Smooth Muscle Cell Alignment and Phenotype Control by Melt Spun Polycaprolactone Fibers for Seeding of Tissue Engineered Blood Vessels
A method has been developed to induce and retain a contractile phenotype for vascular smooth muscle cells, as the first step towards the development of a biomimetic blood vessel construct with minimal compliance mismatch. Melt spun PCL fibers were deposited on a mandrel to form aligned fibers of 10 ...
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sg-ntu-dr.10356-810912023-02-28T16:56:24Z Smooth Muscle Cell Alignment and Phenotype Control by Melt Spun Polycaprolactone Fibers for Seeding of Tissue Engineered Blood Vessels Agrawal, Animesh Lee, Bae Hoon Irvine, Scott Alexander An, Jia Bhuthalingam, Ramya Singh, Vaishali Low, Kok Yao Chua, Chee Kai Venkatraman, Subbu Subramanian School of Materials Science & Engineering School of Mechanical and Aerospace Engineering School of Biological Sciences A method has been developed to induce and retain a contractile phenotype for vascular smooth muscle cells, as the first step towards the development of a biomimetic blood vessel construct with minimal compliance mismatch. Melt spun PCL fibers were deposited on a mandrel to form aligned fibers of 10 μm in diameter. The fibers were bonded into aligned arrangement through dip coating in chitosan solution. This formed a surface of parallel grooves, 10 μm deep by 10 μm across, presenting a surface layer of chitosan to promote cell surface interactions. The aligned fiber surface was used to culture cells present in the vascular wall, in particular fibroblasts and smooth muscle cells. This topography induced “surface guidance” over the orientation of the cells, which adopted an elongated spindle-like morphology, whereas cells on the unpatterned control surface did not show such orientation, assuming more rhomboid shapes. The preservation of VSMC contractile phenotype on the aligned scaffold was demonstrated by the retention of α-SMA expression after several days of culture. The effect was assessed on a prototype vascular graft prosthesis fabricated from polylactide caprolactone; VSMCs aligned longitudinally along a fiberless tube, whereas, for the aligned fiber coated tubes, the VSMCs aligned in the required circumferential orientation. NRF (Natl Research Foundation, S’pore) ASTAR (Agency for Sci., Tech. and Research, S’pore) Published version 2015-12-14T02:49:16Z 2019-12-06T14:21:12Z 2015-12-14T02:49:16Z 2019-12-06T14:21:12Z 2015 Journal Article Agrawal, A., Lee, B. H., Irvine, S. A., An, J., Bhuthalingam, R., Singh, V., et al. (2015). Smooth Muscle Cell Alignment and Phenotype Control by Melt Spun Polycaprolactone Fibers for Seeding of Tissue Engineered Blood Vessels. International Journal of Biomaterials, 2015, 434876-. 1687-8787 https://hdl.handle.net/10356/81091 http://hdl.handle.net/10220/39072 10.1155/2015/434876 26413093 en International Journal of Biomaterials © 2015 Animesh Agrawal et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. 8 p. application/pdf |
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A method has been developed to induce and retain a contractile phenotype for vascular smooth muscle cells, as the first step towards the development of a biomimetic blood vessel construct with minimal compliance mismatch. Melt spun PCL fibers were deposited on a mandrel to form aligned fibers of 10 μm in diameter. The fibers were bonded into aligned arrangement through dip coating in chitosan solution. This formed a surface of parallel grooves, 10 μm deep by 10 μm across, presenting a surface layer of chitosan to promote cell surface interactions. The aligned fiber surface was used to culture cells present in the vascular wall, in particular fibroblasts and smooth muscle cells. This topography induced “surface guidance” over the orientation of the cells, which adopted an elongated spindle-like morphology, whereas cells on the unpatterned control surface did not show such orientation, assuming more rhomboid shapes. The preservation of VSMC contractile phenotype on the aligned scaffold was demonstrated by the retention of α-SMA expression after several days of culture. The effect was assessed on a prototype vascular graft prosthesis fabricated from polylactide caprolactone; VSMCs aligned longitudinally along a fiberless tube, whereas, for the aligned fiber coated tubes, the VSMCs aligned in the required circumferential orientation. |
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School of Materials Science & Engineering |
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School of Materials Science & Engineering Agrawal, Animesh Lee, Bae Hoon Irvine, Scott Alexander An, Jia Bhuthalingam, Ramya Singh, Vaishali Low, Kok Yao Chua, Chee Kai Venkatraman, Subbu Subramanian |
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Article |
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Agrawal, Animesh Lee, Bae Hoon Irvine, Scott Alexander An, Jia Bhuthalingam, Ramya Singh, Vaishali Low, Kok Yao Chua, Chee Kai Venkatraman, Subbu Subramanian |
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Agrawal, Animesh Lee, Bae Hoon Irvine, Scott Alexander An, Jia Bhuthalingam, Ramya Singh, Vaishali Low, Kok Yao Chua, Chee Kai Venkatraman, Subbu Subramanian Smooth Muscle Cell Alignment and Phenotype Control by Melt Spun Polycaprolactone Fibers for Seeding of Tissue Engineered Blood Vessels |
author_sort |
Agrawal, Animesh |
title |
Smooth Muscle Cell Alignment and Phenotype Control by Melt Spun Polycaprolactone Fibers for Seeding of Tissue Engineered Blood Vessels |
title_short |
Smooth Muscle Cell Alignment and Phenotype Control by Melt Spun Polycaprolactone Fibers for Seeding of Tissue Engineered Blood Vessels |
title_full |
Smooth Muscle Cell Alignment and Phenotype Control by Melt Spun Polycaprolactone Fibers for Seeding of Tissue Engineered Blood Vessels |
title_fullStr |
Smooth Muscle Cell Alignment and Phenotype Control by Melt Spun Polycaprolactone Fibers for Seeding of Tissue Engineered Blood Vessels |
title_full_unstemmed |
Smooth Muscle Cell Alignment and Phenotype Control by Melt Spun Polycaprolactone Fibers for Seeding of Tissue Engineered Blood Vessels |
title_sort |
smooth muscle cell alignment and phenotype control by melt spun polycaprolactone fibers for seeding of tissue engineered blood vessels |
publishDate |
2015 |
url |
https://hdl.handle.net/10356/81091 http://hdl.handle.net/10220/39072 |
_version_ |
1759853445671550976 |