Evidence map›Paper›PMID 39838105›Full record

ArticleNature immunology2025

Cholesterol mobilization regulates dendritic cell maturation and the immunogenic response to cancer.

Meriem Belabed, Matthew D Park, Cédric M Blouin, Sreekumar Balan, Chang Y Moon, Grace Freed, Miguel Quijada-Álamo, Ante Peros, Raphaël Mattiuz, Amanda M Reid and 20 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed.

  1. Article
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  4. Caveolae mechanics in cellular functions and disease.Nature reviews. Molecular cell biology · 2026
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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

30 authors.

Meriem Belabed *Marc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID http://orcid.org/0000-0002-3210-1581
Matthew D Park *Marc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Cédric M BlouinMembrane Mechanics and Dynamics of Intracellular Signaling Laboratory, Centre de Recherche, Institut Curie, PSL Research University, Paris, France.ORCID http://orcid.org/0000-0003-0800-0948
Sreekumar BalanMarc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID http://orcid.org/0000-0002-2092-5145
Chang Y MoonMarc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Grace FreedThe Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Miguel Quijada-ÁlamoThe Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Ante PerosMarc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Raphaël MattiuzMarc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID http://orcid.org/0000-0002-3292-1635
Amanda M ReidMarc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Nader YatimMarc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Jesse BoumelhaMarc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Camillia S AzimiMarc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Nelson M LaMarcheMarc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Leanna TroncosoMarc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID http://orcid.org/0000-0003-2529-9267
Angelo AmabileMarc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Jessica Le BerichelMarc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Steven T ChenMarc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
C Matthias WilkMarc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID http://orcid.org/0000-0001-5429-7143
Brian D BrownMarc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID http://orcid.org/0000-0002-3670-8778
Kristen J RadfordMater Research Institute, the University of Queensland, Brisbane, Queensland, Australia.ORCID http://orcid.org/0000-0001-6512-6323
Sourav GhoshDepartment of Immunobiology and Department of Pharmacology, Yale School of Medicine, Yale University, New Haven, CT, USA.ORCID http://orcid.org/0000-0001-5990-8708
Carla V RothlinDepartment of Neurology and Department of Pharmacology, Yale School of Medicine, Yale University, New Haven, CT, USA.ORCID http://orcid.org/0000-0002-5693-5572
Laurent Yvan-CharvetINSERM U1065, ATIP-Avenir, Fédération Hospitalo-Universitaire OncoAge, Université Côte d'Azur, Centre Méditerranéen de Médecine Moléculaire (C3M), Nice, France.ORCID http://orcid.org/0000-0002-7748-4942
Thomas U MarronMarc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID http://orcid.org/0000-0001-5903-8191
Daniel J PulestonMarc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID http://orcid.org/0000-0002-8437-0732
Elvin WagenblastThe Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID http://orcid.org/0000-0002-0709-2759
Nina BhardwajMarc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID http://orcid.org/0000-0003-1865-4187
Christophe LamazeMembrane Mechanics and Dynamics of Intracellular Signaling Laboratory, Centre de Recherche, Institut Curie, PSL Research University, Paris, France.ORCID http://orcid.org/0000-0001-5430-2707
Miriam MeradMarc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA. miriam.merad@mssm.edu.ORCID http://orcid.org/0000-0002-4481-7827

Funding

Spatial functional genomics to identify regulators of the tumor microenvironment and cancer immunityU01CA282114 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Brian D Brown, MIRIAM MERAD · 2023 to 2026
$4.2M
Investigating Macrophage Molecular and Functional Diversity in Tumor ImmunityR01CA254104 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BROWN, BRIAN D, MERAD, MIRIAM · 2021 to 2025
$3.4M
Type 2 immunity: a primitive response to epithelial injury that shapes bone marrow and lung myeloid crosstalkR01CA277479 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI MIRIAM MERAD, Thomas Urban Marron · 2023 to 2026
$2.6M
NCI NIH HHS R01 CA277479U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) R01CA254104U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) R01CA277479U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) U01CA282114
6 · The paper itself

Abstract

Maturation of conventional dendritic cells (cDCs) is crucial for maintaining tolerogenic safeguards against auto-immunity and for promoting immunogenic responses to pathogens and cancer. The subcellular mechanism for cDC maturation remains poorly defined. We show that cDCs mature by leveraging an internal reservoir of cholesterol (harnessed from extracellular cell debris and generated by de novo synthesis) to assemble lipid nanodomains on cell surfaces of maturing cDCs, enhance expression of maturation markers and stabilize immune receptor signaling. This process is dependent on cholesterol transport through Niemann-Pick disease type C1 (NPC1) and mediates homeostatic and Toll-like receptor (TLR)-induced maturation. Importantly, we identified the receptor tyrosine kinase AXL as a regulator of the NPC1-dependent construction of lipid nanodomains. Deleting AXL from cDCs enhances their maturation, thus improving anti-tumor immunity. Altogether, our study presents new insights into cholesterol mobilization as a fundamental basis for cDC maturation and highlights AXL as a therapeutic target for modulating cDCs.

Indexed as

CholesterolDendritic CellsNeoplasmsAnimalsAxl Receptor Tyrosine KinaseCell DifferentiationHumansMiceMice, Inbred C57BLMice, KnockoutNiemann-Pick C1 ProteinProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesSignal TransductionToll-Like ReceptorsAxl Receptor Tyrosine KinaseCholesterolNiemann-Pick C1 ProteinProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesToll-Like Receptors

Identifiers

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.