Cited by 112Hydrogels: synthesis, properties, applicationsTissue Engineering and Regenerative Medicine3D Printing in Biomedical Research

Hydrogels for Liver Tissue Engineering

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Ye, Shicheng, Boeter, Jochem W.B., Penning, Louis C., Spee, Bart, Schneeberger, Kerstin·2019·Bioengineering

Abstract

Bioengineered livers are promising in vitro models for drug testing, toxicological studies, and as disease models, and might in the future be an alternative for donor organs to treat end-stage liver diseases. Liver tissue engineering (LTE) aims to construct liver models that are physiologically relevant. To make bioengineered livers, the two most important ingredients are hepatic cells and supportive materials such as hydrogels. In the past decades, dozens of hydrogels have been developed to act as supportive materials, and some have been used for in vitro models and formed functional liver constructs. However, currently none of the used hydrogels are suitable for in vivo transplantation. Here, the histology of the human liver and its relationship with LTE is introduced. After that, significant characteristics of hydrogels are described focusing on LTE. Then, both natural and synthetic materials utilized in hydrogels for LTE are reviewed individually. Finally, a conclusion is drawn on a comparison of the different hydrogels and their characteristics and ideal hydrogels are proposed to promote LTE.

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  • Over the past ten years, more than 30 studies have explored dLECM-based hydrogels in liver regeneration.

    “In fact, over the past ten years, more than 30 studies have explored dLECM-based hydrogels in liver regeneration.”

    From From scaffold to function: A systematic review on dLECM-based hydrogels for liver tissue engineering — Fabrication, properties, and translational applications (2026) · cites this paper as [10]

    The Discussion reports that several groups tried decellularized liver ECM as a bioink for liver tissue engineering, supporting the general point that this material has been explored. It does not report more than 30 studies or specify a ten-year period. (LLM, conf=0.85)

    Experimental — accuracy not yet measured
  • dLECM hydrogels can help maintain hepatocyte function in culture, boost angiogenesis, reduce fibrosis, and support the formation of organoid-like structures.

    “Results show these hydrogels can help maintain hepatocyte function in culture, boost angiogenesis, reduce fibrosis, and even support the formation of organoid-like structures.”

    From From scaffold to function: A systematic review on dLECM-based hydrogels for liver tissue engineering — Fabrication, properties, and translational applications (2026) · cites this paper as [10]

    The Discussion reports that decellularized liver ECM has been used as a bioink for liver tissue engineering. Section 3.2 reports maintenance of hepatic functions with other hydrogels, but the passages do not establish these effects for dLECM hydrogels or report that they boost angiogenesis, reduce fibrosis, or form organoid-like structures. (LLM, conf=0.78)

    Experimental — accuracy not yet measured

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References 201 · Cited by 112

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  1. [1]Ananthanarayanan A. Narmada B.C. Mo X. McMillian M. Yu H. Purpose-driven biomaterials research in liver-tissue engineering Trends Biotechnol. 2011 29 110 118 10.1016/j.tibtech.2010.10.006 21129798 · DOI
  2. [2]Du Y. Han R. Ng S. Ni J. Sun W. Wohland T. Ong S.H. Kuleshova L. Yu H. Identification and characterization of a novel prespheroid 3-dimensional hepatocyte monolayer on galactosylated substratum Tissue Eng. 2007 13 1455 1468 10.1089/ten.2006.0381 17518743 · DOI
  3. [3]Ng S. Han R. Chang S. Ni J. Hunziker W. Goryachev A.B. Ong S.H. Yu H. Improved Hepatocyte Excretory Function by Immediate Presentation of Polarity Cues Tissue Eng. 2006 12 2181 2191 10.1089/ten.2006.12.2181 16968159 · DOI
  4. [4]Dash A. Inman W. Hoffmaster K. Sevidal S. Kelly J. Obach R.S. Griffith L.G. Tannenbaum S.R. Liver tissue engineering in the evaluation of drug safety Expert Opin. Drug Metab. Toxicol. 2009 5 1159 1174 10.1517/17425250903160664 19637986 PMC4110978 · DOI
  5. [6]Uygun B.E. Uygun K. Yarmush M.L. 5.541—Liver Tissue Engineering Compr. Biomater. 2011 575 585 10.1016/b978-0-08-055294-1.00193-8 · DOI
  6. [7]Lee J.S. Cho S.-W. Liver tissue engineering: Recent advances in the development of a bio-artificial liver Biotechnol. Bioprocess Eng. 2012 17 427 438 10.1007/s12257-012-0047-9 · DOI
  7. [8]Bhatia S.N. Underhill G.H. Zaret K.S. Fox I.J. Cell and tissue engineering for liver disease Sci. Transl. Med. 2014 6 1 21 10.1126/scitranslmed.3005975 PMC4374645 25031271 · DOI · Paper page
  8. [10]Duan B.-W. Lu S.-C. Wang M.-L. Liu J.-N. Chi P. Lai W. Wu J.-S. Guo Q.-L. Lin D.-D. Liu Y. Liver transplantation in acute-on-chronic liver failure patients with high model for end-stage liver disease (MELD) scores-a single center experience of 100 consecutive cases J. Surg. Res. 2013 18 936 943 10.1016/j.jss.2013.03.008 23558257 · DOI
  9. [11]Kidambi S. Yarmush R.S. Novik E. Chao P. Yarmush M.L. Nahmias Y. Oxygen-mediated enhancement of primary hepatocyte metabolism, functional polarization, gene expression, and drug clearance Proc. Natl. Acad Sci. USA 2009 106 15714 15719 10.1073/pnas.0906820106 19720996 PMC2747185 · DOI · Paper page
  10. [12]Habibullah C.M. Syed I.H. Qamar A. Taher-Uz Z. Human fetal hepatocyte transplantation in patients with fulminant hepatic failure Transplantation 1994 58 951 952 10.1097/00007890-199410270-00016 7940741 · DOI
  11. [14]Mito M. Kusano M. Hepatocyte Transplantation in Man Cell Transpl. 1993 2 65 74 10.1177/096368979300200109 1466053 · DOI
  12. [15]Strom S.C. Fisher R.A. Thompson M.T. Sanyal A.J. Cole P.E. Ham J.M. Posner M.P. Hepatocyte transplantation as a bridge to orthotopic liver transplantation in terminal liver failure Transplantation 1997 63 559 569 10.1097/00007890-199702270-00014 9047152 · DOI
  13. [16]Kisseleva T. Gigante E. Brenner D.A. Recent advances in liver stem cell therapy Curr. Opin. Gastroenterol. 2010 26 395 402 10.1097/MOG.0b013e32833a6bec 20495456 · DOI
  14. [17]Zhang W. Tucker-Kellogg L. Narmada B.C. Venkatraman L. Chang S. Lu Y. Tan N. White J.K. Jia R. Bhowmick S.S. Cell-delivery therapeutics for liver regeneration Adv. Drug Deliv. Rev. 2010 62 814 826 10.1016/j.addr.2010.02.005 20193722 · DOI
  15. [19]Cai J. Zhao Y. Liu Y. Ye F. Song Z. Qin H. Meng S. Chen Y. Zhou R. Song X. Directed differentiation of human embryonic stem cells into functional hepatic cells Hepatology 2007 45 1229 1239 10.1002/hep.21582 17464996 · DOI
  16. [20]Huch M. Dorrell C. Boj S.F. van Es J.H. Li V.S. van de Wetering M. Sato T. Hamer K. Sasaki N. Finegold M.J. In vitro expansion of single Lgr5+ liver stem cells induced by Wnt-driven regeneration Nature 2013 494 247 250 10.1038/nature11826 23354049 PMC3634804 · DOI · Paper page
  17. [21]Si-Tayeb K. Noto F.K. Nagaoka M. Li J. Battle M.A. Duris C. North P.E. Dalton S. Duncan S.A. Highly efficient generation of human hepatocyte-like cells from induced pluripotent stem cells Hepatology 2010 51 297 305 10.1002/hep.23354 19998274 PMC2946078 · DOI · Paper page
  18. [22]Stock P. Bruckner S. Ebensing S. Hempel M. Dollinger M.M. Christ B. The generation of hepatocytes from mesenchymal stem cells and engraftment into murine liver Nat. Protoc. 2010 5 617 627 10.1038/nprot.2010.7 20224562 · DOI
  19. [24]Chen C. Soto-Gutierrez A. Baptista P.M. Spee B. Biotechnology Challenges to In Vitro Maturation of Hepatic Stem Cells Gastroenterology 2018 154 1258 1272 10.1053/j.gastro.2018.01.066 29428334 PMC6237283 · DOI
  20. [25]Levy G. Bomze D. Heinz S. Ramachandran S.D. Noerenberg A. Cohen M. Shibolet O. Sklan E. Braspenning J. Nahmias Y. Long-term culture and expansion of primary human hepatocytes Nat. Biotechnol. 2015 33 1264 1271 10.1038/nbt.3377 26501953 · DOI · Paper page
  21. [28]Sivashanmugam A. Arun Kumar R. Vishnu Priya M. Nair S.V. Jayakumar R. An overview of injectable polymeric hydrogels for tissue engineering Eur. Polym. J. 2015 72 543 565 10.1016/j.eurpolymj.2015.05.014 · DOI · Paper page
  22. [29]Bedian L. Villalba-Rodriguez A.M. Hernandez-Vargas G. Parra-Saldivar R. Iqbal H.M. Bio-based materials with novel characteristics for tissue engineering applications-A review Int. J. Biol. Macromol. 2017 98 837 846 10.1016/j.ijbiomac.2017.02.048 28223133 · DOI
  23. [31]Lee K.Y. Mooney D.J. Hydrogels for Tissue Engineering Chem. Rev. 2001 101 10.1021/cr000108x 11710233 · DOI
  24. [32]Curvello R. Raghuwanshi V.S. Garnier G. Engineering nanocellulose hydrogels for biomedical applications Adv. Colloid Interface Sci. 2019 267 47 61 10.1016/j.cis.2019.03.002 30884359 · DOI
  25. [33]Chiti M.C. Dolmans M.M. Donnez J. Amorim C.A. Fibrin in Reproductive Tissue Engineering: A Review on Its Application as a Biomaterial for Fertility Preservation Ann. Biomed Eng. 2017 45 1650 1663 10.1007/s10439-017-1817-5 28271306 · DOI
  26. [34]Dong C. Lv Y. Application of Collagen Scaffold in Tissue Engineering: Recent Advances and New Perspectives Polymers 2016 8 42 10.3390/polym8020042 30979136 PMC6432532 · DOI
  27. [35]Dash T.K. Konkimalla V.B. Poly-small je, Ukrainian-caprolactone based formulations for drug delivery and tissue engineering: A review J. Control. Release 2012 158 15 33 10.1016/j.jconrel.2011.09.064 21963774 · DOI
  28. [36]Kumar A. Han S.S. PVA-based hydrogels for tissue engineering A review Int. J. Polym. Mater. Polym. Biomater. 2017 66 159 182 10.1080/00914037.2016.1190930 · DOI
  29. [37]Annabi N. Tamayol A. Uquillas J.A. Akbari M. Bertassoni L.E. Cha C. Camci-Unal G. Dokmeci M.R. Peppas N.A. Khademhosseini A. 25th Anniversary Article: Rational Design and Applications of Hydrogels in Regenerative Medicine Adv. Mater. 2014 26 85 124 10.1002/adma.201303233 24741694 PMC3925010 · DOI · Paper page
  30. [38]Drury J.L. Mooney D.J. Hydrogels for tissue engineering: Scaffold design variables and applications Biomaterials 2003 24 4337 4351 10.1016/S0142-9612(03)00340-5 12922147 · DOI · Paper page
  31. [39]Khorshidi S. Karkhaneh A. A review on gradient hydrogel/fiber scaffolds for osteochondral regeneration J. Tissue Eng. Regen. Med. 2018 12 e1974 e1990 10.1002/term.2628 29243352 · DOI
  32. [40]Gradinaru V. Treweek J. Overton K. Deisseroth K. Hydrogel-Tissue Chemistry: Principles and Applications Annu. Rev. Biophys. 2018 47 355 376 10.1146/annurev-biophys-070317-032905 29792820 PMC6359929 · DOI
  33. [41]Jung J. Initiation of Mammalian Liver Development from Endoderm by Fibroblast Growth Factors Science 1999 284 1998 2003 10.1126/science.284.5422.1998 10373120 · DOI · Paper page
  34. [42]Bohm F. Kohler U.A. Speicher T. Werner S. Regulation of liver regeneration by growth factors and cytokines EMBO Mol. Med. 2010 2 294 305 10.1002/emmm.201000085 20652897 PMC3377328 · DOI
  35. [43]Bosch F.X. Ribes J. Díaz M. Cléries R. Primary liver cancer: Worldwide incidence and trends Gastroenterology 2004 127 S5 S16 10.1053/j.gastro.2004.09.011 15508102 · DOI
  36. [44]Rebecca T. Liver regeneration: from myth to mechanism Nat. Rev. Mol. Cell Biol. 2004 5 836 847 15459664
  37. [45]Court F.G. Wemyss-Holden S.A. Dennison A.R. Maddern G.J. The mystery of liver regeneration Br. J. Surg. 2002 89 1089 1095 10.1046/j.1365-2168.2002.02166.x 12190672 · DOI
  38. [46]Yokoyama Y. Nagino M. Nimura Y. Mechanisms of Hepatic Regeneration Following Portal Vein Embolization and Partial Hepatectomy: A Review World J. Surg. 2007 31 367 374 10.1007/s00268-006-0526-2 17219273 · DOI
  39. [47]Fausto N. Riehle K.J. Mechanisms of liver regeneration and their clinical implications J. Hepatobiliary Pancreat. Surg. 2005 12 181 189 10.1007/s00534-005-0979-y 15995805 · DOI
  40. [48]Fausto N. Campbell J.S. Riehle K.J. Liver regeneration Hepatology 2006 43 S45 S53 10.1002/hep.20969 16447274 · DOI · Paper page
  41. [50]Duncan A.W. Dorrell C. Grompe M. Stem cells and liver regeneration Gastroenterology 2009 137 466 481 10.1053/j.gastro.2009.05.044 19470389 PMC3136245 · DOI
  42. [51]Riehle K.J. Dan Y.Y. Campbell J.S. Fausto N. New concepts in liver regeneration J. Gastroenterol. Hepatol. 2011 26 Suppl. 1 203 212 10.1111/j.1440-1746.2010.06539.x 21199532 PMC3077908 · DOI
  43. [52]DeLeve L.D. Liver sinusoidal endothelial cells and liver regeneration J. Clin. Investig. 2013 123 1861 1866 10.1172/JCI66025 23635783 PMC3635729 · DOI
  44. [53]Forbes S.J. Newsome P.N. Liver regeneration-mechanisms and models to clinical application Nat. Rev. Gastroenterol Hepatol 2016 13 473 485 10.1038/nrgastro.2016.97 27353402 · DOI
  45. [54]Timchenko N.A. Aging and liver regeneration Trends Endocrinol. Metab. 2009 20 171 176 10.1016/j.tem.2009.01.005 19359195 · DOI
  46. [55]Zhou Q. Li L. Li J. Stem cells with decellularized liver scaffolds in liver regeneration and their potential clinical applications Liver Int. 2015 35 687 694 10.1111/liv.12581 24797694 · DOI
  47. [57]Willemse J. Lieshout R. van der Laan L.J.W. Verstegen M.M.A. From organoids to organs: Bioengineering liver grafts from hepatic stem cells and matrix Best Pract. Res. Clin. Gastroenterol. 2017 31 151 159 10.1016/j.bpg.2017.03.003 28624103 · DOI
  48. [59]Racanelli V. Rehermann B. The liver as an immunological organ Hepatology 2006 43 S54 S62 10.1002/hep.21060 16447271 · DOI · Paper page
  49. [60]Lin X. Horng M. Sun Y. Shiesh S.C. Chow N.H. Guo X.Z. Computer morphometry for quantitative measurement of liver fibrosis: Comparison with Knodell’s score, colorimetry and conventional description reports J. Gastroenterol. Hepatol. 2010 13 75 80 10.1111/j.1440-1746.1998.tb00549.x 9737576 · DOI
  50. [61]Martinez-Hernandez A. Amenta P.S. The hepatic extracellular matrix Virchows Arch. A 1993 423 77 84 10.1007/BF01606580 8212543 · DOI
  51. [62]Thiery J.P. Duband J.L. Tucker G.C. Cell Migration in the Vertebrate Embryo: Role of Cell Adhesion and Tissue Environment in Pattern Formation Annu. Rev. Cell Biol. 1985 1 91 113 10.1146/annurev.cb.01.110185.000515 3916324 · DOI
  52. [63]Kleinman H.K. Philp D. Hoffman M.P. Role of the extracellular matrix in morphogenesis Curr. Opin. Biotechnol. 2003 14 526 532 10.1016/j.copbio.2003.08.002 14580584 · DOI
  53. [64]Bedossa P. Paradis V. Liver extracellular matrix in health and disease J. Pathol. 2003 200 504 515 10.1002/path.1397 12845618 · DOI
  54. [65]Hynes R.O. The extracellular matrix: Not just pretty fibrils Science 2009 326 1216 1219 10.1126/science.1176009 19965464 PMC3536535 · DOI · Paper page
  55. [66]Baiocchini A. Montaldo C. Conigliaro A. Grimaldi A. Correani V. Mura F. Ciccosanti F. Rotiroti N. Brenna A. Montalbano M. Extracellular Matrix Molecular Remodeling in Human Liver Fibrosis Evolution PLoS ONE 2016 11 e0151736 10.1371/journal.pone.0151736 26998606 PMC4801190 · DOI
  56. [67]Martinez-Hernandez A. The hepatic extracellular matrix. I. Electron immunohistochemical studies in normal rat liver Lab. Investig. 1984 51 57 74 6376944
  57. [68]Rojkind M. Ponce-Noyola P. The Extracellular Matrix of the Liver Collagen Relat. Res. 1982 2 151 175 10.1016/S0174-173X(82)80031-9 7049553 · DOI
  58. [69]Marrone G. Shah V.H. Gracia-Sancho J. Sinusoidal communication in liver fibrosis and regeneration J. Hepatol. 2016 65 608 617 10.1016/j.jhep.2016.04.018 27151183 PMC4992446 · DOI
  59. [70]Zhu C. Coombe D.R. Zheng M.H. Yeoh G.C. Li L. Liver progenitor cell interactions with the extracellular matrix J. Tissue Eng. Regen. Med. 2013 7 757 766 10.1002/term.1470 22467423 · DOI
  60. [71]Klaas M. Kangur T. Viil J. Maemets-Allas K. Minajeva A. Vadi K. Antsov M. Lapidus N. Jarvekulg M. Jaks V. The alterations in the extracellular matrix composition guide the repair of damaged liver tissue Sci. Rep. 2016 6 27398 10.1038/srep27398 27264108 PMC4893701 · DOI
  61. [72]Bemmelen J.M.V. Der Hydrogel und das kristallinische Hydrat des Kupferoxydes Z. Anorg. Chem. 1894 5 466 10.1002/zaac.18940050156 · DOI
  62. [73]Danno A. Gel Formation of Aqueous Solution of Polyvinyl Alcohol Irradiated by Gamma Rays from Cobalt-60 J. Phys. Soc. Jpn. 1958 13 722 727 10.1143/JPSJ.13.722 · DOI
  63. [75]Buwalda S.J. Boere K.W. Dijkstra P.J. Feijen J. Vermonden T. Hennink W.E. Hydrogels in a historical perspective: From simple networks to smart materials J. Control. Release 2014 190 254 273 10.1016/j.jconrel.2014.03.052 24746623 · DOI · Paper page
  64. [76]Vishwakarma S.K. Bardia A. Lakkireddy C. Raju N. Paspala S.A.B. Habeeb M.A. Khan A.A. Intraperitoneal transplantation of bioengineered humanized liver grafts supports failing liver in acute condition Mater. Sci. Eng. C Mater Biol. Appl. 2019 98 861 873 10.1016/j.msec.2019.01.045 30813092 · DOI
  65. [77]Vasanthan K.S. Subramanian A. Krishnan U.M. Sethuraman S. Role of biomaterials, therapeutic molecules and cells for hepatic tissue engineering Biotechnol. Adv. 2012 30 742 752 10.1016/j.biotechadv.2012.01.004 22265845 · DOI
  66. [78]Barbucci R. Hydrogels: Biological Properties and Applications Springer Milan, Italy 2009 1 179
  67. [79]Wang X.H. Li D.P. Wang W.J. Feng Q.L. Cui F.Z. Xu Y.X. Song X.H. van der Werf M. Crosslinked collagen/chitosan matrix for artificial livers Biomaterials 2003 24 3213 3220 10.1016/S0142-9612(03)00170-4 12763448 · DOI
  68. [80]Yu X. Bichtelen A. Wang X. Yan Y. Lin F. Xiong Z. Wu R. Zhang R. Lu Q. Collagen/Chitosan/Heparin Complex with Improved Biocompatibility for Hepatic Tissue Engineering J. Bioact. Compat. Polym. 2016 20 15 28 10.1177/0883911505049653 · DOI
  69. [81]Nair L.S. Laurencin C.T. Biodegradable polymers as biomaterials Prog. Polym. Sci. 2007 32 762 798 10.1016/j.progpolymsci.2007.05.017 · DOI · Paper page
  70. [82]Bhattacharya M. Malinen M.M. Lauren P. Lou Y.R. Kuisma S.W. Kanninen L. Lille M. Corlu A. GuGuen-Guillouzo C. Ikkala O. Nanofibrillar cellulose hydrogel promotes three-dimensional liver cell culture J. Control. Release 2012 164 291 298 10.1016/j.jconrel.2012.06.039 22776290 · DOI
  71. [83]Park U.J. Jeong W. Kwon S.Y. Kim Y. Choi K. Kim H.T. Son D. Fabrication of a Novel Absorbable Vascular Anastomosis Device and Testing in a Pig Liver Transplantation Model Ann. Biomed. Eng. 2019 47 1063 1077 10.1007/s10439-019-02212-5 30680484 · DOI
  72. [84]Li J. Tao R. Wu W. Cao H. Xin J. Li J. Guo J. Jiang L. Gao C. Demetriou A.A. 3D PLGA scaffolds improve differentiation and function of bone marrow mesenchymal stem cell-derived hepatocytes Stem Cells Dev. 2010 19 1427 1436 10.1089/scd.2009.0415 20055663 · DOI
  73. [85]Brandl F. Sommer F. Goepferich A. Rational design of hydrogels for tissue engineering: Impact of physical factors on cell behavior Biomaterials 2007 28 134 146 10.1016/j.biomaterials.2006.09.017 17011028 · DOI
  74. [86]Bomo J. Ezan F. Tiaho F. Bellamri M. Langouet S. Theret N. Baffet G. Increasing 3D Matrix Rigidity Strengthens Proliferation and Spheroid Development of Human Liver Cells in a Constant Growth Factor Environment J. Cell Biochem. 2016 117 708 720 10.1002/jcb.25356 26331987 · DOI
  75. [87]Desai S.S. Tung J.C. Zhou V.X. Grenert J.P. Malato Y. Rezvani M. Espanol-Suner R. Willenbring H. Weaver V.M. Chang T.T. Physiological ranges of matrix rigidity modulate primary mouse hepatocyte function in part through hepatocyte nuclear factor 4 alpha Hepatology 2016 64 261 275 10.1002/hep.28450 26755329 PMC5224931 · DOI · Paper page
  76. [88]Wells R.G. The role of matrix stiffness in regulating cell behavior Hepatology 2008 47 1394 1400 10.1002/hep.22193 18307210 · DOI
  77. [89]Gong H. Agustin J. Wootton D. Zhou J.G. Biomimetic design and fabrication of porous chitosan-gelatin liver scaffolds with hierarchical channel network J. Mater. Sci. Mater. Med. 2014 25 113 120 10.1007/s10856-013-5061-8 24121873 · DOI
  78. [90]Capone S.H. Dufresne M. Rechel M. Fleury M.J. Salsac A.V. Paullier P. Daujat-Chavanieu M. Legallais C. Impact of alginate composition: From bead mechanical properties to encapsulated HepG2/C3A cell activities for in vivo implantation PLoS ONE 2013 8 e62032 10.1371/journal.pone.0062032 23637958 PMC3636232 · DOI
  79. [91]Annabi N. Nichol J.W. Zhong X. Ji C. Koshy S. Khademhosseini A. Dehghani F. Controlling the Porosity and Microarchitecture of Hydrogels for Tissue Engineering Tissue Eng. Part B Rev. 2010 16 371 383 10.1089/ten.teb.2009.0639 20121414 PMC2946907 · DOI
  80. [92]Zhao H. Xu K. Zhu P. Wang C. Chi Q. Smart hydrogels with high tunability of stiffness as a biomimetic cell carrier Cell Biol. Int. 2019 43 84 97 10.1002/cbin.11091 30597680 PMC13397395 · DOI
  81. [93]Park T.G. Perfusion culture of hepatocytes within galactose-derivatized biodegradable poly(lactide-co-glycolide) scaffolds prepared by gas foaming of effervescent salts J. Biomed. Mater. Res. Part B Appl. Biomater. 2010 59 127 135 10.1002/jbm.1224 11745545 · DOI
  82. [94]Park K.H. Bae Y.H. Phenotype of Hepatocyte Spheroids in Arg-Gly-Asp (RGD) Containing a Thermo-Reversible Extracellular Matrix Biosci. Biotechnol. Biochem. 2002 66 1473 1478 10.1271/bbb.66.1473 12224630 · DOI
  83. [95]Ma C.Y.J. Kumar R. Xu X.Y. Mantalaris A. A combined fluid dynamics, mass transport and cell growth model for a three-dimensional perfused biorector for tissue engineering of haematopoietic cells Biochem. Eng. J. 2007 35 1 11 10.1016/j.bej.2006.11.024 · DOI
  84. [96]Wu C. Pan J. Bao Z. Yu Y. Fabrication and characterization of chitosan microcarrier for hepatocyte culture J. Mater. Sci. Mater. Med. 2007 18 2211 2214 10.1007/s10856-007-3071-0 17665121 · DOI
  85. [97]Tripathi A. Melo J.S. Preparation of a sponge-like biocomposite agarose–chitosan scaffold with primary hepatocytes for establishing an in vitro 3D liver tissue model RSC Adv. 2015 5 30701 30710 10.1039/C5RA04153H · DOI
  86. [98]Jaspers M. Dennison M. Mabesoone M.F. MacKintosh F.C. Rowan A.E. Kouwer P.H. Ultra-responsive soft matter from strain-stiffening hydrogels Nat. Commun. 2014 5 5808 10.1038/ncomms6808 25510333 PMC4275588 · DOI
  87. [99]Necas J. Brauner P. Kolar J. Bartosikova L. Hyaluronic acid (hyaluronan)—A review Vet. Med. 2008 53 397 411 10.17221/1930-VETMED · DOI · Paper page
  88. [100]Allison D.D. Grande-Allen K.J. Hyaluronan: A powerful tissue engineering tool Tissue Eng. 2006 12 2131 2140 10.1089/ten.2006.12.2131 16968154 · DOI
  89. [101]Augst A.D. Kong H.J. Mooney D.J. Alginate hydrogels as biomaterials Macromol. Biosci. 2006 6 623 633 10.1002/mabi.200600069 16881042 · DOI
  90. [102]Lee K.Y. Mooney D.J. Alginate: Properties and biomedical applications Prog. Polym. Sci. 2012 37 106 126 10.1016/j.progpolymsci.2011.06.003 22125349 PMC3223967 · DOI
  91. [103]Liu C.Z. Xia Z.D. Han Z.W. Hulley P.A. Triffitt J.T. Czernuszka J.T. Novel 3D collagen scaffolds fabricated by indirect printing technique for tissue engineering J. Biomed. Mater. Res. B Appl. Biomater. 2008 85 519 528 10.1002/jbm.b.30975 18076093 · DOI
  92. [104]Van Vlierberghe S. Dubruel P. Schacht E. Biopolymer-based hydrogels as scaffolds for tissue engineering applications: A review Biomacromolecules 2011 12 1387 1408 10.1021/bm200083n 21388145 · DOI
  93. [105]Klotz B.J. Gawlitta D. Rosenberg A. Malda J. Melchels F.P.W. Gelatin-Methacryloyl Hydrogels: Towards Biofabrication-Based Tissue Repair Trends Biotechnol. 2016 34 394 407 10.1016/j.tibtech.2016.01.002 26867787 PMC5937681 · DOI
  94. [106]Kleinman H.K. Martin G.R. Matrigel: Basement membrane matrix with biological activity Semin. Cancer Biol. 2005 15 378 386 10.1016/j.semcancer.2005.05.004 15975825 · DOI · Paper page
  95. [107]Snyder J.E. Hamid Q. Wang C. Chang R. Emami K. Wu H. Sun W. Bioprinting cell-laden matrigel for radioprotection study of liver by pro-drug conversion in a dual-tissue microfluidic chip Biofabrication 2011 3 034112 10.1088/1758-5082/3/3/034112 21881168 · DOI
  96. [108]Hughes C.S. Postovit L.M. Lajoie G.A. Matrigel: A complex protein mixture required for optimal growth of cell culture Proteomics 2010 10 1886 1890 10.1002/pmic.200900758 20162561 · DOI · Paper page
  97. [109]Currie L.J. Sharpe J.R. Martin R. The use of fibrin glue in skin grafts and tissue-engineered skin replacements: A review Plast. Reconstr. Surg. 2001 108 1713 1726 10.1097/00006534-200111000-00045 11711954 · DOI
  98. [110]Ahmed T.A. Griffith M. Hincke M. Characterization and inhibition of fibrin hydrogel-degrading enzymes during development of tissue engineering scaffolds Tissue Eng. 2007 13 1469 1477 10.1089/ten.2006.0354 17518706 · DOI
  99. [111]Kalia V.C. Ray S. Patel S.K.S. Singh M. Singh G.P. The Dawn of Novel Biotechnological Applications of Polyhydroxyalkanoates Biotechnological Applications of Polyhydroxyalkanoates Kalia V. Springer Singapore 2019
  100. [112]Zhang Y.S. Yue K. Aleman J. Moghaddam K.M. Bakht S.M. Yang J. Jia W. Dell’Erba V. Assawes P. Shin S.R. 3D Bioprinting for Tissue and Organ Fabrication Ann. Biomed. Eng. 2017 45 148 163 10.1007/s10439-016-1612-8 27126775 PMC5085899 · DOI
  101. [113]Mazzocchi A. Devarasetty M. Huntwork R. Soker S. Skardal A. Optimization of collagen type I-hyaluronan hybrid bioink for 3D bioprinted liver microenvironments Biofabrication 2018 11 015003 10.1088/1758-5090/aae543 30270846 PMC8008502 · DOI
  102. [114]Wang X. Yan Y. Xiong Z. Lin F. Wu R. Zhang R. Lu Q. Preparation and evaluation of ammonia-treated collagen/chitosan matrices for liver tissue engineering J. Biomed. Mater. Res. B Appl. Biomater. 2005 75 91 98 10.1002/jbm.b.30264 16015640 · DOI
  103. [115]Wang X. Yan Y. Lin F. Xiong Z. Wu R. Zhang R. Lu Q. Preparation and characterization of a collagen/chitosan/heparin matrix for an implantable bioartificial liver J. Biomater. Sci. Polym. Ed. 2012 16 1063 1080 10.1163/1568562054798554 16231599 · DOI
  104. [116]Wang X. Yan Y. Pan Y. Xiong Z. Liu H. Cheng J. Liu F. Lin F. Wu R. Zhang R. Generation of Three-Dimensional Hepatocyte-Gelatin Structures with Rapid Prototyping System Tissue Eng. 2006 12 83 90 10.1089/ten.2006.12.83 16499445 · DOI
  105. [117]Hussein K.H. Park K.M. Kang K.S. Woo H.M. Heparin-gelatin mixture improves vascular reconstruction efficiency and hepatic function in bioengineered livers Acta Biomater. 2016 38 82 93 10.1016/j.actbio.2016.04.042 27134015 · DOI · Paper page
  106. [118]Wei X. Xiaohong W. Yongnian Y. Renji Z. A Polyurethane-Gelatin Hybrid Construct for Manufacturing Implantable Bioartificial Livers J. Bioact. Compat. Polym. 2008 23 409 422 10.1177/0883911508095517 · DOI
  107. [119]Rozario T. DeSimone D.W. The extracellular matrix in development and morphogenesis: A dynamic view Dev. Biol. 2010 341 126 140 10.1016/j.ydbio.2009.10.026 19854168 PMC2854274 · DOI
  108. [120]Suri S. Han L.H. Zhang W. Singh A. Chen S. Schmidt C.E. Solid freeform fabrication of designer scaffolds of hyaluronic acid for nerve tissue engineering Biomed. Microdevices 2011 13 983 993 10.1007/s10544-011-9568-9 21773726 PMC8638827 · DOI
  109. [121]Turner W.S. Schmelzer E. McClelland R. Wauthier E. Chen W. Reid L.M. Human hepatoblast phenotype maintained by hyaluronan hydrogels J. Biomed. Mater. Res. B Appl. Biomater. 2007 82 156 168 10.1002/jbm.b.30717 17183559 · DOI
  110. [122]Christoffersson J. Aronsson C. Jury M. Selegard R. Aili D. Mandenius C.F. Fabrication of modular hyaluronan-PEG hydrogels to support 3D cultures of hepatocytes in a perfused liver-on-a-chip device Biofabrication 2018 10.1088/1758-5090/aaf657 30523863 · DOI
  111. [123]Bruns H. Kneser U. Holzhüter S. Roth B. Kluth J. Kaufmann P.M. Kluth D. Fiegel H.C. Injectable Liver A Novel Approach Using Fibrin Gel as a Matrix for Culture and Intrahepatic Transplantation of Hepatocytes Tissue Eng. 2005 11 1718 1726 10.1089/ten.2005.11.1718 16411817 · DOI
  112. [124]Wang X. Liu C. Fibrin Hydrogels for Endothelialized Liver Tissue Engineering with a Predesigned Vascular Network Polymers 2018 10 48 10.3390/polym10101048 30960973 PMC6403613 · DOI
  113. [125]Hickey R.D. Naugler W.E. Ectopic expansion of engineered human liver tissue seeds using mature cell populations Hepatology 2018 67 2465 2467 10.1002/hep.29718 29222915 · DOI
  114. [126]Jammalamadaka U. Tappa K. Recent Advances in Biomaterials for 3D Printing and Tissue Engineering J. Funct. Biomater. 2018 9 22 10.3390/jfb9010022 PMC5872108 29494503 · DOI
  115. [127]Kim Y. Kang K. Jeong J. Paik S.S. Kim J.S. Park S.A. Kim W.D. Park J. Choi D. Three-dimensional (3D) printing of mouse primary hepatocytes to generate 3D hepatic structure Ann. Surg. Treat. Res. 2017 92 67 72 10.4174/astr.2017.92.2.67 28203553 PMC5309179 · DOI
  116. [128]Tong X.F. Zhao F.Q. Ren Y.Z. Zhang Y. Cui Y.L. Wang Q.S. Injectable hydrogels based on glycyrrhizin, alginate, and calcium for three-dimensional cell culture in liver tissue engineering J. Biomed. Mater. Res. A 2018 106 3292 3302 10.1002/jbm.a.36528 30242952 · DOI
  117. [129]Lee K.H. Shin S.J. Kim C.B. Kim J.K. Cho Y.W. Chung B.G. Lee S.H. Microfluidic synthesis of pure chitosan microfibers for bio-artificial liver chip Lab. Chip. 2010 10 1328 1334 10.1039/b924987g 20445889 · DOI
  118. [130]Jiankang H. Dichen L. Yaxiong L. Bo Y. Hanxiang Z. Qin L. Bingheng L. Yi L. Preparation of chitosan-gelatin hybrid scaffolds with well-organized microstructures for hepatic tissue engineering Acta Biomater. 2009 5 453 461 10.1016/j.actbio.2008.07.002 18675601 · DOI
  119. [131]Rajendran D. Hussain A. Yip D. Parekh A. Shrirao A. Cho C.H. Long-term liver-specific functions of hepatocytes in electrospun chitosan nanofiber scaffolds coated with fibronectin J. Biomed. Mater. Res. A 2017 105 2119 2128 10.1002/jbm.a.36072 28371246 · DOI
  120. [132]Su Z. Li P. Wu B. Ma H. Wang Y. Liu G. Zeng H. Li Z. Wei X. PHBVHHx scaffolds loaded with umbilical cord-derived mesenchymal stem cells or hepatocyte-like cells differentiated from these cells for liver tissue engineering Mater. Sci. Eng. C Mater. Biol. Appl. 2014 45 374 382 10.1016/j.msec.2014.09.022 25491842 · DOI
  121. [133]Li P. Zhang J. Liu J. Ma H. Liu J. Lie P. Wang Y. Liu G. Zeng H. Li Z. Promoting the recovery of injured liver with poly (3-hydroxybutyrate-co-3-hydroxyvalerate-co-3-hydroxyhexanoate) scaffolds loaded with umbilical cord-derived mesenchymal stem cells Tissue Eng. Part A 2015 21 603 615 10.1089/ten.tea.2013.0331 25273546 PMC4333318 · DOI
  122. [134]Markstedt K. Mantas A. Tournier I. Martinez Avila H. Hagg D. Gatenholm P. 3D Bioprinting Human Chondrocytes with Nanocellulose-Alginate Bioink for Cartilage Tissue Engineering Applications Biomacromolecules 2015 16 1489 1496 10.1021/acs.biomac.5b00188 25806996 · DOI · Paper page
  123. [135]Wu Y. Lin Z.Y. Wenger A.C. Tam K.C. Tang X. 3D bioprinting of liver-mimetic construct with alginate/cellulose nanocrystal hybrid bioink Bioprinting 2018 9 1 6 10.1016/j.bprint.2017.12.001 · DOI
  124. [136]Malinen M.M. Kanninen L.K. Corlu A. Isoniemi H.M. Lou Y.R. Yliperttula M.L. Urtti A.O. Differentiation of liver progenitor cell line to functional organotypic cultures in 3D nanofibrillar cellulose and hyaluronan-gelatin hydrogels Biomaterials 2014 35 5110 5121 10.1016/j.biomaterials.2014.03.020 24698520 · DOI
  125. [137]Jiang S. Liu S. Feng W. PVA hydrogel properties for biomedical application J. Mech. Behav. Biomed. Mater. 2011 4 1228 1233 10.1016/j.jmbbm.2011.04.005 21783131 · DOI
  126. [138]Kouwer P.H. Koepf M. Le Sage V.A. Jaspers M. van Buul A.M. Eksteen-Akeroyd Z.H. Woltinge T. Schwartz E. Kitto H.J. Hoogenboom R. Responsive biomimetic networks from polyisocyanopeptide hydrogels Nature 2013 493 651 655 10.1038/nature11839 23354048 · DOI
  127. [139]Hammink R. Eggermont L.J. Zisis T. Tel J. Figdor C.G. Rowan A.E. Blank K.G. Affinity-Based Purification of Polyisocyanopeptide Bioconjugates Bioconjug. Chem. 2017 28 2560 2568 10.1021/acs.bioconjchem.7b00398 28846388 · DOI
  128. [140]Utech S. Boccaccini A.R. A review of hydrogel-based composites for biomedical applications: enhancement of hydrogel properties by addition of rigid inorganic fillers J. Mater. Sci. 2016 51 271 310 10.1007/s10853-015-9382-5 · DOI
  129. [141]Saito E. Kang H. Taboas J.M. Diggs A. Flanagan C.L. Hollister S.J. Experimental and computational characterization of designed and fabricated 50:50 PLGA porous scaffolds for human trabecular bone applications J. Mater. Sci. Mater. Med. 2010 21 2371 2383 10.1007/s10856-010-4091-8 20524047 · DOI
  130. [142]Sheridan M.H. Shea L.D. Peters M.C. Mooney D.J. Bioabsorbable polymer scaffolds for tissue engineering capable J. Control. Release 2000 64 91 102 10.1016/S0168-3659(99)00138-8 10640648 · DOI
  131. [143]Middleton J.C. Tipton A.J. Synthetic biodegradable polymers as orthopedic devices Biomaterials 2000 21 2335 2346 10.1016/S0142-9612(00)00101-0 11055281 · DOI · Paper page
  132. [144]Lv Q. Hu K. Feng Q. Cui F. Cao C. Preparation and characterization of PLA/fibroin composite and culture of HepG2 (human hepatocellular liver carcinoma cell line) cells Compos. Sci. Technol. 2007 67 3023 3030 10.1016/j.compscitech.2007.05.003 · DOI
  133. [145]Siddiqui N. Asawa S. Birru B. Baadhe R. Rao S. PCL-Based Composite Scaffold Matrices for Tissue Engineering Applications Mol. Biotechnol. 2018 60 506 532 10.1007/s12033-018-0084-5 29761314 · DOI
  134. [146]JANG T.-S. Jung H.-D. Pan H.M. Han W.T. 3D printing of hydrogel composite systems: Recent advances in technology for tissue engineering Int. J. Bioprinting 2018 10.18063/ijb.v4i1.126 PMC7582009 33102909 · DOI
  135. [147]Yoon No D. Lee K.H. Lee J. Lee S.H. 3D liver models on a microplatform: Well-defined culture, engineering of liver tissue and liver-on-a-chip Lab. Chip. 2015 15 3822 3837 10.1039/C5LC00611B 26279012 · DOI · Paper page
  136. [148]Perez R.A. Jung C.R. Kim H.W. Biomaterials and Culture Technologies for Regenerative Therapy of Liver Tissue Adv. Healthc. Mater. 2017 6 10.1002/adhm.201600791 27860372 · DOI
  137. [149]Schepers A. Li C. Chhabra A. Seney B.T. Bhatia S. Engineering a perfusable 3D human liver platform from iPS cells Lab. Chip. 2016 16 2644 2653 10.1039/C6LC00598E 27296616 PMC5318999 · DOI
  138. [151]Celikkin N. Simó Padial J. Costantini M. Hendrikse H. Cohn R. Wilson C. Rowan A. Święszkowski W. 3D Printing of Thermoresponsive Polyisocyanide (PIC) Hydrogels as Bioink and Fugitive Material for Tissue Engineering Polymers 2018 10 555 10.3390/polym10050555 PMC6415434 30966589 · DOI
  139. [152]Liu Y. Geever L.M. Kennedy J.E. Higginbotham C.L. Cahill P.A. McGuinness G.B. Thermal behavior and mechanical properties of physically crosslinked PVA/Gelatin hydrogels J. Mech. Behav. Biomed. Mater. 2010 3 203 209 10.1016/j.jmbbm.2009.07.001 20129419 · DOI
  140. [153]Moscato S. Ronca F. Campani D. Danti S. Poly(vinyl alcohol)/gelatin Hydrogels Cultured with HepG2 Cells as a 3D Model of Hepatocellular Carcinoma: A Morphological Study J. Funct. Biomater. 2015 6 16 32 10.3390/jfb6010016 25590431 PMC4384098 · DOI
  141. [154]Kim S.S. Utsunomiya H. Koski J.A. Wu B.M. Cima M.J. Sohn J. Mukai K. Griffith L.G. Vacanti J.P. Survival and function of hepatocytes on a novel three-dimensional synthetic biodegradable polymer scaffold with an intrinsic network of channels Ann. Surg. 1998 228 8 13 10.1097/00000658-199807000-00002 9671060 PMC1191421 · DOI
  142. [155]Kasuya J. Sudo R. Tamogami R. Masuda G. Mitaka T. Ikeda M. Tanishita K. Reconstruction of 3D stacked hepatocyte tissues using degradable, microporous poly(d,l-lactide-co-glycolide) membranes Biomaterials 2012 33 2693 2700 10.1016/j.biomaterials.2011.12.039 22236830 · DOI
  143. [156]Kobayashi S. Nagano H. Marubashi S. Wada H. Eguchi H. Takeda Y. Tanemura M. Doki Y. Mori M. Fibrin sealant with PGA felt for prevention of bile leakage after liver resection Hepatogastroenterology 2012 59 2564 2568 10.5754/hge10315 23178623 · DOI
  144. [157]Riccalton-Banks L. Liew C. Bhandari R. Fry J. Shakesheff K. Long-Term Culture of Functional Liver Tissue Three-Dimensional Coculture of Primary Hepatocytes and Stellate Cells Tissue Eng. 2003 9 401 410 10.1089/107632703322066589 12857408 · DOI
  145. [158]Davis M.W. Vacanti J.P. Toward development of an implantable tissue engineered liver Biomaterials 1996 17 365 372 10.1016/0142-9612(96)85575-X 8745334 · DOI
  146. [159]Feng Z.Q. Chu X.H. Huang N.P. Leach M.K. Wang G. Wang Y.C. Ding Y.T. Gu Z.Z. Rat hepatocyte aggregate formation on discrete aligned nanofibers of type-I collagen-coated poly(L-lactic acid) Biomaterials 2010 31 3604 3612 10.1016/j.biomaterials.2010.01.080 20149442 · DOI
  147. [160]Lee J.W. Choi Y.J. Yong W.J. Pati F. Shim J.H. Kang K.S. Kang I.H. Park J. Cho D.W. Development of a 3D cell printed construct considering angiogenesis for liver tissue engineering Biofabrication 2016 8 015007 10.1088/1758-5090/8/1/015007 26756962 · DOI
  148. [161]Grant R. Hay D.C. Callanan A. A Drug-Induced Hybrid Electrospun Poly-Capro-Lactone: Cell-Derived Extracellular Matrix Scaffold for Liver Tissue Engineering Tissue Eng. Part A 2017 23 650 662 10.1089/ten.tea.2016.0419 28437180 · DOI
  149. [162]Hashemi S.M. Soleimani M. Zargarian S.S. Haddadi-Asl V. Ahmadbeigi N. Soudi S. Gheisari Y. Hajarizadeh A. Mohammadi Y. In vitro differentiation of human cord blood-derived unrestricted somatic stem cells into hepatocyte-like cells on poly(epsilon-caprolactone) nanofiber scaffolds Cells Tissues Organs 2009 190 135 149 10.1159/000187716 19092233 · DOI
  150. [163]Semnani D. Naghashzargar E. Hadjianfar M. Dehghan Manshadi F. Mohammadi S. Karbasi S. Effaty F. Evaluation of PCL/chitosan electrospun nanofibers for liver tissue engineering Int. J. Polym. Mater. Polym. Biomater. 2016 66 149 157 10.1080/00914037.2016.1190931 · DOI
  151. [164]Tan W.J. Teo G.P. Liao K. Leong K.W. Mao H.Q. Chan V. Adhesion contact dynamics of primary hepatocytes on poly(ethylene terephthalate) surface Biomaterials 2005 26 891 898 10.1016/j.biomaterials.2004.03.041 15353200 · DOI
  152. [165]Janorkar A.V. Rajagopalan P. Yarmush M.L. Megeed Z. The use of elastin-like polypeptide-polyelectrolyte complexes to control hepatocyte morphology and function in vitro Biomaterials 2008 29 625 632 10.1016/j.biomaterials.2007.10.022 18006054 · DOI
  153. [166]Cho C.S. Seo S.J. Park I.K. Kim S.H. Kim T.H. Hoshiba T. Harada I. Akaike T. Galactose-carrying polymers as extracellular matrices for liver tissue engineering Biomaterials 2006 27 576 585 10.1016/j.biomaterials.2005.06.008 16084586 · DOI
  154. [167]Zhang Y. Wang Q.S. Yan K. Qi Y. Wang G.F. Cui Y.L. Preparation, characterization, and evaluation of genipin crosslinked chitosan/gelatin three-dimensional scaffolds for liver tissue engineering applications J. Biomed. Mater. Res. A 2016 104 1863 1870 10.1002/jbm.a.35717 27027247 · DOI
  155. [168]Yan Y. Wang X. Pan Y. Liu H. Cheng J. Xiong Z. Lin F. Wu R. Zhang R. Lu Q. Fabrication of viable tissue-engineered constructs with 3D cell-assembly technique Biomaterials 2005 26 5864 5871 10.1016/j.biomaterials.2005.02.027 15949552 · DOI
  156. [169]Jiankang H. Dichen L. Yaxiong L. Bo Y. Bingheng L. Qin L. Fabrication and characterization of chitosan/gelatin porous scaffolds with predefined internal microstructures Polymer 2007 48 4578 4588 10.1016/j.polymer.2007.05.048 · DOI
  157. [170]Yang Z. Xu L.S. Yin F. Shi Y.Q. Han Y. Zhang L. Jin H.F. Nie Y.Z. Wang J.B. Hao X. In vitro and in vivo characterization of silk fibroin/gelatin composite scaffolds for liver tissue engineering J. Dig. Dis. 2012 13 168 178 10.1111/j.1751-2980.2011.00566.x 22356312 · DOI
  158. [171]Fan J. Shang Y. Yuan Y. Yang J. Preparation and characterization of chitosan/galactosylated hyaluronic acid scaffolds for primary hepatocytes culture J. Mater. Sci. Mater. Med. 2010 21 319 327 10.1007/s10856-009-3833-y 19641850 · DOI
  159. [172]Turner R.A. Wauthier E. Lozoya O. McClelland R. Bowsher J.E. Barbier C. Prestwich G. Hsu E. Gerber D.A. Reid L.M. Successful transplantation of human hepatic stem cells with restricted localization to liver using hyaluronan grafts Hepatology 2013 57 775 784 10.1002/hep.26065 22996260 PMC3583296 · DOI
  160. [173]Dvir-Ginzberg M. Gamlieli-Bonshtein I. Agbaria R. Cohen S. Liver Tissue Engineering within Alginate Scaffolds Effects of Cell-Seeding Density on Hepatocyte Viability, Morphology, and Function Tissue Eng. 2003 9 757 766 10.1089/107632703768247430 13678452 · DOI
  161. [174]Kilbride P. Mahbubani K.T. Saeb-Parsy K. Morris G.J. Engaging Cold to Upregulate Cell Proliferation in Alginate-Encapsulated Liver Spheroids Tissue Eng. Part C Methods 2017 23 455 464 10.1089/ten.tec.2017.0131 28727981 · DOI
  162. [175]Glicklis R. Shapiro L. Agbaria R. Merchuk J.C. Cohen S. Hepatocyte behavior within three-dimensional porous alginate scaffolds Biotechnol. Bioeng. 2000 67 344 353 10.1002/(SICI)1097-0290(20000205)67:3<344::AID-BIT11>3.0.CO;2-2 10620265 · DOI
  163. [176]Yang J. Chung T.W. Nagaoka M. Goto M. Cho C.-S. Akaike T. Hepatocyte-specific porous polymer-scaffolds of alginate-galactosylated chitosan sponge for liver-tissue engineering Biotechnol. Lett. 2001 23 1385 1389 10.1023/A:1011600414225 · DOI
  164. [177]Wang B. Hu Q. Wan T. Yang F. Cui L. Hu S. Gong B. Li M. Zheng Q.C. Porous Lactose-Modified Chitosan Scaffold for Liver Tissue Engineering: Influence of Galactose Moieties on Cell Attachment and Mechanical Stability Int. J. Polym. Sci. 2016 2016 1 8 10.1155/2016/2862738 · DOI
  165. [178]She Z. Jin C. Huang Z. Zhang B. Feng Q. Xu Y. Silk fibroin/chitosan scaffold: Preparation, characterization, and culture with HepG2 cell J. Mater. Sci. Mater. Med. 2008 19 3545 3553 10.1007/s10856-008-3526-y 18622765 · DOI
  166. [179]She Z. Zhang B. Jin C. Feng Q. Xu Y. Preparation and in vitro degradation of porous three-dimensional silk fibroin/chitosan scaffold Polym. Degrad. Stab. 2008 93 1316 1322 10.1016/j.polymdegradstab.2008.04.001 · DOI
  167. [180]Lewis P.L. Shah R.N. 3D Printing for Liver Tissue Engineering: Current Approaches and Future Challenges Curr. Transplant. Rep. 2016 3 100 108 10.1007/s40472-016-0084-y · DOI
  168. [181]Miller J.S. Stevens K.R. Yang M.T. Baker B.M. Nguyen D.H. Cohen D.M. Toro E. Chen A.A. Galie P.A. Yu X. Rapid casting of patterned vascular networks for perfusable engineered three-dimensional tissues Nat. Mater. 2012 11 768 774 10.1038/nmat3357 22751181 PMC3586565 · DOI · Paper page
  169. [182]Gou M. Qu X. Zhu W. Xiang M. Yang J. Zhang K. Wei Y. Chen S. Bio-inspired detoxification using 3D-printed hydrogel nanocomposites Nat. Commun. 2014 5 3774 10.1038/ncomms4774 24805923 PMC4024742 · DOI
  170. [183]Underhill G.H. Chen A.A. Albrecht D.R. Bhatia S.N. Assessment of hepatocellular function within PEG hydrogels Biomaterials 2007 28 256 270 10.1016/j.biomaterials.2006.08.043 16979755 · DOI
  171. [184]Hammond J.S. Gilbert T.W. Howard D. Zaitoun A. Michalopoulos G. Shakesheff K.M. Beckingham I.J. Badylak S.F. Scaffolds containing growth factors and extracellular matrix induce hepatocyte proliferation and cell migration in normal and regenerating rat liver J. Hepatol. 2011 54 279 287 10.1016/j.jhep.2010.06.040 21126791 · DOI
  172. [185]Stevens K.R. Miller J.S. Blakely B.L. Chen C.S. Bhatia S.N. Degradable hydrogels derived from PEG-diacrylamide for hepatic tissue engineering J. Biomed. Mater. Res. A 2015 103 3331 3338 10.1002/jbm.a.35478 25851120 PMC4890565 · DOI
  173. [186]Zimoch J. Padial J.S. Klar A.S. Vallmajo-Martin Q. Meuli M. Biedermann T. Wilson C.J. Rowan A. Reichmann E. Polyisocyanopeptide hydrogels: A novel thermo-responsive hydrogel supporting pre-vascularization and the development of organotypic structures Acta Biomater. 2018 70 129 139 10.1016/j.actbio.2018.01.042 29454158 · DOI
  174. [187]Hasirci V. Berthiaume F. Bondre S.P. Gresser J.D. Trantolo D.J. Toner M. Wise D.L. Expression of Liver-Specific Functions by Rat Hepatocytes Seeded in Treated Poly(Lactic-co-Glycolic) Acid Biodegradable Foams Tissue Eng. 2001 7 385 394 10.1089/10763270152436445 11506728 · DOI
  175. [188]Wang X. Rijff B.L. Khang G. A building-block approach to 3D printing a multichannel, organ-regenerative scaffold J. Tissue Eng. Regen. Med. 2017 11 1403 1411 10.1002/term.2038 26123711 · DOI
  176. [189]Bishi D.K. Mathapati S. Venugopal J.R. Guhathakurta S. Cherian K.M. Verma R.S. Ramakrishna S. A Patient-Inspired Ex Vivo Liver Tissue Engineering Approach with Autologous Mesenchymal Stem Cells and Hepatogenic Serum Adv. Healthc. Mater. 2016 5 1058 1070 10.1002/adhm.201500897 26890619 · DOI
  177. [190]Huang H. Oizumi S. Kojima N. Niino T. Sakai Y. Avidin-biotin binding-based cell seeding and perfusion culture of liver-derived cells in a porous scaffold with a three-dimensional interconnected flow-channel network Biomaterials 2007 28 3815 3823 10.1016/j.biomaterials.2007.05.004 17544499 · DOI
  178. [191]Rad A.T. Ali N. Kotturi H.S. Yazdimamaghani M. Smay J. Vashaee D. Tayebi L. Conducting scaffolds for liver tissue engineering J. Biomed. Mater. Res. A 2014 102 4169 4181 10.1002/jbm.a.35080 24443356 · DOI
  179. [192]Blouin A. Bolender R.P. Weibel E.R. Distribution of organelles and membranes between hepatocytes and nonhepatocytes in the rat liver parenchyma. A stereological study J. Cell Biol. 1977 72 441 455 10.1083/jcb.72.2.441 833203 PMC2110997 · DOI
  180. [193]Page D.T. Garvey J.S. Isolation and characterization of hepatocytes and Kupffer cells J. Immunol. Methods 1979 27 159 173 10.1016/0022-1759(79)90262-X 458170 · DOI
  181. [194]Lee H. Han W. Kim H. Ha D.H. Jang J. Kim B.S. Cho D.W. Development of Liver Decellularized Extracellular Matrix Bioink for Three-Dimensional Cell Printing-Based Liver Tissue Engineering Biomacromolecules 2017 18 1229 1237 10.1021/acs.biomac.6b01908 28277649 · DOI
  182. [195]Mazza G. Al-Akkad W. Rombouts K. Pinzani M. Liver tissue engineering: From implantable tissue to whole organ engineering Hepatol. Commun. 2018 2 131 141 10.1002/hep4.1136 29404520 PMC5796330 · DOI
  183. [196]Ambekar R.S. Kandasubramanian B. Progress in the Advancement of Porous Biopolymer Scaffold: Tissue Engineering Application Ind. Eng. Chem. Res. 2019 58 6163 6194 10.1021/acs.iecr.8b05334 · DOI
  184. [197]Lewis P.L. Green R.M. Shah R.N. 3D-printed gelatin scaffolds of differing pore geometry modulate hepatocyte function and gene expression Acta Biomater. 2018 69 63 70 10.1016/j.actbio.2017.12.042 29317370 PMC5831494 · DOI

Authors
Ye, S., Boeter, J. W. B., Penning, L. C., Spee, B., & Schneeberger, K.
Affiliations
Utrecht University (NL)
Corresponding author
Schneeberger, Kerstin
Venue
Bioengineering
Publisher
MDPI AG
Published
2019-07-05
Volume
6
Issue
3
Pages
59
ISSN
2306-5354 (ISSN-L)
OpenAlex
W2954064367
Cited by
112
References
201
Citations by year
2026: 8 · 2025: 16 · 2024: 22 · 2023: 21 · 2022: 17 · 2021: 15 · 2020: 11 · 2019: 2
FWCI
0.75
Type
journal article
Language
en
Open access
Locations
  • Bioengineering (publishedVersion, cc-by)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
  • Utrecht University Repository (Utrecht University) (submittedVersion, other-oa)
  • Informationszentrum Lebenswissenschaften (ZB MED) (submittedVersion, cc-by)
Funders
  • Nederlandse Organisatie voor Wetenschappelijk Onderzoek (016.Veni.198.021)
  • China Scholarship Council (CSC201808310180)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Medicine › Hydrogels: synthesis, properties, applications
  • Health Sciences › Medicine › Surgery › Tissue Engineering and Regenerative Medicine
  • Physical Sciences › Engineering › Biomedical Engineering › 3D Printing in Biomedical Research
Keywords
hydrogels, liver tissue engineering, in vitro liver models, in vivo transplantation, natural hydrogels, synthetic hydrogels, liver histopathology, hepatocytes, drug testing, toxicology, end-stage liver disease

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

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