results in a lethal syndrome characterized by severe defects during megakaryopoiesis, thrombocytopenia and a predisposition to develop preleukemia. The main objective of this study was to define the cellular and the molecular mechanisms of terminal megakaryopoiesis alterations. We found that Rasa3 catalytic inactivation altered megakaryocyte development, adherence, migration, actin cytoskeleton organization and differentiation into proplatelet forming megakaryocytes. These megakaryocyte alterations were associated with an increased active Rap1 level and a constitutive integrin activation. Thus, these mice presented a severe thrombocytopenia, bleeding and anemia associated with an increased percentage of megakaryocytes in the bone marrow, bone marrow fibrosis, extramedular hematopoiesis, splenomegaly and premature death. Altogether, our results indicate that Rasa3 catalytic activity controls Rap1 activation and integrin signaling during megakaryocyte differentiation in mouse.

Indexed as

AnimalsBlood PlateletsBone Marrow CellsCell DifferentiationFemurFlow CytometryGTPase-Activating ProteinsHematopoiesisIntegrinsMegakaryocytesMiceShelterin ComplexSignal TransductionSpleenTelomere-Binding ProteinsGTPase-Activating ProteinsIntegrinsRASA3 protein, mouseShelterin ComplexTelomere-Binding ProteinsTERF2IP protein, mouse

Identifiers

PMID24967784
PMCPMC4072513
OpenAlexW2113698549

What OpenQuestion 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 OpenQuestion graph.