Spatial multi-omic map of human myocardial infarction

Christoph Kuppe, Ricardo O. Ramirez Flores, Zhijian Li, Sikander Hayat, Rebecca T. Levinson, Xian Liao, Monica T. Hannani, Jovan Tanevski, Florian Wünnemann, James S. Nagai, Maurice Halder, David Schumacher, Sylvia Menzel, Gideon Schäfer, Konrad Hoeft, Mingbo Cheng, Susanne Ziegler, Xiaoting Zhang, Fabian Peisker, Nadine Kaesler, Turgay Saritas, Yaoxian Xu, Astrid Kassner, Jan Gummert, Michiel Morshuis, Junedh Amrute, Rogier J. A. Veltrop, Peter Boor, Karin Klingel, Linda W. Van Laake, Aryan Vink, Remco M. Hoogenboezem, Eric M. J. Bindels, Leon Schurgers, Susanne Sattler, Denis Schapiro, Rebekka K. Schneider, Kory Lavine, Hendrik Milting, Ivan G. Costa, Julio Saez-Rodriguez, Rafael Kramann

Abstract

Myocardial infarction is a leading cause of death worldwide1. Although advances have been made in acute treatment, an incomplete understanding of remodelling processes has limited the effectiveness of therapies to reduce late-stage mortality2. Here we generate an integrative high-resolution map of human cardiac remodelling after myocardial infarction using single-cell gene expression, chromatin accessibility and spatial transcriptomic profiling of multiple physiological zones at distinct time points in myocardium from patients with myocardial infarction and controls. Multi-modal data integration enabled us to evaluate cardiac cell-type compositions at increased resolution, yielding insights into changes of the cardiac transcriptome and epigenome through the identification of distinct tissue structures of injury, repair and remodelling. We identified and validated disease-specific cardiac cell states of major cell types and analysed them in their spatial context, evaluating their dependency on other cell types. Our data elucidate the molecular principles of human myocardial tissue organization, recapitulating a gradual cardiomyocyte and myeloid continuum following ischaemic injury. In sum, our study provides an integrative molecular map of human myocardial infarction, represents an essential reference for the field and paves the way for advanced mechanistic and therapeutic studies of cardiac disease.

Datasets

1. All-snRNA-Spatial multi-omic map of human myocardial infarction
Metadata
sample
cell_type_original
patient_region_id
donor_id
patient_group
major_labl
final_cluster
assay_ontology_term_id
development_stage_ontology_term_id
disease_ontology_term_id
self_reported_ethnicity_ontology_term_id
organism_ontology_term_id
sex_ontology_term_id
tissue_ontology_term_id
cell_type_ontology_term_id
suspension_type
tissue_type
cell_type
assay
disease
organism
sex
tissue
self_reported_ethnicity
development_stage
CK36014562 cells
CK15811416 cells
CK35611250 cells
CK16310910 cells
CK35810873 cells
CK16410795 cells
CK35710682 cells
CK35910399 cells
CK1599817 cells
CK1609301 cells
CK3748692 cells
CK3668567 cells
CK3646279 cells
CK3626256 cells
CK3686140 cells
CK3616043 cells
CK3675306 cells
CK3715026 cells
CK3734339 cells
CK3633898 cells
CK3653654 cells
CK3703453 cells
CK3723166 cells
CK3752801 cells
CK1622619 cells
CK1651897 cells
CK3691783 cells
CK3761290 cells
CK161581 cells
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Spatial multi-omic map of human myocardial infarction

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Source data

https://cellxgene.cziscience.com/collections/8191c283-0816-424b-9b61-c3e1d6258a77

Alias names

EGAS00001006330, PMID35948637, PMC9364862

Cite this study

Kuppe, C., Ramirez Flores, R.O., Li, Z., Hayat, S., Levinson, R.T., Liao, X., Hannani, M.T., Tanevski, J., Wünnemann, F., Nagai, J.S. and Halder, M., 2022. Spatial multi-omic map of human myocardial infarction. Nature, 608(7924), pp.766-777. https://doi.org/10.1038/s41586-022-05060-x