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ABSTRACT: Introduction
Despite the high morbidity and mortality, the effective therapies for heart failure with preserved fraction (HFpEF) are limited as the poor understand of its pathophysiological basis.Objective
This study was aimed to characterize the cellular heterogeneity and potential mechanisms of HFpEF at single-cell resolution.Methods
An HFpEF mouse model was induced by a high-fat diet with N-nitro-L-arginine methyl ester. Cells from the hearts were subjected to single-cell sequencing. The key protein expression was measured with Immunohistochemistry and immunofluorescence staining.Results
In HFpEF hearts, myocardial fibroblasts exhibited higher levels of fibrosis. Furthermore, an increased number of fibroblasts differentiated into high-metabolism and high-
SUBMITTER: Li G
PROVIDER: S-EPMC11785561 | biostudies-literature | 2025 Feb
REPOSITORIES: biostudies-literature