• DocumentCode
    2385811
  • Title

    Whole organ decellularization - a tool for bioscaffold fabrication and organ bioengineering

  • Author

    Baptista, Pedro M. ; Orlando, Giuseppe ; Mirmalek-Sani, Sayed-Hadi ; Siddiqui, Mohummad ; Atala, Anthony ; Soker, Shay

  • Author_Institution
    Wake Forest Inst. for Regenerative Med., Wake Forest Univ. Health Sci., Winston-Salem, NC, USA
  • fYear
    2009
  • fDate
    3-6 Sept. 2009
  • Firstpage
    6526
  • Lastpage
    6529
  • Abstract
    The use of synthetic and naturally-derived scaffolds for bioengineering of solid organs has been limited due to a lack of an integrated vascular network. Here, we describe fabrication of a bioscaffold system with intact vascular tree. Animal-donor organs and tissues, ranging in size up-to thirty centimeters, were perfused with decellularization solution to selectively remove the cellular component of the tissue and leave an intact extracellular matrix and vascular network. The vascular tree demonstrated sequential fluid flow through a central inlet vessel that branched into an extensive capillary bed and coalesced back into a single outlet vessel. In one example, the liver, we used central inlet vessels to perfuse human and animal liver cells through the bioscaffold to create a functional liver tissue construct in vitro. These results demonstrate a novel yet simple and scalable method to obtain whole organ vascularized bioscaffolds with potential for liver, kidney, pancreas, intestine and other organs´ bioengineering. These bioscaffolds can further provide a tool to study cells in their natural three-dimensional environment, which is superior for drug discovery platform compared with cells cultured in two-dimensional petri dishes.
  • Keywords
    biological fluid dynamics; blood vessels; cellular biophysics; haemorheology; liver; tissue engineering; animal donor organs; animal donor tissues; animal liver cells; bioengineering; bioscaffold system; central inlet vessel; extensive capillary bed; functional liver tissue; human liver cells; intact extracellular matrix; intact vascular tree; intestine; kidney; liver; pancreas; perfusion; sequential fluid flow; vascular network; whole organ decellularization; Animals; Bioartificial Organs; Biomedical Engineering; Cell Fractionation; Cell-Free System; Mice; Organ Culture Techniques; Tissue Engineering; Tissue Scaffolds;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Engineering in Medicine and Biology Society, 2009. EMBC 2009. Annual International Conference of the IEEE
  • Conference_Location
    Minneapolis, MN
  • ISSN
    1557-170X
  • Print_ISBN
    978-1-4244-3296-7
  • Electronic_ISBN
    1557-170X
  • Type

    conf

  • DOI
    10.1109/IEMBS.2009.5333145
  • Filename
    5333145