Journal
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
Volume 321, Issue 6, Pages H1083-H1095Publisher
AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpheart.00065.2021
Keywords
leukocyte adhesion; nitric oxide; protein kinase; S-nitrosylation
Funding
- Vicerrectoria de Investigacion, Desarrollo y Creacion Artistica (VIDCA)-Universidad Austral de Chile (UACh) Grant 2020
- National Fund for Scientific and Technological Development (FONDECYT) Grant [1201635]
- FONDECYT National Commission for Scientific and Technological Research (CONICYT) Grant [PFB12/2007]
- Programa de Apoyo a Centros con Financiamiento Basal Grant [AFB 170005]
- National Institutes of Health (NIH) [R56HL134842-01, R01HL146539, HL087823, NIH GM122940]
- NIH [NS046593, 1S10OD025047-01]
- (UMFLUCEL) Fondequip, Instituto de Fisiologia, Facultad de Medicina, UACh [EQM 1501118]
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Nitric oxide, produced by eNOS, promotes leukocyte adhesion through the S-nitrosylation pathway, contrary to its known inhibitory role, potentially involving PKCf S-nitrosylation as a key regulatory step.
Nitric oxide ( NO) is a key factor in inflammation. Endothelial nitric oxide synthase (eNOS), whose activity increases after stimulation with proinflammatory cytokines, produces NO in endothelium. NO activates two pathways: 1) soluble guanylate cyclase-protein kinase G and 2) S-nitrosylation (NO-induced modification of free-thiol cysteines in proteins). S-nitrosylation affects phosphorylation, localization, and protein interactions. NO is classically described as a negative regulator of leukocyte adhesion to endothelial cells. However, agonists activating NO production induce a fast leukocyte adhesion, which suggests that NO might positively regulate leukocyte adhesion. We tested the hypothesis that eNOS-induced NO promotes leukocyte adhesion through the S-nitrosylation pathway. We stimulated leukocyte adhesion to endothelium in vitro and in vivo using tumor necrosis factor-alpha (TNF-alpha) as proinflammatory agonist. ICAM-1 changes were evaluated by immunofluorescence, subcellular fractionation, immunoprecipitation, and fluorescence recovery after photobleaching (FRAP). Protein kinase C sigma (PKC sigma) activity and S-nitrosylation were evaluated by Western blot analysis and biotin switch method, respectively. TNF-alpha, at short times of stimulation, activated the eNOS S-nitrosylation pathway and caused leukocyte adhesion to endothelial cells in vivo and in vitro. TNF-alpha-induced NO led to changes in ICAM-1 at the cell surface, which are characteristic of clustering. TNF-alpha-induced NO also produced S-nitrosylation and phosphorylation of PKCf, association of PKCf with ICAM-1, and ICAM-1 phosphorylation. The inhibition of PKCf blocked leukocyte adhesion induced by TNF-alpha. Mass spectrometry analysis of purified PKCf identified cysteine 503 as the only S-nitrosylated residue in the kinase domain of the protein. Our results reveal a new eNOS S-nitrosylation-dependent mechanism that induces leukocyte adhesion and suggests that S-nitrosylation of PKCf may be an important regulatory step in early leukocyte adhesion in inflammation. NEW & NOTEWORTHY Contrary to the well-established inhibitory role of NO in leukocyte adhesion, we demonstrate a positive role of nitric oxide in this process. We demonstrate that NO induced by eNOS after TNF-alpha treatment induces early leukocyte adhesion activating the S-nitrosylation pathway. Our data suggest that PKCf S-nitrosylation may be a key step in this process.
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