Evidence map›Paper›PMID 35428815›Full record

ArticleScientific reports2022

Megakaryocytes form linear podosomes devoid of digestive properties to remodel medullar matrix.

Antoine Oprescu, Déborah Michel, Adrien Antkowiak, Elodie Vega, Julien Viaud, Sara A Courtneidge, Anita Eckly, Henri de la Salle, Gaëtan Chicanne, Catherine Léon and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

3 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Inside-to-outside and back to the future of megakaryopoiesis.Research and practice in thrombosis and haemostasis · 2023
    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

12 authors at 7 institutions in 2 countries.

Antoine OprescuINSERM, UMR1297, Université Toulouse III, Institut des Maladies Métaboliques et Cardiovasculaires, Toulouse, France.
Déborah MichelINSERM, UMR1297, Université Toulouse III, Institut des Maladies Métaboliques et Cardiovasculaires, Toulouse, France.
Adrien AntkowiakINSERM, UMR1297, Université Toulouse III, Institut des Maladies Métaboliques et Cardiovasculaires, Toulouse, France.
Elodie VegaINSERM, UMR1297, Université Toulouse III, Institut des Maladies Métaboliques et Cardiovasculaires, Toulouse, France.
Julien ViaudINSERM, UMR1297, Université Toulouse III, Institut des Maladies Métaboliques et Cardiovasculaires, Toulouse, France.
Sara A CourtneidgeDepartment of Cell, Development and Cancer Biology, Oregon Health & Science University, Oregon, USA.
Anita EcklyINSERM, UMR_S1255, Université de Strasbourg, Etablissement Français du Sang-GEST, Strasbourg, France.
Henri de la SalleINSERM, UMR_S1255, Université de Strasbourg, Etablissement Français du Sang-GEST, Strasbourg, France.
Gaëtan ChicanneINSERM, UMR1297, Université Toulouse III, Institut des Maladies Métaboliques et Cardiovasculaires, Toulouse, France.
Catherine LéonINSERM, UMR_S1255, Université de Strasbourg, Etablissement Français du Sang-GEST, Strasbourg, France.
Bernard PayrastreINSERM, UMR1297, Université Toulouse III, Institut des Maladies Métaboliques et Cardiovasculaires, Toulouse, France.
Frédérique Gaits-IacovoniINSERM, UMR1297, Université Toulouse III, Institut des Maladies Métaboliques et Cardiovasculaires, Toulouse, France. frgaits@gmail.com.
Institut des Maladies Métaboliques et Cardiovasculaires · FRUniversité Toulouse III - Paul Sabatier · FRInserm · FRCentre Hospitalier Universitaire de Toulouse · FRÉtablissement Français du Sang · FROregon Health & Science University · USUniversité de Strasbourg · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone marrow megakaryocytes (MKs) undergo a maturation involving contacts with the microenvironment before extending proplatelets through sinusoids to deliver platelets in the bloodstream. We demonstrated that MKs assemble linear F-actin-enriched podosomes on collagen I fibers. Microscopy analysis evidenced an inverse correlation between the number of dot-like versus linear podosomes over time. Confocal videomicroscopy confirmed that they derived from each-other. This dynamics was dependent on myosin IIA. Importantly, MKs progenitors expressed the Tks4/5 adaptors, displayed a strong gelatinolytic ability and did not form linear podosomes. While maturing, MKs lost Tks expression together with digestive ability. However, those MKs were still able to remodel the matrix by exerting traction on collagen I fibers through a collaboration between GPVI, ß1 integrin and linear podosomes. Our data demonstrated that a change in structure and composition of podosomes accounted for the shift of function during megakaryopoiesis. These data highlight the fact that members of the invadosome family could correspond to different maturation status of the same entity, to adapt to functional responses required by differentiation stages of the cell that bears them.

Indexed as

MegakaryocytesPodosomesBlood PlateletsCollagen Type IThrombopoiesisCollagen Type I

Identifiers

PMID35428815
PMCPMC9012751
OpenAlexW4223902903

What OpenQuestion holds

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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.