Evidence map›Paper›PMID 32210425›Full record

ArticlePloS one2020

CD20 is dispensable for B-cell receptor signaling but is required for proper actin polymerization, adhesion and migration of malignant B cells.

Veronika Kozlova, Aneta Ledererova, Adriana Ladungova, Helena Peschelova, Pavlina Janovska, Aleksander Slusarczyk, Joanna Domagala, Pavel Kopcil, Viera Vakulova, Jan Oppelt and 5 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

15 citing papers in PubMed, 24 citations in OpenAlex.

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  14. Article
  15. Current State of CAR T-Cell Therapy in Chronic Lymphocytic Leukemia.International journal of molecular sciences · 2021
    Review
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

15 authors at 3 institutions in 2 countries.

Veronika KozlovaCentral European Institute of Technology (CEITEC), Masaryk University, Brno, Czech Republic.
Aneta LedererovaCentral European Institute of Technology (CEITEC), Masaryk University, Brno, Czech Republic.
Adriana LadungovaCentral European Institute of Technology (CEITEC), Masaryk University, Brno, Czech Republic.
Helena PeschelovaCentral European Institute of Technology (CEITEC), Masaryk University, Brno, Czech Republic.
Pavlina JanovskaDepartment of Experimental Biology, Faculty of Science, Masaryk University, Brno, Czech Republic.
Aleksander SlusarczykDepartment of Immunology, Medical University of Warsaw, Warsaw, Poland.
Joanna DomagalaDepartment of Immunology, Medical University of Warsaw, Warsaw, Poland.
Pavel KopcilCentral European Institute of Technology (CEITEC), Masaryk University, Brno, Czech Republic.
Viera VakulovaCentral European Institute of Technology (CEITEC), Masaryk University, Brno, Czech Republic.
Jan OppeltCentral European Institute of Technology (CEITEC), Masaryk University, Brno, Czech Republic.ORCID 0000-0002-3076-4840
Vitezslav BryjaDepartment of Experimental Biology, Faculty of Science, Masaryk University, Brno, Czech Republic.
Michael DoubekCentral European Institute of Technology (CEITEC), Masaryk University, Brno, Czech Republic.
Jiri MayerCentral European Institute of Technology (CEITEC), Masaryk University, Brno, Czech Republic.
Sarka PospisilovaCentral European Institute of Technology (CEITEC), Masaryk University, Brno, Czech Republic.
Michal SmidaCentral European Institute of Technology (CEITEC), Masaryk University, Brno, Czech Republic.ORCID 0000-0002-7335-3435
Central European Institute of Technology · CZMasaryk University · CZMedical University of Warsaw · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Surface protein CD20 serves as the critical target of immunotherapy in various B-cell malignancies for decades, however its biological function and regulation remain largely elusive. Better understanding of CD20 function may help to design improved rational therapies to prevent development of resistance. Using CRISPR/Cas9 technique, we have abrogated CD20 expression in five different malignant B-cell lines. We show that CD20 deletion has no effect upon B-cell receptor signaling or calcium flux. Also B-cell survival and proliferation is unaffected in the absence of CD20. On the contrary, we found a strong defect in actin cytoskeleton polymerization and, consequently, defective cell adhesion and migration in response to homeostatic chemokines SDF1α, CCL19 and CCL21. Mechanistically, we could identify a reduction in chemokine-triggered PYK2 activation, a calcium-activated signaling protein involved in activation of MAP kinases and cytoskeleton regulation. These cellular defects in consequence result in a severely disturbed homing of B cells in vivo.

Indexed as

ActinsAnimalsAntigens, CD20B-LymphocytesCell AdhesionCell Line, TumorCell MovementGene Knockdown TechniquesHumansLeukemia, B-CellLymphoma, B-CellMiceMice, Inbred NODMice, SCIDMice, TransgenicPolymerizationActinsAntigens, CD20Receptors, Antigen, B-Cell

Identifiers

PMID32210425
PMCPMC7094844
OpenAlexW3013608837

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.