Urotensin Ⅱ promotes monocyte chemoattractant protein-1 expression in aortic adventitial fibroblasts of rat

• Published in: Chinese medical journal Vol. 127; no. 10; pp. 1907 - 1912
• Main Authors: Zhang, Yonggang, Bao, Shilin, Kuang, Zejian, Ma, Yanjun, Hu, Yanchao, Mao, Yanyan
• Format: Journal Article
• Language: English
• Published: China Department of Cardiology, Second Affiliated Hospital, Shantou University Medical College, Shantou, Guangdong 515041, China 2014; Cardiovascular Laboratory, Centre for Translational Medicine,Shantou University Medical College, Shantou, Guangdong 515041,China%Department of Cardiovascular Diseases, First Affiliated Hospital,Shantou University Medical College, Shantou, Guangdong 515041,China%Department of Cardiology, Second Affiliated Hospital, Shantou University Medical College, Shantou, Guangdong 515041, China
• Subjects: Adventitia - cytology; Animals; Aorta - cytology; Cells, Cultured; Chemokine CCL2 - genetics; Chemokine CCL2 - metabolism; Fibroblasts - drug effects; Fibroblasts - metabolism; Male; Rats; Rats, Sprague-Dawley; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger - genetics; Urotensins - pharmacology; 丝裂原活化蛋白激酶; 主动脉; 加压素; 单核细胞趋化蛋白-1; 外膜; 大鼠; 成纤维细胞; 蛋白激酶抑制剂; urotensin; monocyte chemoattractant protein-1; adventitial fibroblasts; signal transduction
• ISSN: 0366-6999; 2542-5641; 2542-5641
• DOI: 10.3760/cma.j.issn.0366-6999.20132795

Background Urotensin Ⅱ （Ull）,a potent vasoconstrictive peptide,is able to stimulate phenotypic differentiation of adventitial fibroblasts.This study aimed to determine the effect of UII on monocyte chemoattractant protein-1 （MCP1） expression in rat aortic adventitial fibroblasts,so as to explore possible mechanisms in the development of vascular inflammation.Methods Growth-arrested adventitial fibroblasts were incubated in serum-free medium with UII （1010-10-7 mol/L） and inhibitors of signal transduction pathways for 1 to 24 hours.MCP-1 mRNA and protein expression and secretion were determined by RT-PCR,Western blotting analysis and enzyme-linked immunosorbent assay （ELISA）,respectively.Results UII dose-and time-dependently promoted MCP-1 mRNA and protein expression and secretion in cells,with maximal effect at 10-8 mol/L at 3 hours for mRNA expression,24 hours for protein expression in the cells,and 12 hours for protein secretion from the cells.Furthermore,the UII effects were significantly inhibited by treatment with its receptor antagonist SB710411,Rho kinase inhibitor Y27632,protein kinase C （PKC） inhibitor H7,mitogen-activated protein kinase inhibitor PD98059,calcineurin inhibitor cyclosporine A,and the Ca2＋channel blocker nicardipine.Conclusion UII may stimulate MCP-1 expression in rat aortic adventitial fibroblasts through its receptor and Rho kinase,PKC,mitogen-activated protein kinase,calcineurin and Ca2＋ channel signal transduction,thus contributing to adventitial inflammation.