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
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