Bone Morphogenetic Protein Receptor II Is a Novel Mediator of Endothelial Nitric-oxide Synthase Activation

• Published in: The Journal of biological chemistry Vol. 286; no. 38; pp. 33134 - 33140
• Main Authors: Gangopahyay, Archana, Oran, Max, Bauer, Eileen M., Wertz, Jeffrey W., Comhair, Suzy A., Erzurum, Serpil C., Bauer, Philip M.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 23.09.2011; American Society for Biochemistry and Molecular Biology
• Subjects: Animals; BMPRII; Bone Morphogenetic Protein (BMP); Bone Morphogenetic Protein 2 - pharmacology; Bone Morphogenetic Protein 4 - pharmacology; Bone Morphogenetic Protein Receptors, Type II - metabolism; Cattle; Cell Movement - drug effects; Cyclic AMP-Dependent Protein Kinases - metabolism; Endothelial Cell; Endothelial Cells - cytology; Endothelial Cells - drug effects; Endothelial Cells - enzymology; eNOS; Enzyme Activation - drug effects; Humans; Molecular Bases of Disease; Mutation - genetics; Nitric Oxide Synthase Type III - metabolism; Nitric-oxide Synthase; Phosphorylation - drug effects; Protein Binding - drug effects; Protein Kinase A (PKA); Proto-Oncogene Proteins c-akt - metabolism; Pulmonary Artery - cytology; Pulmonary Hypertension; Bone Morphogenetic Protein (BMP); Protein Kinase A (PKA); eNOS; Nitric-oxide Synthase; Pulmonary Hypertension; Endothelial Cell; BMPRII
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M111.274100

Activation of bone morphogenetic protein (BMP) receptor II (BMPRII) promotes pulmonary artery endothelial cell (PAEC) survival, proliferation, and migration. Mutations to BMPRII are associated with the development of pulmonary arterial hypertension (PAH). Endothelial dysfunction, including decreased endothelial nitric-oxide synthase (eNOS) activity and loss of bioactive nitric oxide (NO), plays a prominent role in the development of PAH. We hypothesized that stimulation of BMPRII promotes normal PAEC function by activating eNOS. We report that BMPRII ligands, BMP2 and BMP4, (i) stimulate eNOS phosphorylation at a critical regulatory site, (ii) increase eNOS activity, and (iii) result in canonical changes in eNOS protein-protein interactions. The stimulation of eNOS activity by BMPRII ligands was largely dependent on protein kinase A (PKA) activation, as demonstrated using the PKA inhibitors H89 and myristoylated PKI(6–22) amide. PAEC migration stimulated by BMP2 and BMP4 was inhibited by the NOS inhibitor l-nitroarginine methyl ester, providing functional evidence of eNOS activation. Furthermore, BMP2 and BMP4 failed to stimulate eNOS phosphorylation when BMPRII was knocked down by siRNA. Most important to the pathophysiology of the disease, BMP2 and BMP4 failed to stimulate eNOS phosphorylation in PAECs isolated from patients with mutations in the BMPR2 gene. These data demonstrate a new action of BMPs/BMPRII in the pulmonary endothelium and provide novel mechanistic insight into the pathogenesis of PAH.