Literature DB >> 26074681

Cell therapy from bench to bedside: Hepatocytes from fibroblasts - the truth and myth of transdifferentiation.

Madhusudana Girija Sanal1.   

Abstract

Hepatocyte transplantation is an alternative to liver transplantation in certain disorders such as inherited liver diseases and liver failure. It is a relatively less complicated surgical procedure, and has the advantage that it can be repeated several times if unsuccessful. Another advantage is that hepatocytes can be isolated from partly damaged livers which are not suitable for liver transplantation. Despite these advantages hepatocyte transplantation is less popular. Important issues are poor engraftment of the transplanted cells and the scarcity of donor hepatocytes. Generation of "hepatocyte like cells"/iHeps from embryonic stem cells (ES) and induced pluripotent stem cells (iPSCs) by directed differentiation is an emerging solution to the latter issue. Direct conversation or trans-differentiation of fibroblasts to "hepatocyte like cells" is another way which is, being explored. However this method has several inherent and technical disadvantages compared to the directed differentiation from ES or iPSC. There are several methods claiming to be "highly efficient" for generating "highly functional" "hepatocyte like cells". Currently different groups are working independently and coming up with differentiation protocols and each group claiming an advantage for their protocol. Directed differentiation protocols need to be designed, compared, analyzed and tweaked systematically and logically than empirically. There is a need for a well-coordinated global initiative comparable to the Human Genome Project to achieve this goal in the near future.

Entities:  

Keywords:  Cell therapy; Embryonic stem cells; Fibroblasts; Gene therapy; Hepatocyte like cells; Hepatocyte transplantation; Induced pluripotent stem cells; Inherited/genetic liver disease; Telomere/telomerase; Trans differentiation; differentiation; i-Heps

Mesh:

Substances:

Year:  2015        PMID: 26074681      PMCID: PMC4458753          DOI: 10.3748/wjg.v21.i21.6427

Source DB:  PubMed          Journal:  World J Gastroenterol        ISSN: 1007-9327            Impact factor:   5.742


  62 in total

1.  Hepatocyte transplantation as a treatment for glycogen storage disease type 1a.

Authors:  Maurizio Muraca; Giorgio Gerunda; Daniele Neri; Maria-Teresa Vilei; Anna Granato; Paolo Feltracco; Muzio Meroni; Gianpiero Giron; Alberto B Burlina
Journal:  Lancet       Date:  2002-01-26       Impact factor: 79.321

2.  Induced pluripotent stem cell-derived hepatocytes have the functional and proliferative capabilities needed for liver regeneration in mice.

Authors:  Silvia Espejel; Garrett R Roll; K John McLaughlin; Andrew Y Lee; Jenny Y Zhang; Diana J Laird; Keisuke Okita; Shinya Yamanaka; Holger Willenbring
Journal:  J Clin Invest       Date:  2010-08-25       Impact factor: 14.808

3.  Highly efficient generation of human hepatocyte-like cells from induced pluripotent stem cells.

Authors:  Karim Si-Tayeb; Fallon K Noto; Masato Nagaoka; Jixuan Li; Michele A Battle; Christine Duris; Paula E North; Stephen Dalton; Stephen A Duncan
Journal:  Hepatology       Date:  2010-01       Impact factor: 17.425

4.  Generation of hybrid hepatocytes by cell fusion from monkey embryoid body cells in the injured mouse liver.

Authors:  Kentaro Okamura; Kinji Asahina; Hiroaki Fujimori; Rie Ozeki; Keiko Shimizu-Saito; Yujiro Tanaka; Kenichi Teramoto; Shigeki Arii; Kozo Takase; Miho Kataoka; Yoshinori Soeno; Chise Tateno; Katsutoshi Yoshizato; Hirobumi Teraoka
Journal:  Histochem Cell Biol       Date:  2005-09-30       Impact factor: 4.304

5.  Efficient generation of hepatocyte-like cells from human induced pluripotent stem cells.

Authors:  Zhihua Song; Jun Cai; Yanxia Liu; Dongxin Zhao; Jun Yong; Shuguang Duo; Xijun Song; Yushan Guo; Yang Zhao; Han Qin; Xiaolei Yin; Chen Wu; Jie Che; Shichun Lu; Mingxiao Ding; Hongkui Deng
Journal:  Cell Res       Date:  2009-09-08       Impact factor: 25.617

6.  Direct reprogramming of human fibroblasts to functional and expandable hepatocytes.

Authors:  Pengyu Huang; Ludi Zhang; Yimeng Gao; Zhiying He; Dan Yao; Zhitao Wu; Jin Cen; Xiaotao Chen; Changcheng Liu; Yiping Hu; Dongmei Lai; Zhenlei Hu; Li Chen; Ying Zhang; Xin Cheng; Xiaojun Ma; Guoyu Pan; Xin Wang; Lijian Hui
Journal:  Cell Stem Cell       Date:  2014-02-27       Impact factor: 24.633

7.  Repopulation of adult and neonatal mice with human hepatocytes: a chimeric animal model.

Authors:  Karl-Dimiter Bissig; Tam T Le; Niels-Bjarne Woods; Inder M Verma
Journal:  Proc Natl Acad Sci U S A       Date:  2007-12-11       Impact factor: 11.205

Review 8.  Genetic and epigenetic variations in iPSCs: potential causes and implications for application.

Authors:  Gaoyang Liang; Yi Zhang
Journal:  Cell Stem Cell       Date:  2013-08-01       Impact factor: 24.633

9.  The reprogrammed pancreatic progenitor-like intermediate state of hepatic cells is more susceptible to pancreatic beta cell differentiation.

Authors:  Qiwei Wang; Hai Wang; Yu Sun; Shi-Wu Li; William Donelan; Lung-Ji Chang; Shouguang Jin; Naohiro Terada; Henrique Cheng; Westley H Reeves; Li-Jun Yang
Journal:  J Cell Sci       Date:  2013-06-07       Impact factor: 5.285

10.  Extended passaging increases the efficiency of neural differentiation from induced pluripotent stem cells.

Authors:  Karl R Koehler; Philippe Tropel; Jonathan W Theile; Takako Kondo; Theodore R Cummins; Stéphane Viville; Eri Hashino
Journal:  BMC Neurosci       Date:  2011-08-10       Impact factor: 3.288

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  4 in total

1.  A small molecule Hedgehog agonist HhAg1.5 mediated reprogramming breaks the quiescence of noninjured liver stem cells for rescuing liver failure.

Authors:  Abhisek Mitra; Jun Yan; Liangfang Zhang; Shulin Li
Journal:  Transl Res       Date:  2018-10-19       Impact factor: 7.012

Review 2.  Current and future therapies for inherited cholestatic liver diseases.

Authors:  Wendy L van der Woerd; Roderick Hj Houwen; Stan Fj van de Graaf
Journal:  World J Gastroenterol       Date:  2017-02-07       Impact factor: 5.742

3.  Cloning of human ABCB11 gene in E. coli required the removal of an intragenic Pribnow-Schaller Box before it's Insertion into genomic safe harbor AAVS1 site using CRISPR-Cas9.

Authors:  Nisha Vats; Madhusudana Girija Sanal; Senthil Kumar Venugopal; Pankaj Taneja; Shiv Kumar Sarin
Journal:  F1000Res       Date:  2020-12-23

Review 4.  Urine-derived cells for human cell therapy.

Authors:  Nimshitha Pavathuparambil Abdul Manaph; Mohammed Al-Hawwas; Larisa Bobrovskaya; Patrick T Coates; Xin-Fu Zhou
Journal:  Stem Cell Res Ther       Date:  2018-07-11       Impact factor: 6.832

  4 in total

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