» Articles » PMID: 19148926

Interactions Between Endothelial Cells and Electrospun Methacrylic Terpolymer Fibers for Engineered Vascular Replacements

Overview
Date 2009 Jan 17
PMID 19148926
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

A compliant terpolymer made of hexylmethacrylate (HMA), methylmethacrylate (MMA), and methacrylic acid (MAA) intended for use in small diameter vascular graft applications has been developed. The mechanical properties and in vitro biostability of this terpolymer have been previously characterized. The goal of this investigation was to examine the interactions between endothelial cells and the new terpolymer and to evaluate endothelial cell function. Electrospinning was used to produce both oriented and random terpolymer fiber scaffolds. Smooth solution cast films and tissue culture polystyrene were used as negative and positive controls, respectively. Human blood outgrowth endothelial cells and human umbilical vein endothelial cells were incubated with the test and control samples and characterized with respect to initial cell attachment, proliferation, viability, and maintenance of the endothelial cell phenotype. It was found that the terpolymer is cytocompatible allowing endothelial cell growth, with random fibers being more effective in promoting enhanced cellular activities than oriented fibers. In addition, endothelial cells cultured on these substrates appeared to maintain their phenotype. The results from this study demonstrate that electrospun HMA:MMA:MAA terpolymer has the potential to be used successfully in fabricating small diameter blood vessel replacements.

Citing Articles

The influence of physical and spatial substrate characteristics on endothelial cells.

Bjorgvinsdottir O, Ferguson S, Snorradottir B, Gudjonsson T, Wuertz-Kozak K Mater Today Bio. 2024; 26:101060.

PMID: 38711934 PMC: 11070711. DOI: 10.1016/j.mtbio.2024.101060.


Development of Silk Fibroin Scaffolds for Vascular Repair.

Duran-Rey D, Brito-Pereira R, Ribeiro C, Ribeiro S, Sanchez-Margallo J, Crisostomo V Biomacromolecules. 2023; 24(3):1121-1130.

PMID: 36754364 PMC: 10016106. DOI: 10.1021/acs.biomac.2c01124.


Development and evaluation of different electroactive poly(vinylidene fluoride) architectures for endothelial cell culture.

Duran-Rey D, Brito-Pereira R, Ribeiro C, Ribeiro S, Sanchez-Margallo J, Crisostomo V Front Bioeng Biotechnol. 2022; 10:1044667.

PMID: 36338140 PMC: 9626752. DOI: 10.3389/fbioe.2022.1044667.


Media-based effects on the hydrolytic degradation and crystallization of electrospun synthetic-biologic blends.

Nelson M, Johnson J, Lannutti J J Mater Sci Mater Med. 2013; 25(2):297-309.

PMID: 24178985 DOI: 10.1007/s10856-013-5077-0.


Endothelial outgrowth cells: function and performance in vascular grafts.

Glynn J, Hinds M Tissue Eng Part B Rev. 2013; 20(4):294-303.

PMID: 24004404 PMC: 4123462. DOI: 10.1089/ten.TEB.2013.0285.


References
1.
Wilson C, Clegg R, Leavesley D, Pearcy M . Mediation of biomaterial-cell interactions by adsorbed proteins: a review. Tissue Eng. 2005; 11(1-2):1-18. DOI: 10.1089/ten.2005.11.1. View

2.
Veleva A, Cooper S, Patterson C . Selection and initial characterization of novel peptide ligands that bind specifically to human blood outgrowth endothelial cells. Biotechnol Bioeng. 2007; 98(1):306-12. DOI: 10.1002/bit.21420. View

3.
Lin Y, Weisdorf D, Solovey A, Hebbel R . Origins of circulating endothelial cells and endothelial outgrowth from blood. J Clin Invest. 2000; 105(1):71-7. PMC: 382587. DOI: 10.1172/JCI8071. View

4.
Lin H, Sun W, Mosher D, Garcia-Echeverria C, Schaufelberger K, Lelkes P . Synthesis, surface, and cell-adhesion properties of polyurethanes containing covalently grafted RGD-peptides. J Biomed Mater Res. 1994; 28(3):329-42. DOI: 10.1002/jbm.820280307. View

5.
Inoguchi H, Tanaka T, Maehara Y, Matsuda T . The effect of gradually graded shear stress on the morphological integrity of a huvec-seeded compliant small-diameter vascular graft. Biomaterials. 2006; 28(3):486-95. DOI: 10.1016/j.biomaterials.2006.09.020. View