Myeloid cell recruitment propels right ventricular dysfunction in HFpEF via sterile inflammation
Ontology highlight
ABSTRACT: This project characterizes chamber-specific proteomic remodeling in a murine three-hit HFpEF model that develops right ventricular dysfunction, using chow, hypoxia alone, and HFD+L-NAME as control conditions. The three-hit model (hypoxia, high-fat diet, and L-NAME) recapitulates key features of human HFpEF, including left ventricular diastolic dysfunction and secondary right ventricular hypertrophy and dysfunction.
INSTRUMENT(S):
ORGANISM(S): Mus Musculus (mouse)
TISSUE(S): Heart
DISEASE(S): Heart Failure
SUBMITTER:
Pauline Fahjen
LAB HEAD: Philipp Mertins
PROVIDER: PXD074772 | Pride | 2026-09-07
REPOSITORIES: Pride
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