Evidence map›Paper›PMID 33478008›Full record

ArticleInternational journal of molecular sciences2021

Mechanical Stress Induces Ca

Francesca Aglialoro, Asena Abay, Nurcan Yagci, Minke A E Rab, Lars Kaestner, Richard van Wijk, Marieke von Lindern, Emile van den Akker

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  4. Review
  5. Article
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  8. Article
  9. Piezo channels in the urinary system.Experimental & molecular medicine · 2022
    Review
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  11. Article
  12. 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

8 authors at 3 institutions in 2 countries.

Francesca AglialoroDepartment of Hematopoiesis, Sanquin Research and Landsteiner Laboratory, Amsterdam UMC, University of Amsterdam, 1012 WX Amsterdam, The Netherlands.
Asena AbayDepartment of Hematopoiesis, Sanquin Research and Landsteiner Laboratory, Amsterdam UMC, University of Amsterdam, 1012 WX Amsterdam, The Netherlands.
Nurcan YagciDepartment of Hematopoiesis, Sanquin Research and Landsteiner Laboratory, Amsterdam UMC, University of Amsterdam, 1012 WX Amsterdam, The Netherlands.
Minke A E RabDepartment of Clinical Chemistry and Haematology, University Medical Center Utrecht, 3584 CX Utrecht, The Netherlands.
Lars KaestnerDynamics of Fluids, Experimental Physics, Saarland University, 66123 Saarbrücken, Germany.
Richard van WijkDepartment of Clinical Chemistry and Haematology, University Medical Center Utrecht, 3584 CX Utrecht, The Netherlands.
Marieke von LindernDepartment of Hematopoiesis, Sanquin Research and Landsteiner Laboratory, Amsterdam UMC, University of Amsterdam, 1012 WX Amsterdam, The Netherlands.ORCID 0000-0001-6162-6320
Emile van den AkkerDepartment of Hematopoiesis, Sanquin Research and Landsteiner Laboratory, Amsterdam UMC, University of Amsterdam, 1012 WX Amsterdam, The Netherlands.
Sanquin · NLUniversity Medical Center Utrecht · NLSaarland University · DE

Funding

- RELEVANCE - H2020-MSCA-ITN-2015/H2020-MSCA-ITN-2015. 675115
6 · The paper itself

Abstract

Bioreactors are increasingly implemented for large scale cultures of various mammalian cells, which requires optimization of culture conditions. Such upscaling is also required to produce red blood cells (RBC) for transfusion and therapy purposes. However, the physiological suitability of RBC cultures to be transferred to stirred bioreactors is not well understood. PIEZO1 is the most abundantly expressed known mechanosensor on erythroid cells. It is a cation channel that translates mechanical forces directly into a physiological response. We investigated signaling cascades downstream of PIEZO1 activated upon transitioning stationary cultures to orbital shaking associated with mechanical stress, and compared the results to direct activation of PIEZO1 by the chemical agonist Yoda1. Erythroblasts subjected to orbital shaking displayed decreased proliferation, comparable to incubation in the presence of a low dose of Yoda1. Epo (Erythropoietin)-dependent STAT5 phosphorylation, and Calcineurin-dependent NFAT dephosphorylation was enhanced. Phosphorylation of ERK was also induced by both orbital shaking and Yoda1 treatment. Activation of these pathways was inhibited by intracellular Ca

Indexed as

Stress, MechanicalCalciumCalcium SignalingCell Culture TechniquesCell ProliferationCells, CulturedErythroblastsErythropoiesisHumansIon ChannelsMechanotransduction, CellularPyrazinesRotationThiadiazolesCalciumIon ChannelsPIEZO1 protein, humanPyrazinesThiadiazolesyoda-1calcium signal transductionmechanical stressPIEZO1

Identifiers

PMID33478008
PMCPMC7835781
OpenAlexW3124596089

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.