Evidence map›Paper›PMID 27599296›Full record

ArticleThe Journal of clinical investigation2016

A DOCK8-WIP-WASp complex links T cell receptors to the actin cytoskeleton.

Erin Janssen, Mira Tohme, Mona Hedayat, Marion Leick, Sudha Kumari, Narayanaswamy Ramesh, Michel J Massaad, Sumana Ullas, Veronica Azcutia, Christopher C Goodnow and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
8.7field-weighted citation impact, top 2% 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

73 citing papers in PubMed, 113 citations in OpenAlex.

  1. Article
  2. Article
  3. DOCK8 in immune cells: roles and mechanisms.Frontiers in immunology · 2026
    Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. CDC42 Regulatory Patterns Related To Inflammatory Bowel Disease and Hyperglycemia.Journal of bioinformatics and systems biology : Open access · 2025
    Article
  12. Article
  13. TThe Journal of allergy and clinical immunology · 2024
    Review
  14. Article
  15. WASP facilitates tumor mechanosensitivity in T lymphocytes.bioRxiv : the preprint server for biology · 2023
    Article
  16. Article
  17. Dendritic cells in inborn errors of immunity.Frontiers in immunology · 2023
    Review
  18. Article
  19. Article
  20. Article

13 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

19 authors at 4 institutions in 2 countries.

Erin Janssen
Mira Tohme
Mona Hedayat
Marion Leick
Sudha Kumari
Narayanaswamy Ramesh
Michel J Massaad
Sumana Ullas
Veronica Azcutia
Christopher C Goodnow
Katrina L Randall
Qi Qiao
Hao Wu
Waleed Al-Herz
Dianne Cox
John Hartwig
Darrell J Irvine
Francis W Luscinskas
Raif S Geha
Boston Children's Hospital · USHarvard University · USAustralian National University · AUAlbert Einstein College of Medicine · US

Funding

Role of DOCK8 in B Cell FunctionR01AI100315 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI GEHA, RAIF SALIM · 2013 to 2017
$2.2M
The role of DOCK8 in autoimmunityK08AI114968 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI JANSSEN, ERIN MARGARET · 2015 to 2019
$942k
NIAID NIH HHS K08 AI114968NIAID NIH HHS R01 AI100315
6 · The paper itself

Abstract

Wiskott-Aldrich syndrome (WAS) is associated with mutations in the WAS protein (WASp), which plays a critical role in the initiation of T cell receptor-driven (TCR-driven) actin polymerization. The clinical phenotype of WAS includes susceptibility to infection, allergy, autoimmunity, and malignancy and overlaps with the symptoms of dedicator of cytokinesis 8 (DOCK8) deficiency, suggesting that the 2 syndromes share common pathogenic mechanisms. Here, we demonstrated that the WASp-interacting protein (WIP) bridges DOCK8 to WASp and actin in T cells. We determined that the guanine nucleotide exchange factor activity of DOCK8 is essential for the integrity of the subcortical actin cytoskeleton as well as for TCR-driven WASp activation, F-actin assembly, immune synapse formation, actin foci formation, mechanotransduction, T cell transendothelial migration, and homing to lymph nodes, all of which also depend on WASp. These results indicate that DOCK8 and WASp are in the same signaling pathway that links TCRs to the actin cytoskeleton in TCR-driven actin assembly. Further, they provide an explanation for similarities in the clinical phenotypes of WAS and DOCK8 deficiency.

Indexed as

Actin CytoskeletonAdaptor Proteins, Signal TransducingAnimalsCarrier ProteinsCell MovementCytoskeletal ProteinsGuanine Nucleotide Exchange FactorsHEK293 CellsHumansImmunological SynapsesLymph NodesMechanotransduction, CellularMice, Inbred C57BLMice, KnockoutProtein BindingProtein Interaction MapsAdaptor Proteins, Signal TransducingCarrier ProteinsCytoskeletal ProteinsDock8 protein, mouseGuanine Nucleotide Exchange FactorsNEDD9 protein, mouseReceptors, Antigen, T-CellWaspip protein, mouseWiskott-Aldrich Syndrome Protein

Identifiers

PMID27599296
PMCPMC5096816
OpenAlexW2514175262

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.