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Tissue-engineered endothelial cell layers on surface-modified Ti for inhibiting in vitro platelet adhesion

A tissue-engineered endothelial layer was prepared by culturing endothelial cells on a fibroblast growth factor-2 (FGF-2)–l-ascorbic acid phosphate magnesium salt n-hydrate (AsMg)–apatite (Ap) coated titanium plate. The FGF-2–AsMg–Ap coated Ti plate was prepared by immersing a Ti plate in supersatur...

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Detalles Bibliográficos
Autores principales: Wang, Xiupeng, He, Fupo, Li, Xia, Ito, Atsuo, Sogo, Yu, Maruyama, Osamu, Kosaka, Ryo, Ye, Jiandong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5090506/
https://www.ncbi.nlm.nih.gov/pubmed/27877575
http://dx.doi.org/10.1088/1468-6996/14/3/035002
Descripción
Sumario:A tissue-engineered endothelial layer was prepared by culturing endothelial cells on a fibroblast growth factor-2 (FGF-2)–l-ascorbic acid phosphate magnesium salt n-hydrate (AsMg)–apatite (Ap) coated titanium plate. The FGF-2–AsMg–Ap coated Ti plate was prepared by immersing a Ti plate in supersaturated calcium phosphate solutions supplemented with FGF-2 and AsMg. The FGF-2–AsMg–Ap layer on the Ti plate accelerated proliferation of human umbilical vein endothelial cells (HUVECs), and showed slightly higher, but not statistically significant, nitric oxide release from HUVECs than on as-prepared Ti. The endothelial layer maintained proper function of the endothelial cells and markedly inhibited in vitro platelet adhesion. The tissue-engineered endothelial layer formed on the FGF-2–AsMg–Ap layer is promising for ameliorating platelet activation and thrombus formation on cardiovascular implants.