Evidence map›Paper›PMID 23962808›Full record

ArticleThe Journal of investigative dermatology2014

NKG2D triggers cytotoxicity in murine epidermal γδ T cells via PI3K-dependent, Syk/ZAP70-independent signaling pathway.

Atsuko Ibusuki, Kazuhiro Kawai, Shigeru Yoshida, Youhei Uchida, Ayano Nitahara-Takeuchi, Kimiko Kuroki, Mizuho Kajikawa, Toyoyuki Ose, Katsumi Maenaka, Masanori Kasahara and 1 more

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In one paragraph

Article in The Journal of investigative dermatology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

20 citing papers in PubMed, 29 citations in OpenAlex.

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  10. Epidermal resident γδ T cell development and function in skin.Cellular and molecular life sciences : CMLS · 2021
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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 1 country.

Atsuko IbusukiDepartment of Dermatology, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
Kazuhiro KawaiDepartment of Dermatology, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan; Department of Dermatology, Kido Hospital, Niigata, Japan. Electronic address: kazkawai@m2.kufm.kagoshima-u.ac.jp.
Shigeru YoshidaDepartment of Medical Laboratory Science, Faculty of Health Sciences, Hokkaido University, Sapporo, Japan; Department of Pathology, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
Youhei UchidaDepartment of Dermatology, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
Ayano Nitahara-TakeuchiDivision of Dermatology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Kimiko KurokiLaboratory of Biomolecular Science, Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan.
Mizuho KajikawaLaboratory for Infectious Immunity, Research Center for Allergy and Immunology (RCAI), RIKEN Yokohama Institute, Yokohama, Japan.
Toyoyuki OseLaboratory of Biomolecular Science, Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan.
Katsumi MaenakaLaboratory of Biomolecular Science, Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan.
Masanori KasaharaDepartment of Pathology, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
Takuro KanekuraDepartment of Dermatology, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
Hokkaido University · JPKagoshima University · JPNiigata University · JPRIKEN Center for Integrative Medical Sciences · JPSapporo Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Murine epidermal γδ T cells, known as dendritic epidermal T cells (DETCs), survey tissue stress through the invariant T-cell receptor (TCR) and non-clonotypic receptors such as NKG2D. NKG2D signaling via the DAP10-phosphatidylinositol 3-kinase (PI3K) pathway directly stimulates cytotoxicity in natural killer (NK) cells and costimulates CD8(+) T cells to augment TCR signals. In activated murine NK cells, NKG2D signals also via the DAP12-Syk/ZAP70 pathway that triggers both cytotoxicity and cytokine production. It remains controversial whether NKG2D on DETCs is a primary activating receptor or functions only as a costimulatory receptor, and signaling pathways initiated by NKG2D ligation in DETCs have not been analyzed. We show that stimulation of short-term DETC lines with recombinant NKG2D ligands triggers degranulation (exocytosis of cytotoxic granules) via the PI3K-dependent signaling pathway, but does not induce cytokine production or Syk/ZAP70 activation. Coengagement of TCR or Syk/ZAP70 signaling was not crucial for DETC-mediated killing of NKG2D ligand-expressing target cells. Thus, NKG2D can function as a coactivating stress receptor that directly triggers cytotoxicity in DETCs, at least after priming, via the PI3K-dependent, Syk/ZAP70-independent signaling pathway.

Indexed as

AnimalsAntibodies, MonoclonalCell LineCytoplasmic GranulesEpidermal CellsEpidermisExocytosisIntracellular Signaling Peptides and ProteinsKiller Cells, NaturalLangerhans CellsMiceMice, Inbred C57BLNK Cell Lectin-Like Receptor Subfamily KPhosphatidylinositol 3-KinasesProtein-Tyrosine KinasesReceptors, Antigen, T-Cell, gamma-deltaAntibodies, MonoclonalIntracellular Signaling Peptides and ProteinsKlrk1 protein, mouseNK Cell Lectin-Like Receptor Subfamily KPhosphatidylinositol 3-KinasesProtein-Tyrosine KinasesReceptors, Antigen, T-Cell, gamma-deltaSyk KinaseSyk protein, mouseZap70 protein, mouseZAP-70 Protein-Tyrosine Kinase

Identifiers

PMID23962808
OpenAlexW2057567013

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.