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http://purl.uniprot.org/citations/23154239http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/23154239http://www.w3.org/2000/01/rdf-schema#comment"

Aims

Endothelial cells play a pivotal role in vascular intimal inflammation during cardiovascular diseases. The chemerin/ChemR23 system in endothelial cells is one of physiological mechanisms that regulate inflammatory responses. Our previous studies indicated that stimulation of non-neuronal muscarinic receptor (NNMR) improved endothelial dysfunction. However, the relationship between the chemerin/ChemR23 signaling axis and NNMR in endothelial cell is poorly understood. Here, we first investigated whether the modulation of chemerin/ChemR23 signaling axis is involved in NNMR-mediated endothelial protection.

Main methods

Cultured rat aortic endothelial cells (RAECs) were used. The ChemR23 protein expression and chemerin secretion were measured using Western blot analysis. The gene expression level of ChemR23 was examined with reverse transcriptase PCR (RT-PCR). The production of nitric oxide (NO) was determined by a nitrate reductase assay kit.

Key findings

A sharp decline of chemerin secretion and ChemR23 protein/gene expression was observed in RAECs after exposed to homocysteine at concentration of 0.5 mmol/L. Arecoline (10 μmol/L) pretreatment increased ChemR23 protein expression as well as mRNA expression, and enhanced the secretion of chemerin. Arecoline could also reverse the decreased ChemR23 mRNA expression induced by uric acid, high glucose, or oxidized low-density lipoprotein. Furthermore, the modulation of arecoline on chemerin/ChemR23 signaling axis was absolutely abolished in the presence of the nonselective muscarinic receptors antagonist atropine 1 μmol/L. Additionally, arecoline improved endothelial dysfunction by increasing the reduced NO production induced by uric acid, which was blocked by anti-ChemR23 antibody.

Significance

The chemerin/ChemR23 signaling axis participates in NNMR-mediated protection against endothelial dysfunction in cardiovascular system."xsd:string
http://purl.uniprot.org/citations/23154239http://purl.org/dc/terms/identifier"doi:10.1016/j.lfs.2012.10.029"xsd:string
http://purl.uniprot.org/citations/23154239http://purl.uniprot.org/core/author"Wang H."xsd:string
http://purl.uniprot.org/citations/23154239http://purl.uniprot.org/core/author"Zhang Y.F."xsd:string
http://purl.uniprot.org/citations/23154239http://purl.uniprot.org/core/author"Pan Z.Y."xsd:string
http://purl.uniprot.org/citations/23154239http://purl.uniprot.org/core/author"Zhao R.J."xsd:string
http://purl.uniprot.org/citations/23154239http://purl.uniprot.org/core/author"Cui W.Y."xsd:string
http://purl.uniprot.org/citations/23154239http://purl.uniprot.org/core/author"Long C.L."xsd:string
http://purl.uniprot.org/citations/23154239http://purl.uniprot.org/core/date"2013"xsd:gYear
http://purl.uniprot.org/citations/23154239http://purl.uniprot.org/core/name"Life Sci"xsd:string
http://purl.uniprot.org/citations/23154239http://purl.uniprot.org/core/pages"10-16"xsd:string
http://purl.uniprot.org/citations/23154239http://purl.uniprot.org/core/title"Stimulation of non-neuronal muscarinic receptors enhances chemerin/ChemR23 system in dysfunctional endothelial cells."xsd:string
http://purl.uniprot.org/citations/23154239http://purl.uniprot.org/core/volume"92"xsd:string
http://purl.uniprot.org/citations/23154239http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/23154239
http://purl.uniprot.org/citations/23154239http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/23154239
http://purl.uniprot.org/uniprot/#_O35786-mappedCitation-23154239http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/23154239
http://purl.uniprot.org/uniprot/O35786http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/23154239