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Projekt Druckansicht

Molekulare und zelluläre Veränderungen während der Fibroseentwicklung bei Kardiomyopathien

Antragsteller Dr. Daniel Reichart
Fachliche Zuordnung Kardiologie, Angiologie
Förderung Förderung von 2018 bis 2020
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 413001050
 
Erstellungsjahr 2021

Zusammenfassung der Projektergebnisse

Single cell RNA sequencing (scRNAseq) has helped to gain deeper insights into the cellular compositions of organs by specific cell type and cell state (cell sub-types) characterization. Single nuclei RNA sequencing (snRNAseq) demonstrates several advantages over scRNAseq: frozen tissues can be used for nuclei isolation, snRNAseq is more robust in terms of technical artefacts and – most importantly - snRNAseq allows to analyze cardiomyocytes since the average nuclei diameter of 7-12µm makes them suitable for droplet-based single cells/nuclei machines. During my stay in the lab of Christine and Jonathan Seidman, snRNAseq was used to re-map the healthy human heart cell-by-cell. Approximately 500K nuclei and cells were isolated from transmural heart biopsies of 14 healthy donor hearts (7 female, 7 male) for snRNAseq and scRNAseq. Six regions covering left and right ventricular free wall, septum, apex, left and right atrium were included and helped to identify gene expression patterns of 11 major cell types and 65 cell states. These results highlight the heterogeneity of cardiomyocytes, fibroblasts, and others cell types in terms of their regional distribution, distinct gene expressions and functional states. To confirm specific findings and investigate gene expression patterns across the tissues, multiplex fluorescent RNA in-situ hybridizations were performed. This atlas at single cell level of the healthy human heart lays the ground for additional studies involving diseased tissues or perturbation models and will further add to the knowledge of pathologic molecular mechanisms.

Projektbezogene Publikationen (Auswahl)

 
 

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