Literature DB >> 30143060

Biofabrication of Autologous Human Hepatocytes for Transplantation: How Do We Get There?

Nandini Agarwal1, Branimir Popovic2, Nicole J Martucci2, Nicolas A Fraunhoffer2, Alejandro Soto-Gutierrez2.   

Abstract

Directed differentiation of hepatocytes from induced pluripotent stem cells (iPSCs) holds promise as source material for treating some liver disorders. The unlimited availability of perfectly differentiated iPSC-derived hepatocytes will dramatically facilitate cell therapies. While systems to manufacture large quantities of iPSC-derived cells have been developed, we have been unable to generate and maintain stable and mature adult liver cells ex vivo. This short review highlights important challenges and possible solutions to the current state of hepatocyte biofabrication for cellular therapies to treat liver diseases. Successful cell transplantation will require optimizing the best cell function, overcoming limitations to cell numbers and safety, as well as a number of other challenges. Collaboration among scientists, clinicians, and industry is critical for generating new autologous stem cell-based therapies to treat liver diseases.

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Year:  2018        PMID: 30143060      PMCID: PMC6466180          DOI: 10.3727/105221618X15350366478989

Source DB:  PubMed          Journal:  Gene Expr        ISSN: 1052-2166


  55 in total

1.  Wnt/β-catenin signalling regulates Sox17 expression and is essential for organizer and endoderm formation in the mouse.

Authors:  Silvia Engert; Ingo Burtscher; W Perry Liao; Stanimir Dulev; Gunnar Schotta; Heiko Lickert
Journal:  Development       Date:  2013-07-03       Impact factor: 6.868

Review 2.  Cell therapy as a strategy to minimize maintenance immunosuppression in solid organ transplant recipients.

Authors:  Edward K Geissler; James A Hutchinson
Journal:  Curr Opin Organ Transplant       Date:  2013-08       Impact factor: 2.640

3.  A Novel Amino Lipid Series for mRNA Delivery: Improved Endosomal Escape and Sustained Pharmacology and Safety in Non-human Primates.

Authors:  Staci Sabnis; E Sathyajith Kumarasinghe; Timothy Salerno; Cosmin Mihai; Tatiana Ketova; Joseph J Senn; Andy Lynn; Alex Bulychev; Iain McFadyen; Joyce Chan; Örn Almarsson; Matthew G Stanton; Kerry E Benenato
Journal:  Mol Ther       Date:  2018-03-14       Impact factor: 11.454

4.  Efficient delivery of genome-editing proteins using bioreducible lipid nanoparticles.

Authors:  Ming Wang; John A Zuris; Fantao Meng; Holly Rees; Shuo Sun; Pu Deng; Yong Han; Xue Gao; Dimitra Pouli; Qi Wu; Irene Georgakoudi; David R Liu; Qiaobing Xu
Journal:  Proc Natl Acad Sci U S A       Date:  2016-02-29       Impact factor: 11.205

5.  CRISPR/Cas9-mediated genome engineering: an adeno-associated viral (AAV) vector toolbox.

Authors:  Elena Senís; Chronis Fatouros; Stefanie Große; Ellen Wiedtke; Dominik Niopek; Ann-Kristin Mueller; Kathleen Börner; Dirk Grimm
Journal:  Biotechnol J       Date:  2014-10-06       Impact factor: 4.677

6.  Activin and BMP4 synergistically promote formation of definitive endoderm in human embryonic stem cells.

Authors:  Adrian K K Teo; Yusuf Ali; Kee Yew Wong; Hiram Chipperfield; Akila Sadasivam; Yogavalli Poobalan; Ee Kim Tan; Siew Tein Wang; Suman Abraham; Norihiro Tsuneyoshi; Lawrence W Stanton; N Ray Dunn
Journal:  Stem Cells       Date:  2012-04       Impact factor: 6.277

7.  Induction of pluripotent stem cells from adult human fibroblasts by defined factors.

Authors:  Kazutoshi Takahashi; Koji Tanabe; Mari Ohnuki; Megumi Narita; Tomoko Ichisaka; Kiichiro Tomoda; Shinya Yamanaka
Journal:  Cell       Date:  2007-11-30       Impact factor: 41.582

8.  Mouse liver repopulation with hepatocytes generated from human fibroblasts.

Authors:  Saiyong Zhu; Milad Rezvani; Jack Harbell; Aras N Mattis; Alan R Wolfe; Leslie Z Benet; Holger Willenbring; Sheng Ding
Journal:  Nature       Date:  2014-02-23       Impact factor: 49.962

9.  A dual AAV system enables the Cas9-mediated correction of a metabolic liver disease in newborn mice.

Authors:  Yang Yang; Lili Wang; Peter Bell; Deirdre McMenamin; Zhenning He; John White; Hongwei Yu; Chenyu Xu; Hiroki Morizono; Kiran Musunuru; Mark L Batshaw; James M Wilson
Journal:  Nat Biotechnol       Date:  2016-02-01       Impact factor: 54.908

10.  CRISPR Correction of a Homozygous Low-Density Lipoprotein Receptor Mutation in Familial Hypercholesterolemia Induced Pluripotent Stem Cells.

Authors:  Linda Omer; Elizabeth A Hudson; Shirong Zheng; James B Hoying; Yuan Shan; Nolan L Boyd
Journal:  Hepatol Commun       Date:  2017-10-16
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  1 in total

Review 1.  Induced pluripotent stem cells for the treatment of liver diseases: challenges and perspectives from a clinical viewpoint.

Authors:  Eugenia Pareja; M José Gómez-Lechón; Laia Tolosa
Journal:  Ann Transl Med       Date:  2020-04
  1 in total

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