Stabilization of Perivascular Mast Cells by Endothelial CNP (C-Type Natriuretic Peptide).
Adenosine Triphosphate
/ metabolism
Animals
Capillary Permeability
Cell Adhesion Molecules
/ metabolism
Cell Degranulation
/ drug effects
Cell Line
Cyclic GMP
/ metabolism
Disease Models, Animal
Endothelial Cells
/ drug effects
Mast Cells
/ drug effects
Mice, 129 Strain
Mice, Inbred C57BL
Mice, Knockout
Microfilament Proteins
/ metabolism
Myocardial Reperfusion Injury
/ genetics
Natriuretic Peptide, C-Type
/ metabolism
Neutrophil Infiltration
Paracrine Communication
Phosphoproteins
/ metabolism
Phosphorylation
Receptors, Atrial Natriuretic Factor
/ agonists
Signal Transduction
Thrombosis
/ genetics
cyclic GMP
guanyllyl cyclase
mast cells
microcirculation
natriuretic peptides
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
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