Evidence map›Paper›PMID 31408613›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2019

CD82 controls CpG-dependent TLR9 signaling.

Nida S Khan, Daniel P Lukason, Marianela Feliu, Rebecca A Ward, Allison K Lord, Jennifer L Reedy, Zaida G Ramirez-Ortiz, Jenny M Tam, Pia V Kasperkovitz, Paige E Negoro and 15 more

Open access · hybridAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Toll-like receptors in cardiac hypertrophy.Frontiers in cardiovascular medicine · 2023
    Review
  9. Toll-like Receptor Mediation in SARS-CoV-2: A Therapeutic Approach.International journal of molecular sciences · 2022
    Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Tetraspanins in the regulation of mast cell function.Medical microbiology and immunology · 2020
    Review
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

25 authors at 13 institutions in 5 countries.

Nida S KhanDivision of Infectious Disease, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Daniel P LukasonDivision of Infectious Disease, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Marianela FeliuDivision of Infectious Disease, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Rebecca A WardDivision of Infectious Disease, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Allison K LordDivision of Infectious Disease, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Jennifer L ReedyDivision of Infectious Disease, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Zaida G Ramirez-OrtizDepartment of Medicine, Harvard Medical School, Boston, Massachusetts, USA.
Jenny M TamDivision of Infectious Disease, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Pia V KasperkovitzF. Hoffmann-La Roche Innovation Center Basel, Basel, Switzerland.
Paige E NegoroDivision of Infectious Disease, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Tammy D VyasDivision of Infectious Disease, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Shuying XuDivision of Infectious Disease, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Melanie M BrinkmannViral Immune Modulation Research Group, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Mridu AcharayaBenaroya Research Institute, Seattle, Washington, USA.
Katerina Artavanis-TsakonasDepartment of Pathology, University of Cambridge, Cambridge, United Kingdom.
Eva-Maria FrickelHost-Toxoplasma Interaction Laboratory, The Francis Crick Institute, London, United Kingdom.
Christine E BeckerCenter for Computational and Integrative Biology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Zeina DagherDivision of Infectious Disease, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
You-Me KimGerman Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.
Eicke LatzDepartment of Medicine, University of Massachusetts Medical School, Boston, Massachusetts, USA.
Hidde L PloeghBoston Children's Hospital, Boston, Massachusetts, USA.
Michael K MansourDivision of Infectious Disease, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Cindy K MirantiLaboratory of Integrin Signaling and Tumorigenesis, Van Andel Research Institute, Grand Rapids, Michigan, USA.
Stuart M LevitzDepartment of Medicine, University of Massachusetts Medical School, Boston, Massachusetts, USA.
Jatin M VyasDivision of Infectious Disease, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Massachusetts General Hospital · USBoston Children's Museum · USENT and Allergy · USHelmholtz Centre for Infection Research · DEKorea Advanced Institute of Science and Technology · KRRoche (Switzerland) · CHSeattle Children's Hospital · USThe Francis Crick Institute · GBUniversity of Arizona · USUniversity of Bonn · DEUniversity of Cambridge · GBUniversity of Massachusetts Boston · USUniversity of Massachusetts Lowell · US

Funding

ROLE OF MACROPHAGES IN CRYPTOCOCCAL INFECTIONSR01AI025780 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI LEVITZ, STUART MICHAEL · 1987 to 2019
$7.1M
The Functional Role of the Tetraspanin CD82/Kai1 in Fungal Innate ImmunityR01AI136529 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI VYAS, JATIN M · 2018 to 2022
$2.7M
Functional Role of the Tetraspanin CD82/Kai1 in Innate and Adaptive ImmunityR01AI092084 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI VYAS, JATIN M · 2011 to 2015
$2.2M
The contribution of eosinophils and the IL-23/IL-17 axis to host responses to AspergillusR01AI139615 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI LEVITZ, STUART MICHAEL · 2018 to 2021
$1.7M
The role of TLR9 on Aspergillus fumigatus phagosomesR01AI097519 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI VYAS, JATIN M · 2013 to 2016
$1.6M
The role of spleen tyrosine kinase (syk) in neutrophil responses to pathogenic fungi.R01AI132638 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI MANSOUR, MICHAEL K · 2018 to 2021
$1.6M
Cancer Research UK FC001076Medical Research Council FC001076Medical Research Council MC_UP_1202/12NIAID NIH HHS R01 AI025780NIAID NIH HHS R01 AI092084NIAID NIH HHS R01 AI097519NIAID NIH HHS R01 AI132638NIAID NIH HHS R01 AI136529NIAID NIH HHS R01 AI139615Wellcome Trust FC001076
6 · The paper itself

Abstract

The tetraspanin CD82 is a potent suppressor of tumor metastasis and regulates several processes including signal transduction, cell adhesion, motility, and aggregation. However, the mechanisms by which CD82 participates in innate immunity are unknown. We report that CD82 is a key regulator of TLR9 trafficking and signaling. TLR9 recognizes unmethylated cytosine-phosphate-guanine (CpG) motifs present in viral, bacterial, and fungal DNA. We demonstrate that TLR9 and CD82 associate in macrophages, which occurs in the endoplasmic reticulum (ER) and post-ER. Moreover, CD82 is essential for TLR9-dependent myddosome formation in response to CpG stimulation. Finally, CD82 modulates TLR9-dependent NF-κB nuclear translocation, which is critical for inflammatory cytokine production. To our knowledge, this is the first time a tetraspanin has been implicated as a key regulator of TLR signaling. Collectively, our study demonstrates that CD82 is a specific regulator of TLR9 signaling, which may be critical in cancer immunotherapy approaches and coordinating the innate immune response to pathogens.-Khan, N. S., Lukason, D. P., Feliu, M., Ward, R. A., Lord, A. K., Reedy, J. L., Ramirez-Ortiz, Z. G., Tam, J. M., Kasperkovitz, P. V., Negoro, P. E., Vyas, T. D., Xu, S., Brinkmann, M. M., Acharaya, M., Artavanis-Tsakonas, K., Frickel, E.-M., Becker, C. E., Dagher, Z., Kim, Y.-M., Latz, E., Ploegh, H. L., Mansour, M. K., Miranti, C. K., Levitz, S. M., Vyas, J. M. CD82 controls CpG-dependent TLR9 signaling.

Indexed as

Active Transport, Cell NucleusAnimalsCell NucleusCytokinesEndoplasmic ReticulumInflammationKangai-1 ProteinMacrophagesMiceMice, KnockoutNF-kappa BOligodeoxyribonucleotidesRAW 264.7 CellsSignal TransductionToll-Like Receptor 9Cd82 antigen, mouseCPG-oligonucleotideCytokinesKangai-1 ProteinNF-kappa BOligodeoxyribonucleotidesTlr9 protein, mouseToll-Like Receptor 9macrophagesmyddosometetraspaninsTLRs

Identifiers

PMID31408613
PMCPMC6988855
OpenAlexW2967420180

What OpenQuestion holds

Textmetadata
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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 OpenQuestion graph.