Evidence map›Paper›PMID 35969760›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

Chromatin structure undergoes global and local reorganization during murine dendritic cell development and activation.

Daisuke Kurotaki, Kenta Kikuchi, Kairong Cui, Wataru Kawase, Keita Saeki, Junpei Fukumoto, Akira Nishiyama, Kisaburo Nagamune, Keji Zhao, Keiko Ozato and 2 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

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  14. A lncRNA identifieseLife · 2023
    Article
  15. Dendritic cells in inborn errors of immunity.Frontiers in immunology · 2023
    Review
  16. Chromatin structure undergoes global and local reorganization during murine dendritic cell development and activation.Proceedings of the National Academy of Sciences of the United States of America · 2022
    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

12 authors at 7 institutions in 2 countries.

Daisuke KurotakiLaboratory of Chromatin Organization in Immune Cell Development, International Research Center for Medical Sciences, Kumamoto University, Kumamoto 860-0811, Japan.ORCID 0000-0002-4728-0113
Kenta KikuchiLaboratory of Chromatin Organization in Immune Cell Development, International Research Center for Medical Sciences, Kumamoto University, Kumamoto 860-0811, Japan.ORCID 0000-0002-6084-7559
Kairong CuiLaboratory of Epigenome Biology, Systems Biology Center, National Heart, Lung, and Blood Institute, NIH, Bethesda, MD 20814.
Wataru KawaseDepartment of Immunology, Yokohama City University Graduate School of Medicine, Yokohama 236-0004, Japan.ORCID 0000-0002-1670-3806
Keita SaekiProgram in Genomics of Differentiation, Eunice Kennedy Shriver National Institute of Child Health and Human Development, NIH, Bethesda, MD 20892.ORCID 0000-0002-0611-176X
Junpei FukumotoDepartment of Parasitology, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Akira NishiyamaDepartment of Immunology, Yokohama City University Graduate School of Medicine, Yokohama 236-0004, Japan.
Kisaburo NagamuneDepartment of Parasitology, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.ORCID 0000-0003-0212-6726
Keji ZhaoLaboratory of Epigenome Biology, Systems Biology Center, National Heart, Lung, and Blood Institute, NIH, Bethesda, MD 20814.
Keiko OzatoProgram in Genomics of Differentiation, Eunice Kennedy Shriver National Institute of Child Health and Human Development, NIH, Bethesda, MD 20892.ORCID 0000-0001-7013-2728
Pedro P RochaUnit on Genome Structure and Regulation, Eunice Kennedy Shriver National Institute of Child Health and Human Development, NIH, Bethesda, MD 20892.ORCID 0000-0003-4691-7773
Tomohiko TamuraDepartment of Immunology, Yokohama City University Graduate School of Medicine, Yokohama 236-0004, Japan.ORCID 0000-0002-9664-1747
Yokohama City University · JPEunice Kennedy Shriver National Institute of Child Health and Human Development · USNational Heart Lung and Blood Institute · USNational Institute of Infectious Diseases · JPKumamoto University · JPNational Cancer Institute · USYokohama City University Medical Center · JP

Funding

Epigenetic Regulation of Hematopoietic Stem CellsZIAHL006031 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI ZHAO, KEJI · 2009 to 2025
$16.6M
Epigenetic Regulation of T cell differentiationZIAHL006030 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI ZHAO, KEJI · 2009 to 2025
$15.3M
Genome 3D organization as a determinant of cell-fate decisionsZIAHD008975 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI ROCHA, PEDRO · 2018 to 2025
$10.4M
6 · The paper itself

Abstract

Classical dendritic cells (cDCs) are essential for immune responses and differentiate from hematopoietic stem cells via intermediate progenitors, such as monocyte-DC progenitors (MDPs) and common DC progenitors (CDPs). Upon infection, cDCs are activated and rapidly express host defense-related genes, such as those encoding cytokines and chemokines. Chromatin structures, including nuclear compartments and topologically associating domains (TADs), have been implicated in gene regulation. However, the extent and dynamics of their reorganization during cDC development and activation remain unknown. In this study, we comprehensively determined higher-order chromatin structures by Hi-C in DC progenitors and cDC subpopulations. During cDC differentiation, chromatin activation was initially induced at the MDP stage. Subsequently, a shift from inactive to active nuclear compartments occurred at the cDC gene loci in CDPs, which was followed by increased intra-TAD interactions and loop formation. Mechanistically, the transcription factor IRF8, indispensable for cDC differentiation, mediated chromatin activation and changes into the active compartments in DC progenitors, thereby possibly leading to cDC-specific gene induction. Using an infection model, we found that the chromatin structures of host defense-related gene loci were preestablished in unstimulated cDCs, indicating that the formation of higher-order chromatin structures prior to infection may contribute to the rapid responses to pathogens. Overall, these results suggest that chromatin structure reorganization is closely related to the establishment of cDC-specific gene expression and immune functions. This study advances the fundamental understanding of chromatin reorganization in cDC differentiation and activation.

Indexed as

Chromatin Assembly and DisassemblyDendritic CellsHematopoietic Stem CellsAnimalsCell DifferentiationChromatinGene Expression RegulationMiceChromatinchromatin structuredendritic cellhematopoiesisinfectiontranscription factor

Identifiers

PMID35969760
PMCPMC9407307
OpenAlexW4291652221

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.