Spatial omics of acute myocardial infarction reveals a novel mode of immune cell infiltration

F. Sicklinger (Heidelberg)¹, F. Wünnemann (Heidelberg)², K. Bestak (Heidelberg)², J. Nimo (Berlin)³, J. Amrute (St. Louis)⁴, T. Thiemann (Heidelberg)¹, N. Hartmann (Heidelberg)¹, N. Frey (Heidelberg)¹, K. Lavine (St. Louis)⁴, F. Coscia (Berlin)³, D. Schapiro (Heidelberg)², F. Leuschner (Heidelberg)^1
1Universitätsklinikum Heidelberg Klinik für Innere Med. III, Kardiologie, Angiologie u. Pneumologie Heidelberg, Deutschland; ²Institute for Computational Biomedicine, Heidelberg University Heidelberg, Deutschland; ³Max-Delbrück-Centrum für Molekulare Medizin Berlin, Deutschland; ⁴Center for Cardiovascular Research, Department of Medicine, Cardiovascular Division, Washington University School of Medicine, St. Louis, USA

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. Here 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), which enabled us to evaluate cell-type compositions and changes at subcellular resolution over time. One striking finding of these analyses was the identification of a novel mode of leukocyte accumulation to the infarcted heart via the endocardium. To investigate the underlying mechanisms driving this previously unknown infiltration route, we performed unbiased spatial proteomic analysis using Deep Visual Proteomics (DVP). When comparing endocardial cells of homeostatic hearts and infarcted hearts, DVP identified von Willebrand Factor (vWF) as an upregulated mediator of inflammation 24 hours post-MI. To further explore the immune mediating capabilities of vWF and its effect on tissue repair, we performed functional blocking of vWF during acute murine MI. This resulted in a reduced amount of infiltration by CCR2+ monocytes and worse cardiac function post-MI. Our study provides the first spatial map of acute murine MI with subcellular resolution and subsequently discovers a novel route of immune infiltration. Furthermore, we identified vWF as a critical immune mediating agent for endocardial immune cell infiltration.