Hostname: page-component-848d4c4894-xfwgj Total loading time: 0 Render date: 2024-06-24T22:07:37.843Z Has data issue: false hasContentIssue false

Soft-Tissue Analogue Design and Tissue Engineering of Liver

Published online by Cambridge University Press:  29 November 2013

Get access

Extract

Tissue engineering involves the application of physical and life sciences to develop functional substitutes for dysfunctional organs or tissue structures. From an engineering standpoint, tissues contain two basic components—the cells that are organized into proper units, and the material surrounding the cells, called the extracellular matrix (ECM). A third, frequently overlooked feature essential to the maintenance of the activity of the engineered tissue is the three-dimensional architecture of the cell-matrix composite.

A comprehensive review of the scope and impact of tissue engineering has previously appeared. Tissue-engineered devices have the potential to reduce the annual health-care cost related to tissue loss and end-stage organ failure to the order of $400 billion, eight million invasive surgical procedures, and 65 million hospital days. A common approach to engineer a functional tissue is to place cells derived from a healthy organ or tissue type (identical or similar to the dysfunctional tissue/organ) on or within matrices analogous to host-tissue ECM. These systems can then be enclosed in appropriate membranes that isolate cells from immune rejection following implantation or can be transplanted directly with the administration of drugs that prevent the immune rejection. Another application of these systems is for extracorporeal (outside the patient's body) device support of a dysfunctional organ. In either instance, the success of the engineered tissue depends critically on the interactions of cells with the tissue analogues. The objective of this article is to outline the simplest matrix-design parameters to control these interactions. While organs are comprised of very different tissue types, for the sake of simplicity, this article is primarily pertinent to the tissue engineering of one major organ, the liver. The choice of this tissue type is intended to serve as a comprehensive generalization of many different cell types since in the diversity and complexity of its activities, the liver has few parallels. The development of an artificial liver is also critically awaited, as in the United States alone, 35,000 people, including the many wait listed for the exorbitant liver organ transplants ($300,000), die each year of chronic liver disorders. In many other countries, liver disease is the second leading cause of death.

Type
Tissue Engineering
Copyright
Copyright © Materials Research Society 1996

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1.Langer, R. and Vacanti, J.P., Science 260 (1993) p. 920.CrossRefGoogle Scholar
2.Bissell, D.M., Stamatoglou, S.C., Nermut, M.V., and Hughes, R.C., Eur. J. Cell Biol. 40 (1986) p. 72.Google Scholar
3.Singhvi, R., Kumar, A., Lopez, G.P., Stephanopoulos, G.N., Wang, D.I.C., Whitesides, G.M., and Ingber, D.E., Science 264 (1994) p. 696.CrossRefGoogle Scholar
4.Michalopoulos, G. and Pitot, H.C., Exp. Cell Res. 94 (1975) p. 70.CrossRefGoogle Scholar
5.Dunn, J.C.Y., Yarmush, M.L., Koebe, H.G., and Tompkins, R.G., FASEB J. 3 (1989) p. 174.CrossRefGoogle Scholar
6.Moghe, P.V., Berthiaume, F., Ezzell, R.M., Toner, M., Tompkins, R.G., and Yarmush, M.L., Biomaterials 17 (1996) p. 373.CrossRefGoogle Scholar
7.Toner, M., Tompkins, R.G., and Yarmush, M.L., in Tissue Engineering: Current Perspectives, edited by Bell, E. (Birkhaueser Boston, Cambridge, 1993) p. 92.CrossRefGoogle Scholar
8.Cima, L.G., Ingber, D.E., Vacanti, J.P., and Langer, R., Biotechnol. Bioeng. 38 (1991) p. 145.CrossRefGoogle Scholar
9.Tobe, S., Takei, Y., Kobayashi, K., and Akaike, T., Artif. Organs 16 (1992) p. 526.CrossRefGoogle Scholar
10.Dunn, J.C.Y., Tompkins, R.G., and Yarmush, M.L., Biotechnol. Prog. 7 (1991) p. 237.CrossRefGoogle Scholar
11.Bhatia, S.N., Yarmush, M.L., and Toner, M., J. Biomed. Mater. Res. in press.Google Scholar