Analysis of cellular NO-GC expression in the murine heart and lineage determination in angiotensin II-induced fibrosis

NO-sensitive guanylyl cyclase (NO-GC) is involved in the (patho)physiology of the mammalian heart. However, little is known about the individual cardiac cell types that express NO-GC and the role of the enzyme in cardiac fibrosis. Here, we describe the cellular expression of NO-GC in healthy and fibrotic murine myocardium; these data were compared with scRNA-seq data. In healthy myocardium, NO-GC is strongly expressed in pericytes and smooth muscle cells but not in endothelial cells or cardiomyocytes. Angiotensin II induced cardiac hypertrophy and fibrosis; fibrotic lesions contained cells positive for NO-GC identified as activated fibroblasts. Lineage tracing indicates that NO-GC-expressing activated fibroblasts originate from PDGFRβ- and Tcf21-positive fibroblast precursors. Our data indicate NO-GC expression in cardiac pericytes and SMC in naive myocardium and in activated fibroblast in fibrotic heart tissue. NO-mediated signaling may modulate fibrotic responses underlying the action of NO-GC stimulators used in the therapy of heart failure.

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Journal
iScience
Published
2024-12-16
DOI
https://doi.org/10.1016/j.isci.2024.111615
Primary Topic
Cardiac Fibrosis and Remodeling
Type
article
Field-Weighted Citation Impact
0.00

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article

Analysis of cellular NO-GC expression in the murine heart and lineage determination in angiotensin II-induced fibrosis

Alexander R. Pinto, Andreas Friebe, Malathi Dona, Michelle D. Tallquist et al.
1 links
iScience
Cardiac Fibrosis and Remodeling
article

Analysis of cellular NO-GC expression in the murine heart and lineage determination in angiotensin II-induced fibrosis

Alexander R. Pinto, Andreas Friebe, Malathi Dona, Michelle D. Tallquist, Annika Gaab, Dieter Groneberg, Lennart Kreutz
article en

Abstract

NO-sensitive guanylyl cyclase (NO-GC) is involved in the (patho)physiology of the mammalian heart. However, little is known about the individual cardiac cell types that express NO-GC and the role of the enzyme in cardiac fibrosis. Here, we describe the cellular expression of NO-GC in healthy and fibrotic murine myocardium; these data were compared with scRNA-seq data. In healthy myocardium, NO-GC is strongly expressed in pericytes and smooth muscle cells but not in endothelial cells or cardiomyocytes. Angiotensin II induced cardiac hypertrophy and fibrosis; fibrotic lesions contained cells positive for NO-GC identified as activated fibroblasts. Lineage tracing indicates that NO-GC-expressing activated fibroblasts originate from PDGFRβ- and Tcf21-positive fibroblast precursors. Our data indicate NO-GC expression in cardiac pericytes and SMC in naive myocardium and in activated fibroblast in fibrotic heart tissue. NO-mediated signaling may modulate fibrotic responses underlying the action of NO-GC stimulators used in the therapy of heart failure.

iScienceVol. 28(1)
University of Hawaiʻi at Mānoa (US), Baker Heart and Diabetes Institute (AU), University of Würzburg (DE), Fraunhofer Institute for Silicate Research (DE)
National Heart Foundation of Australia, Deutsche Forschungsgemeinschaft
Zero hunger
Openalex Percentile: Top 58%
Cardiac Fibrosis and Remodeling
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Analysis of cellular NO-GC expression in the murine heart and lineage determination in angiotensin II-induced fibrosis — Alexander R. Pinto, Andreas Friebe, et al. · iScience (2024) | TGRS Research Map | TGRS