Biomedical Engineering Reference
In-Depth Information
functions, such as those involving P 450 enzyme systems, essential for the
effectiveness of extracorporeal liver support devices.
Another area of future research is the use of fetal liver tissue. Fetal tissue
offers significant advantages in that it may be transplanted across the histo-
compatibility barrier, eliminating the need for immunosuppression following
transplantation. However, important ethical questions must be resolved before
fetal tissue can be freely used. Also, recent tissue engineering studies suggest
that by carefully selecting hepatocyte attachment substrates and polymer
supports (scaffoldings) it may be possible to produce bioartificial matrices for
producing liver tissue for transplantation or extracorporeal liver support
systems. 44 Other future approaches for liver support in congenital metabolic
liver disease may involve gene therapy techniques. In theory, a functional gene
could be inserted into defective liver cells to improve a previously deficient liver
function. This approach would allow autologous hepatocyte transplantation
without any need for immunosuppression.
9.8 References
1. Chang, T.M.S. Semipermeable microcapsules. Science 1964; 146: 524±525.
2. Chang TMS, Poznansky MJ. Semipermeable microcapsules containing catalase for
enzyme replacement in acatalasemic mice. Nature 1968; 218: 243±244.
3. Elcin YM, Dixit V, Lewin K, Gitnick G. Xenotransplantation of fetal porcine
hepatocytes in rats using a tissue engineering approach. Artif Organs 1999; 23: 146±
152.
4. Dixit V. Hepatocyte transplantation in liver disease. J Gastro Hepatol (Suppl) 1999;
14: 2±5.
5. Dixit V, Gitnick G. The bioartificial liver ± state-of-the-art. Euro J Surg 1998; 582:
71±76.
6. O'Shea GM, Goosen MFA, Sun AM. Prolonged survival of islets of Langerhans
encapsulated in a biocompatible membrane. Biochem Biophys Acta 1984; 804: 133±
136.
7. Dixit V, Darvasi R, Arthur M, Lewin KJ, Gitnick G. Improved function of
microencapsulated hepatocytes in a hybrid bioartificial liver support system. Artif
Organs 1992; 16: 336±341.
8. Bissell DM, Choun MO. Role of extracellular matrix in normal liver. Scand J
Gastroenterol 1988; 23 (Suppl 151): 1±7.
9. Enat R, Jefferson DM, Ruiz-Opazo N, Gatmaitan Z, Leinwand LA, Reid L.
Hepatocyte proliferation in vitro: its dependence on the use of hormonally defined
medium and substrata of extracellular matrix. Proc Natl Acad Sci USA (Cell Biol)
1984; 81: 1411±1415.
10. Dixit V, Darvasi R, Arthur M, Brezina M, Lewin K, Gitnick G. Restoration of liver
function in Gunn rats without immunosuppression using transplanted
microencapsulated hepatocytes. Hepatology 1990; 12: 1342±1349.
11. Demetriou AA, Levenson SM, Novikoff PM, Novikoff AB, Chowdhury NR,
Whiting JF, Reisner A, Chowdhury JR. Survival, organization, and function of
microcarrier-attached hepatocytes transplanted in rats. Proc Natl Acad Sci USA
1986; 83: 7475±7479.
Search WWH ::




Custom Search