Evidence map›Paper›PMID 41530195›Full record

ArticleNature communications2026

A centrally positioned cluster of multiple centrioles in antigen-presenting cells fosters T cell activation.

Isabel Stötzel, Ann-Kathrin Weier, Apurba Sarkar, Subhendu Som, Luisa Bach, Peter Konopka, Eliška Miková, Shaunak Ghosh, Jan Böthling, Mirka Homrich and 13 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

23 authors.

Isabel StötzelLife and Medical Sciences (LIMES) Institute, Immune and Tumor Biology, University of Bonn, Bonn, Germany.ORCID http://orcid.org/0000-0001-6326-1409
Ann-Kathrin WeierLife and Medical Sciences (LIMES) Institute, Immune and Tumor Biology, University of Bonn, Bonn, Germany.ORCID http://orcid.org/0000-0003-2700-1102
Apurba SarkarSchool of Mathematical & Computational Sciences, Indian Association for the Cultivation of Science, Kolkata, West Bengal, India.ORCID http://orcid.org/0000-0003-0792-3089
Subhendu SomSchool of Mathematical & Computational Sciences, Indian Association for the Cultivation of Science, Kolkata, West Bengal, India.
Luisa BachMedical Clinic III for Oncology, Hematology, Immuno-Oncology and Rheumatology, University Hospital Bonn, University of Bonn, Venusberg-Campus 1, Bonn, Germany.ORCID http://orcid.org/0000-0002-3476-6325
Peter KonopkaLife and Medical Sciences (LIMES) Institute, Immune and Tumor Biology, University of Bonn, Bonn, Germany.
Eliška MikováBIOCEV, First Faculty of Medicine, Charles University, Vestec, Czech Republic.ORCID http://orcid.org/0000-0002-0829-992X
Shaunak GhoshLife and Medical Sciences (LIMES) Institute, Immune and Tumor Biology, University of Bonn, Bonn, Germany.ORCID http://orcid.org/0000-0002-8760-715X
Jan BöthlingLife and Medical Sciences (LIMES) Institute, Immune and Tumor Biology, University of Bonn, Bonn, Germany.ORCID http://orcid.org/0009-0008-9141-6461
Mirka HomrichLife and Medical Sciences (LIMES) Institute, Immune and Tumor Biology, University of Bonn, Bonn, Germany.ORCID http://orcid.org/0000-0003-0539-5198
Laura SchaedelDepartment of Experimental Physics and Center for Biophysics, Saarland University, Saarbrücken, Germany.ORCID http://orcid.org/0000-0002-7317-3696
Uli KazmaierOrganic Chemistry, Saarland University, Saarbrücken, Germany.ORCID http://orcid.org/0000-0001-9756-0589
Konstantinos SymeonidisInstitute of Experimental Immunology, University Hospital of Bonn, Bonn, Germany.
Stefan EbnerInstitute of Innate Immunity, Department for Systems Immunology and Proteomics, Medical Faculty, University of Bonn, Bonn, Germany.
Philip WeidnerDepartment of Internal Medicine 3 - Rheumatology and Immunology, Deutsches Zentrum für Immuntherapie (DZI), Friedrich-Alexander University Erlangen-Nürnberg (FAU) and Universitätsklinikum Erlangen, Erlangen, Germany.ORCID http://orcid.org/0009-0006-2327-5375
Zeinab AbdullahInstitute of Experimental Immunology, University Hospital of Bonn, Bonn, Germany.
Felix MeissnerInstitute of Innate Immunity, Department for Systems Immunology and Proteomics, Medical Faculty, University of Bonn, Bonn, Germany.ORCID http://orcid.org/0000-0003-1000-7989
Stefan UderhardtDepartment of Internal Medicine 3 - Rheumatology and Immunology, Deutsches Zentrum für Immuntherapie (DZI), Friedrich-Alexander University Erlangen-Nürnberg (FAU) and Universitätsklinikum Erlangen, Erlangen, Germany.ORCID http://orcid.org/0000-0002-2489-2109
Miroslav HonsBIOCEV, First Faculty of Medicine, Charles University, Vestec, Czech Republic.
Dirk BaumjohannMedical Clinic III for Oncology, Hematology, Immuno-Oncology and Rheumatology, University Hospital Bonn, University of Bonn, Venusberg-Campus 1, Bonn, Germany.ORCID http://orcid.org/0000-0001-8385-8288
Raja PaulSchool of Mathematical & Computational Sciences, Indian Association for the Cultivation of Science, Kolkata, West Bengal, India.ORCID http://orcid.org/0000-0001-7045-8584
Heiko RiegerDepartment of Theoretical Physics and Center for Biophysics, Saarland University, Saarbrücken, Germany. heiko.rieger@uni-saarland.de.ORCID http://orcid.org/0000-0003-0205-3678
Eva KiermaierLife and Medical Sciences (LIMES) Institute, Immune and Tumor Biology, University of Bonn, Bonn, Germany. eva.kiermaier@uni-bonn.de.ORCID http://orcid.org/0000-0001-6165-5738

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) EXC 2151 - 390873048
6 · The paper itself

Abstract

Cellular polarization plays a crucial role in regulating immunological processes and is often associated with reorientation of the centrosome. During immune synapse formation, centrosome repositioning in lymphocytes assists in T cell activation. While a single centrosome, consisting of two centrioles, is present in T cells, antigen-presenting cells such as dendritic cells amplify centrioles during maturation and immune activation. How centriole amplification in antigen-presenting cells affects immune synapse formation and T cell activation is unclear. In this study, we combine experimental data with mathematical and computational modelling to provide evidence that extra centrioles in dendritic cells form over-active microtubule organizing centers, which cluster during dendritic cell-T cell interactions and, unlike in T cells, localize close to the cell center. Perturbing either centrosome integrity or centriole numbers and configuration in dendritic cells results in impaired T cell activation. Collectively, our results highlight a crucial role for centriole amplification and optimal centrosome positioning in antigen-presenting cells for controlling T cell responses.

Indexed as

Antigen-Presenting CellsCentriolesDendritic CellsLymphocyte ActivationT-LymphocytesAnimalsCentrosomeHumansImmunological SynapsesMiceMicrotubule-Organizing Center

Identifiers

PMID41530195
PMCPMC12804990

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.