Evidence map›Paper›PMID 41044418›Full record

ArticleNature cardiovascular research2025

Spatial multiomics of acute myocardial infarction reveals immune cell infiltration through the endocardium.

Florian Wünnemann, Florian Sicklinger, Kresimir Bestak, Jose Nimo, Tobias Thiemann, Junedh M Amrute, Mathias Nordbeck, Niklas Hartmann, Miguel A Ibarra-Arellano, Jovan Tanevski and 8 more

Abstract read
In one paragraph

Article in Nature cardiovascular research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Genetics-Informed Mapping Identifies a CRIM1-Associated Endocardial Inflammatory Remodeling State in Acute Myocardial Infarction.Medical science monitor : international medical journal of experimental and clinical research · 2026
    Article
  4. Article
  5. Review
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  7. Review
  8. Article
  9. Article
  10. Review
  11. Cardio-Vascular Extracellular Matrix: The Unmet Enigma.International journal of molecular sciences · 2026
    Review
  12. Article
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  15. Review
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

18 authors.

Florian Wünnemann *Institute for Computational Biomedicine, Faculty of Medicine, University Hospital Heidelberg and Heidelberg University, Heidelberg, Germany.
Florian Sicklinger *Department of Internal Medicine III, University Hospital Heidelberg, Heidelberg, Germany.ORCID http://orcid.org/0009-0004-6707-1695
Kresimir BestakInstitute for Computational Biomedicine, Faculty of Medicine, University Hospital Heidelberg and Heidelberg University, Heidelberg, Germany.ORCID http://orcid.org/0009-0009-8245-9846
Jose NimoMax Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Spatial Proteomics Group, Berlin, Germany.
Tobias ThiemannDepartment of Internal Medicine III, University Hospital Heidelberg, Heidelberg, Germany.ORCID http://orcid.org/0009-0003-7284-2127
Junedh M AmruteCenter for Cardiovascular Research, Department of Medicine, Cardiovascular Division, Washington University School of Medicine, St. Louis, MO, USA.ORCID http://orcid.org/0000-0002-6851-0168
Mathias NordbeckInstitute for Computational Biomedicine, Faculty of Medicine, University Hospital Heidelberg and Heidelberg University, Heidelberg, Germany.ORCID http://orcid.org/0009-0003-0392-6685
Niklas HartmannDepartment of Internal Medicine III, University Hospital Heidelberg, Heidelberg, Germany.ORCID http://orcid.org/0009-0009-1799-7162
Miguel A Ibarra-ArellanoInstitute for Computational Biomedicine, Faculty of Medicine, University Hospital Heidelberg and Heidelberg University, Heidelberg, Germany.ORCID http://orcid.org/0000-0001-8411-4854
Jovan TanevskiInstitute for Computational Biomedicine, Faculty of Medicine, University Hospital Heidelberg and Heidelberg University, Heidelberg, Germany.ORCID http://orcid.org/0000-0001-7177-1003
Margot ChazotteInstitute for Computational Biomedicine, Faculty of Medicine, University Hospital Heidelberg and Heidelberg University, Heidelberg, Germany.ORCID http://orcid.org/0009-0007-4901-5173
Clara HeineDepartment of Internal Medicine III, University Hospital Heidelberg, Heidelberg, Germany.ORCID http://orcid.org/0009-0001-3506-2119
Norbert FreyDepartment of Internal Medicine III, University Hospital Heidelberg, Heidelberg, Germany.
Kory J LavineCenter for Cardiovascular Research, Department of Medicine, Cardiovascular Division, Washington University School of Medicine, St. Louis, MO, USA.ORCID http://orcid.org/0000-0003-1948-9945
Fabian CosciaMax Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Spatial Proteomics Group, Berlin, Germany.ORCID http://orcid.org/0000-0002-2244-5081
Julio Saez-RodriguezInstitute for Computational Biomedicine, Faculty of Medicine, University Hospital Heidelberg and Heidelberg University, Heidelberg, Germany.ORCID http://orcid.org/0000-0002-8552-8976
Florian Leuschner *Department of Internal Medicine III, University Hospital Heidelberg, Heidelberg, Germany. florian.leuschner@med.uni-heidelberg.de.ORCID http://orcid.org/0000-0003-1157-474X
Denis Schapiro *Institute for Computational Biomedicine, Faculty of Medicine, University Hospital Heidelberg and Heidelberg University, Heidelberg, Germany. denis.schapiro@uni-heidelberg.de.ORCID http://orcid.org/0000-0002-9391-5722

Funding

Specification and Function of Tissue Resident and Recruited Macrophages in Cardiac Remodeling and Heart FailureR35HL161185 · NHLBI · WASHINGTON UNIVERSITY · PI Kory J. Lavine · 2022 to 2026
$4.3M
NHLBI NIH HHS R35 HL161185
6 · The paper itself

Abstract

Myocardial infarction (MI) continues to be a leading cause of death worldwide. Even though it is well established that the complex interplay between different cell types determines the overall healing response after MI, the precise changes in the tissue architecture are still poorly understood. In this study, we generated an integrative cellular map of the acute phase after murine MI using a combination of imaging-based transcriptomics (Molecular Cartography) and antibody-based highly multiplexed imaging (Sequential Immunofluorescence). This enabled us to evaluate cell type compositions and changes at subcellular resolution over time. We observed the recruitment of leukocytes to the infarcted heart through the endocardium and performed unbiased spatial proteomic analysis using Deep Visual Proteomics (DVP) to investigate the underlying mechanisms. DVP identified von Willebrand factor (vWF) as an upregulated mediator of inflammation 24 hours after MI, and functional blocking of vWF reduced the infiltration of C-C chemokine receptor 2 (Ccr2)-positive monocytes and worsened cardiac function after MI.

Indexed as

Chemotaxis, LeukocyteEndocardiumGene Expression ProfilingMonocytesMyocardial InfarctionMyocardiumProteomicsAnimalsDisease Models, AnimalMaleMiceMice, Inbred C57BLMultiomicsReceptors, CCR2Time FactorsTranscriptomeCcr2 protein, mouseReceptors, CCR2von Willebrand Factor

Identifiers

PMID41044418
PMCPMC12520975

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.