Literature DB >> 25366164

Bioartificial livers in vitro and in vivo: tailoring biocomponents to the expanding variety of applications.

Martien van Wenum1, Robert Afm Chamuleau, Thomas M van Gulik, Adriaan Siliakus, Jurgen Seppen, Ruurdtje Hoekstra.   

Abstract

INTRODUCTION: Bioartificial livers (BALs) were originally developed to treat patients suffering from severe liver failure and relied on primary hepatocytes or on hepatoblastoma-derived cell lines. Currently, new in vitro BAL applications are emerging, including drug toxicity testing, disease modeling and basic clinical research, and in recent years, advances in the field of stem cell biology have resulted in potential alternative cell sources. AREAS COVERED: This review identifies the demands of clinical and in vitro BAL applications to their biocomponent and summarizes the functionality and developmental state of BAL technology and cell types currently available. Relevant studies identified by searching the MEDLINE database until April 2014 were reviewed, supplemented with some of our own unpublished data. EXPERT OPINION: BALs have the potential to meet demands currently left unmet in both clinical and in vitro applications. All the reviewed biocomponents show limitations towards one or more BAL applications. However, the generation of stem cell-derived hepatocyte-like cells is progressing rapidly, so the criteria for patient-specific drug toxicity screening and disease modeling are probably met in the near future. HepaRG cells are the most promising biocomponent for clinical BAL application, based on their proliferative and differentiation capacity.

Entities:  

Keywords:  HepaRG; bioartificial liver; drug induced liver injury; hepatitis; hepatocyte; hepatocyte like cell; iHEP; induced pluripotent stem cell; liver; stem cell

Mesh:

Year:  2014        PMID: 25366164     DOI: 10.1517/14712598.2014.950651

Source DB:  PubMed          Journal:  Expert Opin Biol Ther        ISSN: 1471-2598            Impact factor:   4.388


  9 in total

Review 1.  Cell therapy in chronic liver disease.

Authors:  Clara T Nicolas; Yujia Wang; Scott L Nyberg
Journal:  Curr Opin Gastroenterol       Date:  2016-05       Impact factor: 3.287

2.  Zebularine upregulates expression of CYP genes through inhibition of DNMT1 and PKR in HepG2 cells.

Authors:  Kazuaki Nakamura; Kazuko Aizawa; Kyaw Htet Aung; Junji Yamauchi; Akito Tanoue
Journal:  Sci Rep       Date:  2017-01-23       Impact factor: 4.379

3.  Selecting Cells for Bioartificial Liver Devices and the Importance of a 3D Culture Environment: A Functional Comparison between the HepaRG and C3A Cell Lines.

Authors:  Martien van Wenum; Aziza A A Adam; Theodorus B M Hakvoort; Erik J Hendriks; Valery Shevchenko; Thomas M van Gulik; Robert A F M Chamuleau; Ruurdtje Hoekstra
Journal:  Int J Biol Sci       Date:  2016-06-24       Impact factor: 6.580

4.  A practice-changing culture method relying on shaking substantially increases mitochondrial energy metabolism and functionality of human liver cell lines.

Authors:  Aziza A A Adam; Vincent A van der Mark; Joanne M Donkers; Manon E Wildenberg; Ronald P J Oude Elferink; Robert A F M Chamuleau; Ruurdtje Hoekstra
Journal:  PLoS One       Date:  2018-04-19       Impact factor: 3.240

5.  Genome-wide expression profiling reveals increased stability and mitochondrial energy metabolism of the human liver cell line HepaRG-CAR.

Authors:  Aziza A A Adam; Aldo Jongejan; Perry D Moerland; Vincent A van der Mark; Ronald P Oude Elferink; Robert A F M Chamuleau; Ruurdtje Hoekstra
Journal:  Cytotechnology       Date:  2020-03-04       Impact factor: 2.058

Review 6.  End-stage liver failure: filling the treatment gap at the intensive care unit.

Authors:  Robert A F M Chamuleau; Ruurdtje Hoekstra
Journal:  J Artif Organs       Date:  2019-09-18       Impact factor: 1.731

Review 7.  Two Effective Routes for Removing Lineage Restriction Roadblocks: From Somatic Cells to Hepatocytes.

Authors:  Chenxia Hu; Lanjuan Li
Journal:  Int J Mol Sci       Date:  2015-09-01       Impact factor: 5.923

8.  Reversibly immortalized hepatic progenitor cell line containing double suicide genes.

Authors:  Shu-Yu Fang; Chao-Qun Hu; Meng-Nan Liu; Li Tao; Yi Wang; Meng-Jia Gong; Yun He; Tong-Chuan He; Yang Bi
Journal:  Int J Mol Med       Date:  2018-08-02       Impact factor: 4.101

9.  Oxygen drives hepatocyte differentiation and phenotype stability in liver cell lines.

Authors:  Martien van Wenum; Aziza A A Adam; Vincent A van der Mark; Jung-Chin Chang; Manon E Wildenberg; Erik J Hendriks; Aldo Jongejan; Perry D Moerland; Thomas M van Gulik; Ronald P Oude Elferink; Robert A F M Chamuleau; Ruurdtje Hoekstra
Journal:  J Cell Commun Signal       Date:  2018-02-04       Impact factor: 5.782

  9 in total

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