Stabilization of Perivascular Mast Cells by Endothelial CNP (C-Type Natriuretic Peptide).


Journal

Arteriosclerosis, thrombosis, and vascular biology
ISSN: 1524-4636
Titre abrégé: Arterioscler Thromb Vasc Biol
Pays: United States
ID NLM: 9505803

Informations de publication

Date de publication:
03 2020
Historique:
pubmed: 3 1 2020
medline: 15 7 2020
entrez: 3 1 2020
Statut: ppublish

Résumé

Activated perivascular mast cells (MCs) participate in different cardiovascular diseases. Many factors provoking MC degranulation have been described, while physiological counterregulators are barely known. Endothelial CNP (C-type natriuretic peptide) participates in the maintenance of vascular barrier integrity, but the target cells and mechanisms are unclear. Here, we studied whether MCs are regulated by CNP. Approach and Results: In cultured human and murine MCs, CNP activated its specific GC (guanylyl cyclase)-B receptor and cyclic GMP signaling. This enhanced cyclic GMP-dependent phosphorylation of the cytoskeleton-associated VASP (vasodilator-stimulated phosphoprotein) and inhibited ATP-evoked degranulation. To elucidate the relevance in vivo, mice with a floxed GC-B ( CNP, via GC-B/cyclic GMP signaling, stabilizes resident perivascular MCs at baseline and prevents their excessive activation under pathological conditions. Thereby CNP contributes to the maintenance of vascular integrity in physiology and disease.

Identifiants

pubmed: 31893950
doi: 10.1161/ATVBAHA.119.313702
doi:

Substances chimiques

Cell Adhesion Molecules 0
Microfilament Proteins 0
Phosphoproteins 0
vasodilator-stimulated phosphoprotein 0
Natriuretic Peptide, C-Type 127869-51-6
Adenosine Triphosphate 8L70Q75FXE
Receptors, Atrial Natriuretic Factor EC 4.6.1.2
atrial natriuretic factor receptor B EC 4.6.1.2
Cyclic GMP H2D2X058MU

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

682-696

Auteurs

Wen Chen (W)

From the Institute of Physiology, University of Würzburg, Germany (W.C., F.W., K.V., T.P., M.K.).
Comprehensive Heart Failure Center (W.C., U.H., S.F., M.K.), University Hospital Würzburg, Germany.

Franziska Werner (F)

From the Institute of Physiology, University of Würzburg, Germany (W.C., F.W., K.V., T.P., M.K.).

Anja Illerhaus (A)

Institute of Experimental Biomedicine (M.R., A.Z.), University Hospital Würzburg, Germany.

Tanja Knopp (T)

Department of Dermatology, University of Cologne, Germany (A.I.).

Katharina Völker (K)

From the Institute of Physiology, University of Würzburg, Germany (W.C., F.W., K.V., T.P., M.K.).

Tamara Potapenko (T)

From the Institute of Physiology, University of Würzburg, Germany (W.C., F.W., K.V., T.P., M.K.).

Ulrich Hofmann (U)

Comprehensive Heart Failure Center (W.C., U.H., S.F., M.K.), University Hospital Würzburg, Germany.

Stefan Frantz (S)

Comprehensive Heart Failure Center (W.C., U.H., S.F., M.K.), University Hospital Würzburg, Germany.

Hideo A Baba (HA)

Center of Thrombosis and Hemostasis, University Medical Center of the Johannes Gutenberg-University Mainz, Germany (T.K., S.K., P.W.).

Melanie Rösch (M)

Institute of Experimental Biomedicine (M.R., A.Z.), University Hospital Würzburg, Germany.

Alma Zernecke (A)

Institute of Experimental Biomedicine (M.R., A.Z.), University Hospital Würzburg, Germany.

Susanne Karbach (S)

Department of Dermatology, University of Cologne, Germany (A.I.).
Institute of Pathology, University Hospital Essen, University Duisburg-Essen (H.A.B.).

Philip Wenzel (P)

Department of Dermatology, University of Cologne, Germany (A.I.).
Institute of Pathology, University Hospital Essen, University Duisburg-Essen (H.A.B.).

Michaela Kuhn (M)

From the Institute of Physiology, University of Würzburg, Germany (W.C., F.W., K.V., T.P., M.K.).
Comprehensive Heart Failure Center (W.C., U.H., S.F., M.K.), University Hospital Würzburg, Germany.

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Classifications MeSH