Evidence map›Paper›PMID 34630435›Full record

ArticleFrontiers in immunology2021

Ubiquitin Ligases CBL and CBL-B Maintain the Homeostasis and Immune Quiescence of Dendritic Cells.

Haijun Tong, Xin Li, Jinping Zhang, Liying Gong, Weili Sun, Virginie Calderon, Xiaochen Zhang, Yue Li, Adeline Gadzinski, Wallace Y Langdon and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Lipid metabolism in homeostasis and disease.Signal transduction and targeted therapy · 2026
    Review
  2. Article
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  8. Crosstalk of ubiquitin system and non-coding RNA in fibrosis.International journal of biological sciences · 2024
    Review
  9. Article
  10. 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

13 authors at 7 institutions in 4 countries.

Haijun TongMolecular Immunology Research Unit, Montreal Clinic Research Institute, Montreal, QC, Canada.
Xin LiMolecular Immunology Research Unit, Montreal Clinic Research Institute, Montreal, QC, Canada.
Jinping ZhangInstitute of Biology and Medical Science, SooChow University, Jiangsu, China.
Liying GongMolecular Immunology Research Unit, Montreal Clinic Research Institute, Montreal, QC, Canada.
Weili SunMolecular Immunology Research Unit, Montreal Clinic Research Institute, Montreal, QC, Canada.
Virginie CalderonMolecular Immunology Research Unit, Montreal Clinic Research Institute, Montreal, QC, Canada.
Xiaochen ZhangMolecular Immunology Research Unit, Montreal Clinic Research Institute, Montreal, QC, Canada.
Yue LiMolecular Immunology Research Unit, Montreal Clinic Research Institute, Montreal, QC, Canada.
Adeline GadzinskiMolecular Immunology Research Unit, Montreal Clinic Research Institute, Montreal, QC, Canada.
Wallace Y LangdonSchool of Biomedical Sciences, University of Western Australia, Crawley, WA, Australia.
Boris ReizisDepartment of Pathology, New York University Langone Medical Center, New York, NY, United States.
Yongrui ZouThe Feinstein Institute for Medical Research, Manhasset, New York, NY, United States.
Hua GuMolecular Immunology Research Unit, Montreal Clinic Research Institute, Montreal, QC, Canada.
Montreal Clinical Research Institute · CAFeinstein Institute for Medical Research · USMcGill University · CANYU Langone Health · USSoochow University · CNUniversité de Montréal · CAUniversity of Western Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dendritic cells (DCs) are composed of multiple lineages of hematopoietic cells and orchestrate immune responses upon detecting the danger and inflammatory signals associated with pathogen and damaged tissues. Under steady-state, DCs are maintained at limited numbers and the functionally quiescent status. While it is known that a fine balance in the DC homeostasis and activation status is also important to prevent autoimmune diseases and hyperinflammation, mechanisms that control DC development and activation under stead-state remain not fully understood. Here we show that DC-specific ablation of CBL and CBL-B (CBL

Indexed as

Adaptor Proteins, Signal TransducingAnimalsAntigen PresentationCell DivisionCells, CulturedCytokinesDendritic Cellsfms-Like Tyrosine Kinase 3Hepatitis, AutoimmuneHomeostasisLymphocyte SubsetsMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicPoint MutationAdaptor Proteins, Signal TransducingAkt1 protein, mouseCblb protein, mouseCbl protein, mouseCytokinesFlt3 protein, mousefms-Like Tyrosine Kinase 3Proto-Oncogene Proteins c-aktProto-Oncogene Proteins c-cblSirolimusdendritic cell (DC)E3 ubiquitin ligaseFLT3homeostasisliver inflammation

Identifiers

PMID34630435
PMCPMC8494778
OpenAlexW3203096781

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.