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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Published inScience and technology of advanced materials Vol. 14; no. 3; pp. 35002 - 35009
Main Authors Wang, Xiupeng, He, Fupo, Li, Xia, Ito, Atsuo, Sogo, Yu, Maruyama, Osamu, Kosaka, Ryo, Ye, Jiandong
Format Journal Article
LanguageEnglish
Published United States Taylor & Francis 01.06.2013
IOP Publishing
Taylor & Francis Ltd
Taylor & Francis Group
Subjects
10.01
10.03
Adhesion
Apatite
ascorbate
Ascorbic acid
Calcium phosphates
endothelial cell
Endothelial cells
fibroblast growth factor-2
Growth factors
Magnesium
Metal plates
Nitric oxide
platelet adhesion
Surgical implants
Tissue engineering
Titanium
apatite
endothelial cell
ascorbate
10.01
fibroblast growth factor-2
10.03
platelet adhesion
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Abstract 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.
AbstractList 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.
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 inhibitedin 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.
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.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.
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.
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.
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 -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 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.
Author Maruyama, Osamu
Ye, Jiandong
Kosaka, Ryo
Wang, Xiupeng
He, Fupo
Li, Xia
Sogo, Yu
Ito, Atsuo
AuthorAffiliation 1 Human Technology Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Central 6, 1-1-1 Higashi, Tsukuba, Ibaraki 305-8566, Japan
3 School of Materials Science and Engineering, South China University of Technology, Guangzhou 510641, People’s Republic of China
2 Human Technology Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Namiki1-2-1, Tsukuba, Ibaraki 305-8564, Japan
4 National Engineering Research Center for Tissue Restoration and Reconstruction, Guangzhou 510006, People’s Republic of China
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– name: 3 School of Materials Science and Engineering, South China University of Technology, Guangzhou 510641, People’s Republic of China
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/27877575$$D View this record in MEDLINE/PubMed
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Issue 3
Keywords apatite
endothelial cell
ascorbate
10.01
fibroblast growth factor-2
10.03
platelet adhesion
Language English
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Snippet A tissue-engineered endothelial layer was prepared by culturing endothelial cells on a fibroblast growth factor-2 (FGF-2)-l-ascorbic acid phosphate magnesium...
A tissue-engineered endothelial layer was prepared by culturing endothelial cells on a fibroblast growth factor-2 (FGF-2)–l-ascorbic acid phosphate magnesium...
A tissue-engineered endothelial layer was prepared by culturing endothelial cells on a fibroblast growth factor-2 (FGF-2)– l -ascorbic acid phosphate magnesium...
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StartPage 35002
SubjectTerms 10.01
10.03
Adhesion
Apatite
ascorbate
Ascorbic acid
Calcium phosphates
endothelial cell
Endothelial cells
fibroblast growth factor-2
Growth factors
Magnesium
Metal plates
Nitric oxide
platelet adhesion
Surgical implants
Tissue engineering
Titanium
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Title Tissue-engineered endothelial cell layers on surface-modified Ti for inhibiting in vitro platelet adhesion
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Volume 14
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