Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2015, 159(4):540-546 | DOI: 10.5507/bp.2015.009
CT-1 induces angiogenesis by regulating the ADMA/DDAH Pathway
- a Department of Cardiology, The First Afficiated Hospital of Nanchang University, Nanchang, Jiangxi, 330006, China
- b Department of Electrocardiography, Hubei Provincial Maternal and Child Health Institute, Hubei, Wuhan, 430000, China
Background: Cardiotrophin-1 (CT-1), a member of the IL-6 superfamily, is elevated in the serum of patients with ischemic and valvular heart disease. In this study, we hypothesized that CT-1 induces endothelial cell angiogenesis and that the ADMA/DDAH pathway plays an important role in the process.
Methods: pEGFP-N1-CTF1-GFP and pEGFP-N1 were constructed and used to transiently transfect to HUVECs, mediated by LipofectamineTM 2000. After transfection, the expression of CT-1 was examined by qRT-PCR and western blotting. Endothelial cell proliferation assay was evaluated using the 3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyltetrazolium bromide (MTT) method. Migration assay was performed using transwell, tube formation test was examined on Matrigel, eNOSmRNA expression was assayed by qRT-PCR, DDAH I, DDAHII and VEGF expression were detected by western blotting, the level of ADMA and the activity of DDAH were measured by High Performance Liquid Chromatography, NOS activity and the concentration of NO were assayed by L-[3H] citrulline production from L-[3H]arginine.
Results: Overexpression of CT-1, increased endothelial cell proliferation, migration and formation of blood vessels, upregulated the expression of eNOSmRNA, DDAHI, DDAHII and VEGF, elevated the activity of DDAH and NOS, decreased the level of ADMA and promoted NO synthesis. In contrast, ADMA partially inhibited the effects of CT-1 induction.
Conclusions: Overexpression of CT-1 increases cell proliferation, migration and formation of blood vessels. This result also suggests that CT-1 may regulate angiogenesis through the ADMA/DDAH pathway.
Keywords: cardiotrophin-1 (CT-1), ADMA, DDAH, eNOS, angiogenesis
Received: November 11, 2014; Accepted: February 18, 2015; Prepublished online: March 1, 2015; Published: December 3, 2015 Show citation
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