Evidence map›Paper›PMID 20156974›Full record

ArticleThe Journal of experimental medicine2010

ADAM10 is essential for Notch2-dependent marginal zone B cell development and CD23 cleavage in vivo.

David R Gibb, Mohey El Shikh, Dae-Joong Kang, Warren J Rowe, Rania El Sayed, Joanna Cichy, Hideo Yagita, John G Tew, Peter J Dempsey, Howard C Crawford and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed
9.5field-weighted citation impact, top 1% 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

96 citing papers in PubMed, 149 citations in OpenAlex.

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  16. TAO-kinase 3 governs the terminal differentiation of NOTCH2-dependent splenic conventional dendritic cells.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  17. Article
  18. Article
  19. Article
  20. Notch Signaling in B Cell Immune Responses.Frontiers in immunology · 2020
    Review

36 more citing papers are in PubMed but not listed here.

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

11 authors at 5 institutions in 3 countries.

David R GibbDepartment of Microbiology and Immunology, Virginia Commonwealth University School of Medicine, Richmond, VA 23298, USA.
Mohey El Shikh
Dae-Joong Kang
Warren J Rowe
Rania El Sayed
Joanna Cichy
Hideo Yagita
John G Tew
Peter J Dempsey
Howard C Crawford
Daniel H Conrad
Virginia Commonwealth University · USJagiellonian University · PLJuntendo University · JPStony Brook University · USUniversity of Michigan–Ann Arbor · US

Funding

The Effect of Lyn Deficiency on Mast Cell Activation and Inflammatory Disease ProU19AI077435 · NIAID · VIRGINIA COMMONWEALTH UNIVERSITY · PI SCHWARTZ, LAWRENCE B. · 2008 to 2012
$7.7M
STRUCTURE/FUNCTION OF THE LYMPHOCYTE FCE RECEPTORR01AI018697 · NIAID · VIRGINIA COMMONWEALTH UNIVERSITY · PI MARTIN, REBECCA KELLEY · 1985 to 2018
$6.5M
VCU Neuroscience Center Core GrantP30NS047463 · NINDS · VIRGINIA COMMONWEALTH UNIVERSITY · PI POVLISHOCK, JOHN T · 2003 to 2013
$5.0M
ADAM17 in pancreatic cancer and pancreatitisR01CA159222 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CRAWFORD, HOWARD C. · 2011 to 2015
$1.9M
Endogenous Betacellulin Signaling in Beta-cell BiologyR01DK063363 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DEMPSEY, PETER J · 2002 to 2006
$1.9M
Pancreatic Tumor Progression in the Absence of ADAM-mediated alpha-secretase ActiR03CA129579 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI CRAWFORD, HOWARD C. · 2007 to 2008
$155k
NCI NIH HHS R01 CA159222NCI NIH HHS R03 CA129579NCI NIH HHS R03CA129579NIAID NIH HHS R01 AI018697NIAID NIH HHS R01AI18697NIAID NIH HHS U19 AI077435NIAID NIH HHS U19AI077435NIDDK NIH HHS DK63363NIDDK NIH HHS R01 DK063363NINDS NIH HHS 5P30NS047463NINDS NIH HHS P30 NS047463
6 · The paper itself

Abstract

The proteolytic activity of a disintegrin and metalloproteinase 10 (ADAM10) regulates cell-fate decisions in Drosophila and mouse embryos. However, in utero lethality of ADAM10(-/-) mice has prevented examination of ADAM10 cleavage events in lymphocytes. To investigate their role in B cell development, we generated B cell-specific ADAM10 knockout mice. Intriguingly, deletion of ADAM10 prevented development of the entire marginal zone B cell (MZB) lineage. Additionally, cleavage of the low affinity IgE receptor, CD23, was profoundly impaired, but subsequent experiments demonstrated that ADAM10 regulates CD23 cleavage and MZB development by independent mechanisms. Development of MZBs is dependent on Notch2 signaling, which requires proteolysis of the Notch2 receptor by a previously unidentified proteinase. Further experiments revealed that Notch2 signaling is severely impaired in ADAM10-null B cells. Thus, ADAM10 critically regulates MZB development by initiating Notch2 signaling. This study identifies ADAM10 as the in vivo CD23 sheddase and an important regulator of B cell development. Moreover, it has important implications for the treatment of numerous CD23- and Notch-mediated pathologies, ranging from allergy to cancer.

Indexed as

ADAM10 ProteinADAM ProteinsAmyloid Precursor Protein SecretasesAnimalsB-LymphocytesDNA, ComplementaryExonsGene AmplificationGene DeletionMacrophagesMembrane ProteinsMiceMice, KnockoutPolymerase Chain ReactionReceptor, Notch2Receptors, CCR1ADAM10 ProteinAdam10 protein, mouseADAM ProteinsAmyloid Precursor Protein SecretasesDNA, ComplementaryMembrane ProteinsNotch2 protein, mouseReceptor, Notch2Receptors, CCR1Receptors, IgERNA

Identifiers

PMID20156974
PMCPMC2839139
OpenAlexW2159110897

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.