Evidence map›Paper›PMID 38822080›Full record

ArticleCellular & molecular immunology2024

TRIM33 plays a critical role in regulating dendritic cell differentiation and homeostasis by modulating Irf8 and Bcl2l11 transcription.

Xiangyi Shen, Xiaoguang Li, Tao Wu, Tingting Guo, Jiaoyan Lv, Zhimin He, Maocai Luo, Xinyi Zhu, Yujie Tian, Wenlong Lai and 3 more

Abstract read
In one paragraph

Article in Cellular & molecular immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. 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.

Xiangyi Shen *Institute for Immunology, School of Basic Medical Sciences, Tsinghua University, 100084, Beijing, China.ORCID 0000-0002-7460-1066
Xiaoguang Li *Institute for Immunology, School of Basic Medical Sciences, Tsinghua University, 100084, Beijing, China.
Tao Wu *Institute for Immunology, School of Basic Medical Sciences, Tsinghua University, 100084, Beijing, China.
Tingting GuoInstitute for Immunology, School of Basic Medical Sciences, Tsinghua University, 100084, Beijing, China.
Jiaoyan LvInstitute for Immunology, School of Basic Medical Sciences, Tsinghua University, 100084, Beijing, China.
Zhimin HeInstitute for Immunology, School of Basic Medical Sciences, Tsinghua University, 100084, Beijing, China.
Maocai LuoInstitute for Immunology, School of Basic Medical Sciences, Tsinghua University, 100084, Beijing, China.
Xinyi ZhuInstitute for Immunology, School of Basic Medical Sciences, Tsinghua University, 100084, Beijing, China.
Yujie TianInstitute for Immunology, School of Basic Medical Sciences, Tsinghua University, 100084, Beijing, China.
Wenlong LaiInstitute for Immunology, School of Basic Medical Sciences, Tsinghua University, 100084, Beijing, China.
Chen DongInstitute for Immunology, School of Basic Medical Sciences, Tsinghua University, 100084, Beijing, China.ORCID 0000-0002-0084-9130
Xiaoyu HuInstitute for Immunology, School of Basic Medical Sciences, Tsinghua University, 100084, Beijing, China.ORCID 0000-0002-4289-6998
Li WuInstitute for Immunology, School of Basic Medical Sciences, Tsinghua University, 100084, Beijing, China. wuli@tsinghua.edu.cn.

Funding

Ministry of Science and Technology of the People's Republic of China (Chinese Ministry of Science and Technology) 2019YFA0508502Ministry of Science and Technology of the People's Republic of China (Chinese Ministry of Science and Technology) 2022YFC2505001National Natural Science Foundation of China (National Science Foundation of China) 31800769National Natural Science Foundation of China (National Science Foundation of China) 31991174National Natural Science Foundation of China (National Science Foundation of China) 81801641National Natural Science Foundation of China (National Science Foundation of China) 82388101
6 · The paper itself

Abstract

The development of distinct dendritic cell (DC) subsets, namely, plasmacytoid DCs (pDCs) and conventional DC subsets (cDC1s and cDC2s), is controlled by specific transcription factors. IRF8 is essential for the fate specification of cDC1s. However, how the expression of Irf8 is regulated is not fully understood. In this study, we identified TRIM33 as a critical regulator of DC differentiation and maintenance. TRIM33 deletion in Trim33

Indexed as

Bcl-2-Like Protein 11Cell DifferentiationDendritic CellsHomeostasisInterferon Regulatory FactorsMice, Inbred C57BLTranscription FactorsAnimalsApoptosisCyclin-Dependent Kinase 9Hematopoietic Stem CellsInterferon Regulatory Factor-8MiceMice, KnockoutProto-Oncogene ProteinsProto-Oncogene Protein Spi-1Bcl-2-Like Protein 11Cdk9 protein, mouseCyclin-Dependent Kinase 9Interferon Regulatory Factor-8Interferon Regulatory FactorsProto-Oncogene ProteinsProto-Oncogene Protein Spi-1RNA Polymerase IITrans-ActivatorsTranscription FactorsTrim33 protein, mouseBIMDendritic cellIRF8Transcription regulationTRIM33

Identifiers

PMID38822080
PMCPMC11214632

What OpenQuestion holds

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Registered trials

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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.