Evidence map›Paper›PMID 35371049›Full record

ArticleFrontiers in immunology2022

The Small GTPase RHOA Links SLP65 Activation to PTEN Function in Pre B Cells and Is Essential for the Generation and Survival of Normal and Malignant B Cells.

Anila Vadakumchery, Hemin Faraidun, Omar El Ayoubi, Issame Outaleb, Vera Schmid, Hend Abdelrasoul, Timm Amendt, Ahmad Khadour, Corinna Setz, Katharina Göhring and 12 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 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
0.5field-weighted citation impact, top 37% 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, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

22 authors at 4 institutions in 2 countries.

Anila VadakumcheryInstitute of Immunology, Ulm University Medical Center, Ulm, Germany.
Hemin FaraidunDepartment of Molecular Immunology, Faculty of Biology, Albert Ludwigs University of Freiburg, Freiburg, Germany.
Omar El AyoubiInstitute of Immunology, Ulm University Medical Center, Ulm, Germany.
Issame OutalebDepartment of Molecular Immunology, Faculty of Biology, Albert Ludwigs University of Freiburg, Freiburg, Germany.
Vera SchmidInstitute of Immunology, Ulm University Medical Center, Ulm, Germany.
Hend AbdelrasoulInstitute of Immunology, Ulm University Medical Center, Ulm, Germany.
Timm AmendtInstitute of Immunology, Ulm University Medical Center, Ulm, Germany.
Ahmad KhadourInstitute of Immunology, Ulm University Medical Center, Ulm, Germany.
Corinna SetzInstitute of Immunology, Ulm University Medical Center, Ulm, Germany.
Katharina GöhringInstitute of Immunology, Ulm University Medical Center, Ulm, Germany.
Karoline LoddInstitute of Immunology, Ulm University Medical Center, Ulm, Germany.
Christoffer HitzingInstitute of Cellular & Molecular Immunology, University Medical Center Göttingen, Göttingen, Germany.
Alabbas AlkhatibDepartment of Molecular Immunology, Faculty of Biology, Albert Ludwigs University of Freiburg, Freiburg, Germany.
Mayas BilalInstitute of Immunology, Ulm University Medical Center, Ulm, Germany.
Julian BenckendorffInstitute of Pathology, Ulm University Medical Center, Ulm, Germany.
Abdul Kader Al ShugriInstitute of Pathology, Ulm University Medical Center, Ulm, Germany.
Cord Herbert BrakebuschBiotech Research and Innovation Center (BRIC), University of Copenhagen, Copenhagen, Denmark.
Niklas EngelsInstitute of Cellular & Molecular Immunology, University Medical Center Göttingen, Göttingen, Germany.
Moumita DattaInstitute of Immunology, Ulm University Medical Center, Ulm, Germany.
Elias HobeikaInstitute of Immunology, Ulm University Medical Center, Ulm, Germany.
Ameera AlsadeqInstitute of Immunology, Ulm University Medical Center, Ulm, Germany.
Hassan JumaaInstitute of Immunology, Ulm University Medical Center, Ulm, Germany.
Universität Ulm · DEUniversity of Freiburg · DEUniversitätsmedizin Göttingen · DEUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The generation, differentiation, survival and activation of B cells are coordinated by signals emerging from the B cell antigen receptor (BCR) or its precursor, the pre-BCR. The adaptor protein SLP65 (also known as BLNK) is an important signaling factor that controls pre-B cell differentiation by down-regulation of PI3K signaling. Here, we investigated the mechanism by which SLP65 interferes with PI3K signaling. We found that SLP65 induces the activity of the small GTPase RHOA, which activates PTEN, a negative regulator of PI3K signaling, by enabling its translocation to the plasma membrane. The essential role of RHOA is confirmed by the complete block in early B cell development in conditional

Indexed as

Monomeric GTP-Binding ProteinsPrecursor Cells, B-LymphoidAdaptor Proteins, Signal TransducingAnimalsMicePhosphatidylinositol 3-KinasesReceptors, Antigen, B-CellrhoA GTP-Binding ProteinAdaptor Proteins, Signal TransducingMonomeric GTP-Binding ProteinsPhosphatidylinositol 3-KinasesReceptors, Antigen, B-CellrhoA GTP-Binding ProteinRhoA protein, mouseBCR-ABLCLLPI3K signalingPTENRHOASLP65

Identifiers

PMID35371049
PMCPMC8965026
OpenAlexW4220907305

What Socratic holds

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LicenceCC BY
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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.