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Development of Multi-layer Tubular Vascular Scaffold to Enhance Compliance by Exhibiting a Negative Poisson’s Ratio

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Abstract

Synthetic small diameter vascular grafts frequently fail owing to intimal hyperplasia, results from mismatched compliance between the vascular graft and native vessels. A vascular graft with a negative Poisson's ratio (NPR, materials expand transversely when pulled axially) was suggested to enhance compliance. We produced a three-layer tubular vascular scaffold with NRP properties. The luminal side consisted of nanosized electrospun fibers for endothelial cell (EC) growth. The middle layer was an NPR structure created using 3D printing, and the outer layer was a microsized electrospun fiber layer for vascular smooth muscle cell (VSMC) growth. The developed multi-layer tubular vascular scaffold contained NPR value. And the NPR vascular scaffold showed 1.7 time higher compliance than the PPR scaffold and 3.8 times higher than that of commercial polytetrafluoroethylene (PTFE) vascular graft. In addition, the ECs and VSMCs were well survived and proliferated on the scaffold during 10 days of culture. From the optimized co-culture condition of the VSMCs and ECs that VSMC phenotype changed was inhibited, we successfully generated a thin luminal layer, which consisted of ECs and the proper thickness of the VSMC layer under the ECs. This scaffold may have a potential to replace conventional artificial vascular graft by providing enhanced compliance and improved cell culture environment.

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References

  1. Hasan, A., et al. (2014). Electrospun scaffolds for tissue engineering of vascular grafts. Acta Biomaterialia, 10(1), 11–25.

    Article  Google Scholar 

  2. Greenwald, S. E., & Berry, C. L. (2000). Improving vascular grafts: the importance of mechanical and haemodynamic properties. The Journal of Pathology, 190(3), 292–299.

    Article  Google Scholar 

  3. Fozdar, D. Y., et al. (2011). Three-dimensional polymer constructs exhibiting a tunable negative Poisson’s ratio. Advanced Functional Materials, 21, 2712–2720.

    Article  Google Scholar 

  4. Kurane, A., Simionescu, D., & Vyavahare, N. (2007). In vivo cellular repopulation of tubular elastin scaffolds mediated by basic fibroblast growth factor. Biomaterials, 28, 2830–2838.

    Article  Google Scholar 

  5. Conte, M. S. (1998). The ideal small arterial substitute: a search for the Holy Grail. FASEB Journal, 12, 43–45.

    Article  Google Scholar 

  6. Popov, E. P. (1990). Engineering mechanics of solid (1st ed., pp. 82–83). Prentice Hall.

    Google Scholar 

  7. Evans, K. E., et al. (1991). Molecular network design. Nature, 353, 124–124.

    Article  Google Scholar 

  8. Grima, J. N., & Gatt, R. (2010). Perforated sheets exhibiting negative Poisson’s ratios. Advanced Engineering Materials, 12, 460–464.

    Article  Google Scholar 

  9. Singh, C., Wong, C. S., & Wang, X. (2015). Medical textiles as vascular implants and their success to mimic natural arteries. Journal of Functional Biomaterials, 6(3), 500–525.

    Article  Google Scholar 

  10. Dora, K. A. (2001). Cell–cell communication in the vessel wall. Vascular Medicine, 6, 43–50.

    Article  Google Scholar 

  11. Heydarkhan-Hagvall, S., et al. (2003). Co-culture of endothelial cells and smooth muscle cells affects gene expression of angiogenic factors. Journal of Cellular Biochemistry, 89(6), 1250–1259.

    Article  Google Scholar 

  12. Korff, T., et al. (2001). Blood vessel maturation in a 3-dimensional spheroidal coculture model: direct contact with smooth muscle cells regulates endothelial cell quiescence and abrogates VEGF responsiveness. FASEB Journal, 15(2), 447–457.

    Article  Google Scholar 

  13. Ahn, H., et al. (2015). Engineered small diameter vascular grafts by combining cell sheet engineering and electrospinning technology. Acta Biomaterialia, 16, 14–22.

    Article  Google Scholar 

  14. Gaspar, N., et al. (2005). Novel honeycombs with auxetic behavior. Acta Materialia, 53, 2439–2445.

    Article  Google Scholar 

  15. Smith, C. W., Grima, J. N., & Evans, K. E. (2000). A novel mechanism for generating auxetic behaviour in reticulated foams: missing rib foam model. Acta Materialia, 48, 4349–4356.

    Article  Google Scholar 

  16. Walden, R., et al. (1980). Matched elastic properties and successful arterial grafting. Archives of Surgery, 115(10), 1166–1169.

    Article  Google Scholar 

  17. Rensen, S. S., Doevendans, P. A., & van Eys, G. J. (2007). Regulation and characteristics of vascular smooth muscle cell phenotypic diversity. Netherlands Heart Journal, 15(3), 100–108.

    Article  Google Scholar 

  18. Pusztaszeri, M. P., Seelentag, W., & Bosman, F. T. (2006). Immunohistochemical expression of endothelial markers CD31, CD34, von Willebrand factor, and Fli-1 in normal human tissues. Journal of Histochemistry & Cytochemistry, 54, 385–395.

    Article  Google Scholar 

  19. Ercolani, E., Gaudio, C. D., & Bianco, A. (2015). Vascular tissue engineering of small-diameter blood vessels: reviewing the electrospinning approach. Journal of Tissue Engineering and Regenerative Medicine, 9, 861–888.

    Article  Google Scholar 

  20. Pu, J., et al. (2015). Electrospun bilayer fibrous scaffolds for enhanced cell infiltration and vascularization in vivo. Acta Biomaterialia, 13, 131–141.

    Article  Google Scholar 

  21. Xu, C. Y., et al. (2004). Aligned biodegradable nanofibrous structure: a potential scaffold for blood vessel engineering. Biomaterials, 25, 877–886.

    Article  Google Scholar 

  22. Gooch, K. J., et al. (2018). Biomechanics and mechanobiology of saphenous vein grafts. Journal of Biomechanical Engineering, 140, 020804.

    Article  Google Scholar 

  23. Ye, L., et al. (2015). The fabrication of double layer tubular vascular tissue engineering scaffold via coaxial electrospinning and its 3D cell coculture. Journal of Biomedical Materials Research Part A, 103, 3863–3871.

    Article  Google Scholar 

  24. Ju, Y. M., et al. (2010). Bilayered scaffold for engineering cellularized blood vessels. Biomaterials, 31, 4313–4321.

    Article  Google Scholar 

  25. Ozolanta, I., et al. (1998). Changes in themechanical properties, biochemical contents and wall structure of the human coronary arteries with age and sex. Medical Engineering & Physics, 20, 523–533.

    Article  Google Scholar 

  26. Xiang, W., et al. (2017). Co-cultures of endothelial cells and smooth muscle cells affect vascular calcification. International Journal of Clinical and Experimental Medicine, 10(6), 9038–9046.

    Google Scholar 

  27. Williams, C., & Wick, T. M. (2005). Endothelial cell-smooth muscle cell co-culture in a perfusion bioreactor system. Annals of Biomedical Engineering, 33, 920–928.

    Article  Google Scholar 

  28. Davies, P. F. (1986). Vascular cell interactions with special reference to the pathogenesis of atherosclerosis. Laboratory Investigation, 55, 5–24.

    Google Scholar 

  29. Davies, P. F., et al. (1988). Endothelial communication. State of the art lecture. Hypertension, 11, 563–572.

    Google Scholar 

  30. Chan-Park, M. B., et al. (2009). Biomimetic control of vascular smooth muscle cell morphology and phenotype for functional tissue engineered small-diameter blood vessels. Journal of Biomedical Materials Research Part A, 88, 1104–1121.

    Article  Google Scholar 

  31. Vatankhaha, E., Prabhakaranb, M. P., & Ramakrishnab, S. (2017). Impact of electrospun Tecophilic/gelatin scaffold biofunctionalization on proliferation of vascular smooth muscle cells. Scientia Iranica, 24(6), 3458–3465.

    Google Scholar 

  32. Madden, L. R., et al. (2010). Proangiogenic scaffolds as functional templates for cardiac tissue engineering. Proceedings of the National Academy of Science of the United States of America, 107(34), 15211–15216.

    Article  Google Scholar 

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Acknowledgements

This research was supported by the National Research Foundation of Korea (NRF) (2020R1A2C200652811) and the Gachon University research fund of 2018 (GCU-2018-0367).

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C.B.A., J.H.K., K.H.S., and J.W.L conceived the experiments, C.B.A., J.H.K., J.-H.L conducted the experiments, K.Y.P., K.H.L., and J.W.L. analyzed the results. K.H.S. and J.W.L. wrote the article. All authors reviewed the manuscript.

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Correspondence to Kuk Hui Son or Jin Woo Lee.

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Ahn, C.B., Kim, J.H., Lee, JH. et al. Development of Multi-layer Tubular Vascular Scaffold to Enhance Compliance by Exhibiting a Negative Poisson’s Ratio. Int. J. of Precis. Eng. and Manuf.-Green Tech. 8, 841–853 (2021). https://doi.org/10.1007/s40684-021-00332-9

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