Evidence map›Paper›PMID 27081176›Full record

ArticleHaematologica2016

Human thrombopoiesis depends on Protein kinase Cδ/protein kinase Cε functional couple.

Cecilia Carubbi, Elena Masselli, Silvia Martini, Daniela Galli, Franco Aversa, Prisco Mirandola, Joseph E Italiano, Giuliana Gobbi, Marco Vitale

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
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  6. ROS in Platelet Biology: Functional Aspects and Methodological Insights.International journal of molecular sciences · 2020
    Review
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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

9 authors at 1 institution in 1 country.

Cecilia CarubbiDepartment of Biomedical, Biotechnological and Translational Sciences (SBiBiT), University of Parma, Italy.
Elena MasselliDepartment of Biomedical, Biotechnological and Translational Sciences (SBiBiT), University of Parma, Italy.
Silvia MartiniDepartment of Biomedical, Biotechnological and Translational Sciences (SBiBiT), University of Parma, Italy.
Daniela GalliDepartment of Biomedical, Biotechnological and Translational Sciences (SBiBiT), University of Parma, Italy.
Franco AversaDepartment of Clinical and Experimental Medicine, University of Parma, Italy.
Prisco MirandolaDepartment of Biomedical, Biotechnological and Translational Sciences (SBiBiT), University of Parma, Italy.
Joseph E ItalianoHematology Division, Department of Medicine, Brigham and Women's Hospital, and Harvard Medical School, Boston, MA, USA.
Giuliana GobbiDepartment of Biomedical, Biotechnological and Translational Sciences (SBiBiT), University of Parma, Italy.
Marco VitaleDepartment of Biomedical, Biotechnological and Translational Sciences (SBiBiT), University of Parma, Italy marco.vitale@unipr.it.
University of Parma · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A deeper understanding of the molecular events driving megakaryocytopoiesis and thrombopoiesis is essential to regulate in vitro and in vivo platelet production for clinical applications. We previously documented the crucial role of PKCε in the regulation of human and mouse megakaryocyte maturation and platelet release. However, since several data show that different PKC isoforms fulfill complementary functions, we targeted PKCε and PKCδ, which show functional and phenotypical reciprocity, at the same time as boosting platelet production in vitro. Results show that PKCδ, contrary to PKCε, is persistently expressed during megakaryocytic differentiation, and a forced PKCδ down-modulation impairs megakaryocyte maturation and platelet production. PKCδ and PKCε work as a functional couple with opposite roles on thrombopoiesis, and the modulation of their balance strongly impacts platelet production. Indeed, we show an imbalance of PKCδ/PKCε ratio both in primary myelofibrosis and essential thrombocythemia, featured by impaired megakaryocyte differentiation and increased platelet production, respectively. Finally, we demonstrate that concurrent molecular targeting of both PKCδ and PKCε represents a strategy for in vitro platelet factories.

Indexed as

ThrombopoiesisAdultAgedbcl-2-Associated X Proteinbcl-X ProteinBlood PlateletsCell DifferentiationFemaleGene ExpressionGene Expression RegulationHumansMaleMegakaryocytesMiddle AgedPrimary MyelofibrosisProtein Bindingbcl-2-Associated X Proteinbcl-X ProteinProtein Kinase C-deltaProtein Kinase C-epsilon

Identifiers

PMID27081176
PMCPMC5004460
OpenAlexW2339101325

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.