Evidence map›Paper›PMID 17213309›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2007

WIP is a chaperone for Wiskott-Aldrich syndrome protein (WASP).

Miguel A de la Fuente, Yoji Sasahara, Marco Calamito, Inés M Antón, Abdallah Elkhal, Maria D Gallego, Koduru Suresh, Katherine Siminovitch, Hans D Ochs, Kenneth C Anderson and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed, 1 pooled it
5.6field-weighted citation impact, top 3% 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

76 citing papers in PubMed, 1 synthesis or guideline pooled it, 165 citations in OpenAlex.

  1. Pooled it
  2. Review
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  7. Article
  8. Dendritic cells in inborn errors of immunity.Frontiers in immunology · 2023
    Review
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  14. Wiskott-Aldrich Syndrome Protein: Roles in Signal Transduction in T Cells.Frontiers in cell and developmental biology · 2021
    Review
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16 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

13 authors at 6 institutions in 3 countries.

Miguel A de la FuenteDivision of Immunology, Children's Hospital Boston, One Blackfan Circle, Boston, MA 02115, USA.
Yoji Sasahara
Marco Calamito
Inés M Antón
Abdallah Elkhal
Maria D Gallego
Koduru Suresh
Katherine Siminovitch
Hans D Ochs
Kenneth C Anderson
Fred S Rosen
Raif S Geha
Narayanaswamy Ramesh
Boston Children's Hospital · USHarvard University · USCentro de Biología Molecular Severo Ochoa · ESDana-Farber Cancer Institute · USMount Sinai Hospital · CAUniversity of Washington · US

Funding

WIP in TCR signaling and actin reorganizationP01HL059561 · NHLBI · IMMUNE DISEASE INSTITUTE, INC. · PI GEHA, RAIF SALIM · 1997 to 2012
$21.8M
TRANSGENIC MODELS OF T CELL RECEPTOR IMMUNODEFICIENCIESP01AI035714 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI TERHORST, CORNELIS P · 1994 to 2007
$9.3M
Primary Immunodeficiency Research ConsortiumN01AI30070 · NIAID · PRIMARY IMMUNODEFICIENCY RES CONSORTIUM · PI OCHS, HANS · 2007 to 2010
$7.2M
STAT3 Functional Defects and a Novel Therapeutic Approach for Hyper IgE SyndromeR37HD017427 · NICHD · UNIVERSITY OF WASHINGTON · PI OCHS, HANS D · 1999 to 2009
$3.1M
PRIMARY IMMUNODEFICIENCY DISEASE REGISTRY-266030070-266030070N01AI030070 · NIAID · PIRC, INC. · 2003 to 2005
–
DEVELOPMENTAL AND GENETIC DEFECTS OF IMMUNITYR01HD017427 · NICHD · UNIVERSITY OF WASHINGTON · PI OCHS, HANS D · 1985 to 1998
–
NHLBI NIH HHS HL 59561NHLBI NIH HHS P01 HL059561NIAID NIH HHS AI 35714NIAID NIH HHS N01 AI030070NIAID NIH HHS N01 AI 30070NIAID NIH HHS P01 AI035714NICHD NIH HHS HD 17427NICHD NIH HHS R37 HD017427
6 · The paper itself

Abstract

Wiskott-Aldrich syndrome protein (WASP) is in a complex with WASP-interacting protein (WIP). WASP levels, but not mRNA levels, were severely diminished in T cells from WIP(-/-) mice and were increased by introduction of WIP in these cells. The WASP binding domain of WIP was shown to protect WASP from degradation by calpain in vitro. Treatment with the proteasome inhibitors MG132 and bortezomib increased WASP levels in T cells from WIP(-/-) mice and in T and B lymphocytes from two WAS patients with missense mutations (R86H and T45M) that disrupt WIP binding. The calpain inhibitor calpeptin increased WASP levels in activated T and B cells from the WASP patients, but not in primary T cells from the patients or from WIP(-/-) mice. Despite its ability to increase WASP levels proteasome inhibition did not correct the impaired IL-2 gene expression and low F-actin content in T cells from the R86H WAS patient. These results demonstrate that WIP stabilizes WASP and suggest that it may also be important for its function.

Indexed as

ActinsAnimalsArginineBoronic AcidsBortezomibCalpainCarrier ProteinsCytoskeletal ProteinsEnzyme InhibitorsHumansInterleukin-2Intracellular Signaling Peptides and ProteinsJurkat CellsLymphocytesMiceMice, KnockoutActinsArginineBoronic AcidsBortezomibCalpainCarrier ProteinsCytoskeletal ProteinsEnzyme InhibitorsInterleukin-2Intracellular Signaling Peptides and ProteinsMolecular ChaperonesProteasome Endopeptidase ComplexProteasome InhibitorsPyrazinesWaspip protein, mouseWIPF1 protein, humanWiskott-Aldrich Syndrome Protein

Identifiers

PMID17213309
PMCPMC1783416
OpenAlexW1984259502

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.