Evidence map›Paper›PMID 33318291›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2021

Ubiquitination of MHC Class II by March-I Regulates Dendritic Cell Fitness.

Hei Jung Kim, Joanna Bandola-Simon, Satoshi Ishido, Nathan W Wong, Vishal N Koparde, Maggie Cam, Paul A Roche

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

13 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Ubiquitination in cancer: mechanisms and therapeutic opportunities.Cancer communications (London, England) · 2025
    Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Antigen Presentation in the Lung.Frontiers in immunology · 2022
    Review
  12. Article
  13. Article
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

7 authors at 2 institutions in 2 countries.

Hei Jung KimExperimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
Joanna Bandola-SimonExperimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.ORCID 0000-0002-4908-7384
Satoshi IshidoDepartment of Microbiology, Hyogo College of Medicine, Nishinomiya 663-8501, Japan.
Nathan W WongCenter for Cancer Research Collaborative Bioinformatics Resource, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892; and.
Vishal N KopardeCenter for Cancer Research Collaborative Bioinformatics Resource, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892; and.
Maggie CamCenter for Cancer Research Collaborative Bioinformatics Resource, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892; and.
Paul A RocheExperimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892; paul.roche@nih.gov.ORCID 0000-0002-8949-9172
National Institutes of Health · USHyogo Medical University · JP

Funding

Application of Flow Cytometry to Cell BiologyZICBC009255 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI CROSSMAN, ASSIATU · 2009 to 2025
$26.4M
Regulation of MHC Class II Trafficking in Antigen Presenting CellsZIABC009404 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI ROCHE, PAUL · 2009 to 2025
$17.9M
Regulation of MHC Class II Trafficking in Antigen Presenting CellsZ01BC009404 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI ROCHE, PAUL · 1996 to 2008
$1.8M
CCR NIH HHS HHSN261200800001CIntramural NIH HHS Z01 BC009404NCI NIH HHS HHSN261200800001E
6 · The paper itself

Abstract

The expression and turnover of Ag-specific peptide-MHC class II (pMHC-II) on the surface of dendritic cells (DCs) is essential for their ability to efficiently activate CD4 T cells. Ubiquitination of pMHC-II by the E3 ubiquitin ligase March-I regulates surface expression and survival of pMHC-II in DCs. We now show that despite their high levels of surface pMHC-II, MHC class II (MHC-II) ubiquitination-deficient mouse DCs are functionally defective; they are poor stimulators of naive CD4 T cells and secrete IL-12 in response to LPS stimulation poorly. MHC-II ubiquitination-mutant DC defects are cell intrinsic, and single-cell RNA sequencing demonstrates that these DCs have an altered gene expression signature as compared with wild-type DCs. Curiously, these functional and gene transcription defects are reversed by activating the DCs with LPS. These results show that dysregulation of MHC-II turnover suppresses DC development and function.

Indexed as

AnimalsAntigen PresentationAntigensCD4-Positive T-LymphocytesCell DifferentiationCells, CulturedDendritic CellsHistocompatibility Antigens Class IIInterleukin-12Lymphocyte ActivationMiceMice, KnockoutUbiquitinationUbiquitin-Protein LigasesAntigensHistocompatibility Antigens Class IIInterleukin-12MARCH1 protein, mouseUbiquitin-Protein Ligases

Identifiers

PMID33318291
PMCPMC9169697
OpenAlexW3112606349

What OpenQuestion holds

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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.