Skip to main content

Advertisement

Log in

Development of a Small Diameter Vascular Graft Using the Human Amniotic Membrane

  • Published:
Cardiovascular Engineering and Technology Aims and scope Submit manuscript

Abstract

Although there have been significant advances in the development of fully functional vascular grafts suitable for coronary artery bypass graft surgery, so far no technology has been developed that meets all of the requirements suitable for clinical use. Here we present an approach using a decellularized biological membrane, seeded with smooth muscle cells (SMCs) and rolled into a tubular construct. We show that the human amniotic membrane provides a thin and strong biological extracellular matrix that supports the attachment and proliferation of both rat aortic SMCs and of human myofibroblasts. The results show that after 1 week in static culture, the rolled construct develops an elastic modulus higher than that of native tissue. The elastic modulus decreases with time in culture, suggesting that cells actively remodel the matrix. Cells continue to proliferate in the rolled state and histology images show that some cells attach to the neighboring membrane in the construct. The burst pressure of the construct remains below physiological levels. A bioreactor system was used to deliver flow to both the lumen and the ablumenal spaces through two separate flow circuits but resulting burst pressures of this treatment still remain below physiological values. Our study demonstrates that the human amniotic membrane is a cell biocompatible biological membrane that has the potential to be useful in a vascular application.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Figure 1
Figure 2
Figure 3
Figure 4
Figure 5
Figure 6
Figure 7
Figure 8
Figure 9

Similar content being viewed by others

References

  1. Alford, P. W., et al. Vascular smooth muscle contractility depends on cell shape. Integr. Biol. 3(11):1063–1070, 2011.

    Article  Google Scholar 

  2. Amensag, S., and P. S. McFetridge. Rolling the human amnion to engineer laminated vascular tissues. Tissue Eng Part C Methods 18(11):903–912, 2012.

    Article  Google Scholar 

  3. Amiel, G. E., et al. Engineering of blood vessels from acellular collagen matrices coated with human endothelial cells. Tissue Eng. 12(8):2355–2365, 2006.

    Article  Google Scholar 

  4. Arrigoni, C., et al. The effect of sodium ascorbate on the mechanical properties of hyaluronan-based vascular constructs. Biomaterials 27(4):623–630, 2006.

    Article  Google Scholar 

  5. Beamish, J. A., et al. Molecular regulation of contractile smooth muscle cell phenotype: implications for vascular tissue engineering. Tissue Eng. Part B 16(5):467–491, 2010.

    Article  Google Scholar 

  6. Bilodeau, K., et al. Design of a perfusion bioreactor specific to the regeneration of vascular tissues under mechanical stresses. Artif. Organs 29(11):906–912, 2005.

    Article  Google Scholar 

  7. Campbell, G. R., and J. H. Campbell. Development of tissue engineered vascular grafts. Curr. Pharm. Biotechnol. 8(1):43–50, 2007.

    Article  Google Scholar 

  8. Chlupac, J., E. Filova, and L. Bacakova. Blood vessel replacement: 50 years of development and tissue engineering paradigms in vascular surgery. Physiol. Res. 58(Suppl 2):S119–S139, 2009.

    Google Scholar 

  9. Crapo, P. M., T. W. Gilbert, and S. F. Badylak. An overview of tissue and whole organ decellularization processes. Biomaterials 32(12):3233–3243, 2011.

    Article  Google Scholar 

  10. Dahan, N., et al. Porcine small diameter arterial extracellular matrix supports endothelium formation and media remodeling forming a promising vascular engineered biograft. Tissue Eng. Part A 18(3–4):411–422, 2012.

    Article  Google Scholar 

  11. Forsey, R. W., and J. B. Chaudhuri. Validity of DNA analysis to determine cell numbers in tissue engineering scaffolds. Biotechnol. Lett. 31(6):819–823, 2009.

    Article  Google Scholar 

  12. Gilbert, T. W., T. L. Sellaro, and S. F. Badylak. Decellularization of tissues and organs. Biomaterials 27(19):3675–3683, 2006.

    Google Scholar 

  13. Girton, T. S., et al. Mechanisms of stiffening and strengthening in media-equivalents fabricated using glycation. Trans. ASME 122:7, 2001.

    Google Scholar 

  14. Gui, L. Q., et al. Development of decellularized human umbilical arteries as small-diameter vascular grafts. Tissue Eng. Part A 15(9):2665–2676, 2009.

    Article  Google Scholar 

  15. Hopkinson, A., et al. Amniotic membrane for ocular surface reconstruction: donor variations and the effect of handling on TGF-beta content. Invest. Ophthalmol. Vis. Sci. 47(10):4316–4322, 2006.

    Article  Google Scholar 

  16. Isenberg, B. C., C. Williams, and R. T. Tranquillo. Small-diameter artificial arteries engineered in vitro. Circ. Res. 98(1):25–35, 2006.

    Article  Google Scholar 

  17. Iwasaki, K., et al. Bioengineered three-layered robust and elastic artery using hemodynamically-equivalent pulsatile bioreactor. Circulation 118(14):S52–S57, 2008.

    Article  Google Scholar 

  18. Konig, G., et al. Mechanical properties of completely autologous human tissue engineered blood vessels compared to human saphenous vein and mammary artery. Biomaterials 30(8):1542–1550, 2009.

    Article  Google Scholar 

  19. Lee, P. H., et al. A prototype tissue engineered blood vessel using amniotic membrane as scaffold. Acta Biomater. 8(9):3342–3348, 2012.

    Article  Google Scholar 

  20. L’Heureux, N., et al. A completely biological tissue-engineered human blood vessel. FASEB J. 12(1):47–56, 1998.

    Google Scholar 

  21. Liu, G. F., et al. Decellularized aorta of fetal pigs as a potential scaffold for small diameter tissue engineered vascular graft. Chin. Med. J. (Engl.) 121(15):1398–1406, 2008.

    Google Scholar 

  22. Luo, J. C., et al. A multi-step method for preparation of porcine small intestinal submucosa (SIS). Biomaterials 32(3):706–713, 2011.

    Article  Google Scholar 

  23. Maharajan, V. S., et al. Amniotic membrane transplantation for ocular surface reconstruction: indications and outcomes. Clin. Exp. Ophthalmol. 35(2):140–147, 2007.

    Google Scholar 

  24. McFetridge, P. S., et al. Preparation of porcine carotid arteries for vascular tissue engineering applications. J. Biomed. Mater. Res. A 70(2):224–234, 2004.

    Article  Google Scholar 

  25. Niklason, L. E., et al. Functional arteries grown in vitro. Science 284(5413):489–493, 1999.

    Article  Google Scholar 

  26. Powell, D. W., et al. Myofibroblasts. I. Paracrine cells important in health and disease. Am. J. Physiol. 277(1 Pt 1):C1–C9, 1999.

    Article  Google Scholar 

  27. Rayatpisheh, S., et al. Aligned 3D human aortic smooth muscle tissue via layer by layer technique inside microchannels with novel combination of collagen and oxidized alginate hydrogel. J. Biomed. Mater. Res. A 98(2):235–244, 2011.

    Article  Google Scholar 

  28. Reing, J. E., et al. The effects of processing methods upon mechanical and biologic properties of porcine dermal extracellular matrix scaffolds. Biomaterials 31(33):8626–8633, 2010.

    Article  Google Scholar 

  29. Rosenberg, N., et al. The modified bovine arterial graft. Arch. Surg. 111(3):222–226, 1976.

    Article  Google Scholar 

  30. Seliktar, D., et al. Dynamic mechanical conditioning of collagen-gel blood vessel constructs induces remodeling in vitro. Ann. Biomed. Eng. 28(4):351–362, 2000.

    Article  Google Scholar 

  31. Tosi, G. M., et al. Amniotic membrane transplantation in ocular surface disorders. J. Cell. Physiol. 202(3):849–851, 2005.

    Article  Google Scholar 

  32. Vunjak-Novakovic, G., and R. I. Freshney. Culture of Cells for Tissue Engineering. Hoboken, NJ: Wiley-Liss, 2006, xiii, 512 pp.

  33. Weinberg, C. B., and E. Bell. A blood vessel model constructed from collagen and cultured vascular cells. Science 231(4736):397–400, 1986.

    Article  Google Scholar 

  34. Wilshaw, S. P., et al. Production of an acellular amniotic membrane matrix for use in tissue engineering. Tissue Eng. 12(8):2117–2129, 2006.

    Article  Google Scholar 

Download references

Acknowledgments

The authors would like to thank Dr. Eric Howard’s laboratory from the University of Oklahoma Health Sciences Center for kindly donating the SMCs as well as Normal Regional Hospital for providing the placentas to make our research possible. This work was funded by the American Heart Association.

Conflict of interest

Authors Brennan, Arrizabalaga, and Nollert declare that they have no conflict of interest.

Ethical Standards

All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration of 1975, as revised in 2000 (5). Informed consent was obtained from all patients for being included in the study.

Animal Studies

No animal studies were carried out by the authors for this article.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Matthias U. Nollert.

Additional information

Associate Editor Ajit P. Yoganathan oversaw the review of this article.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Brennan, J.A., Arrizabalaga, J.H. & Nollert, M.U. Development of a Small Diameter Vascular Graft Using the Human Amniotic Membrane. Cardiovasc Eng Tech 5, 96–109 (2014). https://doi.org/10.1007/s13239-013-0170-6

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s13239-013-0170-6

Keywords

Navigation