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Integration of single-layer skin hollow fibers and scaffolds develops a three-dimensional hybrid bioreactor for bioartificial livers

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Abstract

Bioartificial liver support systems are expected to be an effective therapy as a “bridge” for liver transplantation or reversible acute liver disease. A major roadblock in the application of bioartificial livers is the need for a bioreactor that fully meets the requirements of hepatocyte culture, mass transfer and immunobarriers. In this study, we developed a three-dimensional hybrid bioreactor (3DHB) on a base of single-layer skin polyethersulfone hollow fibers by integrating with polyurethane scaffolds. The mass transfer of bilirubin and albumin from the intracapillary space to the extracapillary space of the hollow fibers was not significantly different between 3DHBs and hollow fiber bioreactors (HFBs). Cell viability staining showed that high-density hepatocytes were uniformly found in different regions of the 3DHB after 7 days of culture. Liver-specific functions of human mature hepatocytes cultured in the 3DHB, such as albumin secretion, urea production, ammonia removal rate and cytochrome P450 activity, were maintained stably and were significantly higher compared with the HFB. These results indicated that the 3DHB has good mass transfer and improves cell distribution and liver-specific functions. Meanwhile, the ammonia and unconjugated bilirubin concentrations in plasma from patients with liver failure were significantly decreased during 6 h of circulation by hepatocytes cultured in the 3DHB. Most hepatocytes in the 3DHB were viable after 6 h exposure to the patient plasma. We further demonstrated that bioartificial liver systems with 3DHB can remove toxins from and endure the deleterious effects of the patient plasma. Therefore, the 3DHB has the potential to accomplish different actions for the clinical application of bioartificial livers.

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References

  1. Demetriou AA, Brown RS, Busuttil RW Jr, et al. Prospective, randomized, multicenter, controlled trial of a bioartificial liver in treating acute liver failure. Ann Surg. 2004;239(5):660–7 discussion 67–70.

    Article  Google Scholar 

  2. van de Kerkhove MP, Di Florio E, Scuderi V, et al. Phase I clinical trial with the AMC-bioartificial liver. Int J Artif Organs. 2002;25(10):950–9.

    Google Scholar 

  3. van de Kerkhove MP, Di Florio E, Scuderi V, et al. Bridging a patient with acute liver failure to liver transplantation by the AMC-bioartificial liver. Cell Transplant. 2003;12(6):563–8.

    Google Scholar 

  4. van de Kerkhove MP, Hoekstra R, Chamuleau RA, et al. Clinical application of bioartificial liver support systems. Ann Surg. 2004;240(2):216–30.

    Article  Google Scholar 

  5. Soto-Gutierrez A, Kobayashi N, Rivas-Carrillo JD, et al. Reversal of mouse hepatic failure using an implanted liver-assist device containing ES cell-derived hepatocytes. Nat Biotechnol. 2006;24(11):1412–9.

    Article  Google Scholar 

  6. Si-Tayeb K, Noto FK, Nagaoka M, et al. Highly efficient generation of human hepatocyte-like cells from induced pluripotent stem cells. Hepatology. 2010;51(1):297–305.

    Article  Google Scholar 

  7. Wang Y, Zhang Y, Zhang S, et al. Rotating microgravity-bioreactor cultivation enhances the hepatic differentiation of mouse embryonic stem cells on biodegradable polymer scaffolds. Tissue Eng Part A. 2012;18(21–22):2376–85.

    Article  Google Scholar 

  8. Zhang S, Chen L, Liu T, et al. Human umbilical cord matrix stem cells efficiently rescue acute liver failure through paracrine effects rather than hepatic differentiation. Tissue Eng Part A. 2012;18(13–14):1352–64.

    Article  Google Scholar 

  9. Strain AJ, Neuberger JM. A bioartificial liver—state of the art. Science. 2002;295(5557):1005–9.

    Article  Google Scholar 

  10. Poyck PP, Pless G, Hoekstra R, et al. In vitro comparison of two bioartificial liver support systems: MELS Cell Module and AMC-BAL. Int J Artif Organs. 2007;30(3):183–91.

    Google Scholar 

  11. Carpentier B, Gautier A, Legallais C. Artificial and bioartificial liver devices: present and future. Gut. 2009;58(12):1690–702.

    Article  Google Scholar 

  12. Allen JW, Hassanein T, Bhatia SN. Advances in bioartificial liver devices. Hepatology. 2001;34(3):447–55.

    Article  Google Scholar 

  13. Davidson AJ, Ellis MJ, Chaudhuri JB. A theoretical method to improve and optimize the design of bioartificial livers. Biotechnol Bioeng. 2010;106(6):980–8.

    Article  Google Scholar 

  14. Kataoka K, Nagao Y, Nukui T, et al. An organic-inorganic hybrid scaffold for the culture of HepG2 cells in a bioreactor. Biomaterials. 2005;26(15):2509–16.

    Article  Google Scholar 

  15. Torok E, Vogel C, Lutgehetmann M, et al. Morphological and functional analysis of rat hepatocyte spheroids generated on poly(l-lactic acid) polymer in a pulsatile flow bioreactor. Tissue Eng. 2006;12(7):1881–90.

    Article  Google Scholar 

  16. Torok E, Lutgehetmann M, Bierwolf J, et al. Primary human hepatocytes on biodegradable poly(l-lactic acid) matrices: a promising model for improving transplantation efficiency with tissue engineering. Liver Transpl. 2011;17(2):104–14.

    Article  Google Scholar 

  17. Miyoshi H, Ehashi T, Kawai H, et al. Three-dimensional perfusion cultures of mouse and pig fetal liver cells in a packed-bed reactor: effect of medium flow rate on cell numbers and hepatic functions. J Biotechnol. 2010;148(4):226–32.

    Article  Google Scholar 

  18. Zhang S, Liu T, Chen L, et al. Bifunctional polyethersulfone hollow fiber with a porous, single-layer skin for use as a bioartificial liver bioreactor. J Mater Sci Mater Med. 2012;23(8):2001–11.

    Article  Google Scholar 

  19. Zhang SC, Liu T, Wang YJ. Porous and single-skinned polyethersulfone membranes support the growth of HepG2 cells: a potential biomaterial for bioartificial liver systems. J Biomater Appl. 2012;27(3):359–66.

    Article  Google Scholar 

  20. Mitry RR. Isolation of human hepatocytes. Methods Mol Biol. 2009;481:17–23.

    Article  Google Scholar 

  21. Lee KD, Kuo TK, Whang-Peng J, et al. In vitro hepatic differentiation of human mesenchymal stem cells. Hepatology. 2004;40(6):1275–84.

    Article  Google Scholar 

  22. Hoque ME, Mao HQ, Ramakrishna S. Hybrid braided 3-D scaffold for bioartificial liver assist devices. J Biomater Sci Polym Ed. 2007;18(1):45–58.

    Article  Google Scholar 

  23. De Bartolo L, Salerno S, Curcio E, et al. Human hepatocyte functions in a crossed hollow fiber membrane bioreactor. Biomaterials. 2009;30(13):2531–43.

    Article  Google Scholar 

  24. Monga SP, Hout MS, Baun MJ, et al. Mouse fetal liver cells in artificial capillary beds in three-dimensional four-compartment bioreactors. Am J Pathol. 2005;167(5):1279–92.

    Article  Google Scholar 

  25. Gerlach JC, Schnoy N, Encke J, et al. Improved hepatocyte in vitro maintenance in a culture model with woven multicompartment capillary systems: electron microscopy studies. Hepatology. 1995;22(2):546–52.

    Google Scholar 

  26. Zeilinger K, Holland G, Sauer IM, et al. Time course of primary liver cell reorganization in three-dimensional high-density bioreactors for extracorporeal liver support: an immunohistochemical and ultrastructural study. Tissue Eng. 2004;10(7–8):1113–24.

    Google Scholar 

  27. Bettahalli NM, Vicente J, Moroni L, et al. Integration of hollow fiber membranes improves nutrient supply in three-dimensional tissue constructs. Acta Biomater. 2011;7(9):3312–24.

    Article  Google Scholar 

  28. Miskon A, Yamaoka T, Hyon SH, et al. Preservation of porcine hepatocytes in three-dimensional bioreactor at room temperature using epigallocatechin-3-gallate. Tissue Eng Part C Methods. 2009;15(3):345–53.

    Article  Google Scholar 

  29. Funatsu K, Ijima H, Nakazawa K, et al. Hybrid artificial liver using hepatocyte organoid culture. Artif Organs. 2001;25(3):194–200.

    Article  Google Scholar 

  30. Ran F, Nie S, Zhao W, et al. Biocompatibility of modified polyethersulfone membranes by blending an amphiphilic triblock co-polymer of poly(vinyl pyrrolidone)-b-poly(methyl methacrylate)-b-poly(vinyl pyrrolidone). Acta Biomater. 2011;7(9):3370–81.

    Article  Google Scholar 

  31. Eash HJ, Jones HM, Hattler BG, et al. Evaluation of plasma resistant hollow fiber membranes for artificial lungs. ASAIO J. 2004;50(5):491–7.

    Article  Google Scholar 

  32. Lu HF, Lim WS, Zhang PC, et al. Galactosylated poly(vinylidene difluoride) hollow fiber bioreactor for hepatocyte culture. Tissue Eng. 2005;11(11–12):1667–77.

    Article  Google Scholar 

  33. Torok E, Pollok JM, Ma PX, et al. Optimization of hepatocyte spheroid formation for hepatic tissue engineering on three-dimensional biodegradable polymer within a flow bioreactor prior to implantation. Cells Tissues Organs. 2001;169(1):34–41.

    Article  Google Scholar 

  34. Pahernik SA, Thasler WE, Doser M, et al. High density culturing of porcine hepatocytes immobilized on nonwoven polyurethane-based biomatrices. Cells Tissues Organs. 2001;168(3):170–7.

    Article  Google Scholar 

  35. Yamashita Y, Shimada M, Tsujita E, et al. Polyurethane foam/spheroid culture system using human hepatoblastoma cell line (Hep G2) as a possible new hybrid artificial liver. Cell Transplant. 2001;10(8):717–22.

    Google Scholar 

  36. Sakai Y, Naruse K, Nagashima I, et al. A new bioartificial liver using porcine hepatocyte spheroids in high-cell-density suspension perfusion culture: in vitro performance in synthesized culture medium and in 100 % human plasma. Cell Transplant. 1999;8(5):531–41.

    Google Scholar 

  37. Nibourg GA, Hoekstra R, van der Hoeven TV, et al. Effects of acute-liver-failure-plasma exposure on hepatic functionality of HepaRG-AMC-bioartificial liver. Liver Int. 2012;33(4):516–24.

    Article  Google Scholar 

  38. Nieuwoudt M, Kunnike R, Smuts M, et al. Standardization criteria for an ischemic surgical model of acute hepatic failure in pigs. Biomaterials. 2006;27(20):3836–45.

    Article  Google Scholar 

  39. Hung KC, Yong CC, Chen YS, et al. A surgical model of fulminant hepatic failure in rabbits. Liver Int. 2007;27(10):1333–41.

    Google Scholar 

  40. Li LJ, Du WB, Zhang YM, et al. Evaluation of a bioartificial liver based on a nonwoven fabric bioreactor with porcine hepatocytes in pigs. J Hepatol. 2006;44(2):317–24.

    Article  Google Scholar 

  41. Enosawa S, Miyashita T, Saito T, et al. The significant improvement of survival times and pathological parameters by bioartificial liver with recombinant HepG2 in porcine liver failure model. Cell Transplant. 2006;15(10):873–80.

    Article  Google Scholar 

  42. Chen Z, Ding Y, Xu Q, et al. Bioartificial liver inoculated with porcine hepatocyte spheroids for treatment of canine acute liver failure model. Artif Organs. 2003;27(7):613–22.

    Article  Google Scholar 

  43. Cheng YB, Wang YJ, Zhang SC, et al. Response of porcine hepatocytes in primary culture to plasma from severe viral hepatitis patients. World J Gastroenterol. 2005;11(48):7585–90.

    Google Scholar 

  44. Yamada H, Toda G, Yoshiba M, et al. Humoral inhibitor of rat hepatocyte DNA synthesis from patients with fulminant liver failure. Hepatology. 1994;19(5):1133–40.

    Google Scholar 

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Acknowledgments

This research was supported by Grants from the National Natural Science Foundation of China (30800237, 31070880). We gratefully acknowledge Deyuan Science & Technology Development Co., Ltd for preparing the hollow fibers. We thank all members of our laboratory for sharing reagents and advice. We thank American Journal Experts for editorial assistance.

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The authors indicate no potential conflicts of interest.

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Correspondence to Shichang Zhang or Yingjie Wang.

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Zhang, S., Chen, L., Liu, T. et al. Integration of single-layer skin hollow fibers and scaffolds develops a three-dimensional hybrid bioreactor for bioartificial livers. J Mater Sci: Mater Med 25, 207–216 (2014). https://doi.org/10.1007/s10856-013-5033-z

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  • DOI: https://doi.org/10.1007/s10856-013-5033-z

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