-
Je něco špatně v tomto záznamu ?
Technological advancements for the development of stem cell-based models for hepatotoxicity testing
A. Natale, K. Vanmol, A. Arslan, S. Van Vlierberghe, P. Dubruel, J. Van Erps, H. Thienpont, M. Buzgo, J. Boeckmans, J. De Kock, T. Vanhaecke, V. Rogiers, RM. Rodrigues,
Jazyk angličtina Země Německo
Typ dokumentu časopisecké články, práce podpořená grantem, přehledy
- MeSH
- alternativy testů na zvířatech metody MeSH
- buněčná diferenciace účinky léků MeSH
- buněčné kultury MeSH
- hepatocyty cytologie účinky léků MeSH
- játra účinky léků MeSH
- kmenové buňky cytologie účinky léků MeSH
- lékové postižení jater etiologie MeSH
- lidé MeSH
- xenobiotika toxicita MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- přehledy MeSH
Stem cells are characterized by their self-renewal capacity and their ability to differentiate into multiple cell types of the human body. Using directed differentiation strategies, stem cells can now be converted into hepatocyte-like cells (HLCs) and therefore, represent a unique cell source for toxicological applications in vitro. However, the acquired hepatic functionality of stem cell-derived HLCs is still significantly inferior to primary human hepatocytes. One of the main reasons for this is that most in vitro models use traditional two-dimensional (2D) setups where the flat substrata cannot properly mimic the physiology of the human liver. Therefore, 2D-setups are progressively being replaced by more advanced culture systems, which attempt to replicate the natural liver microenvironment, in which stem cells can better differentiate towards HLCs. This review highlights the most recent cell culture systems, including scaffold-free and scaffold-based three-dimensional (3D) technologies and microfluidics that can be employed for culture and hepatic differentiation of stem cells intended for hepatotoxicity testing. These methodologies have shown to improve in vitro liver cell functionality according to the in vivo liver physiology and allow to establish stem cell-based hepatic in vitro platforms for the accurate evaluation of xenobiotics.
Brussels Photonics Centre of Macromolecular Chemistry Ghent University Ghent Belgium
Brussels Photonics Vrije Universiteit Brussel and Flanders Make Brussels Belgium
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc20025785
- 003
- CZ-PrNML
- 005
- 20201222160405.0
- 007
- ta
- 008
- 201125s2019 gw f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1007/s00204-019-02465-y $2 doi
- 035 __
- $a (PubMed)31037322
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a gw
- 100 1_
- $a Natale, Alessandra $u Department of In Vitro Toxicology and Dermato-Cosmetology (IVTD), Vrije Universiteit Brussel, Brussels, Belgium.
- 245 10
- $a Technological advancements for the development of stem cell-based models for hepatotoxicity testing / $c A. Natale, K. Vanmol, A. Arslan, S. Van Vlierberghe, P. Dubruel, J. Van Erps, H. Thienpont, M. Buzgo, J. Boeckmans, J. De Kock, T. Vanhaecke, V. Rogiers, RM. Rodrigues,
- 520 9_
- $a Stem cells are characterized by their self-renewal capacity and their ability to differentiate into multiple cell types of the human body. Using directed differentiation strategies, stem cells can now be converted into hepatocyte-like cells (HLCs) and therefore, represent a unique cell source for toxicological applications in vitro. However, the acquired hepatic functionality of stem cell-derived HLCs is still significantly inferior to primary human hepatocytes. One of the main reasons for this is that most in vitro models use traditional two-dimensional (2D) setups where the flat substrata cannot properly mimic the physiology of the human liver. Therefore, 2D-setups are progressively being replaced by more advanced culture systems, which attempt to replicate the natural liver microenvironment, in which stem cells can better differentiate towards HLCs. This review highlights the most recent cell culture systems, including scaffold-free and scaffold-based three-dimensional (3D) technologies and microfluidics that can be employed for culture and hepatic differentiation of stem cells intended for hepatotoxicity testing. These methodologies have shown to improve in vitro liver cell functionality according to the in vivo liver physiology and allow to establish stem cell-based hepatic in vitro platforms for the accurate evaluation of xenobiotics.
- 650 _2
- $a alternativy testů na zvířatech $x metody $7 D000826
- 650 _2
- $a buněčné kultury $7 D018929
- 650 _2
- $a buněčná diferenciace $x účinky léků $7 D002454
- 650 _2
- $a lékové postižení jater $x etiologie $7 D056486
- 650 _2
- $a hepatocyty $x cytologie $x účinky léků $7 D022781
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a játra $x účinky léků $7 D008099
- 650 _2
- $a kmenové buňky $x cytologie $x účinky léků $7 D013234
- 650 _2
- $a xenobiotika $x toxicita $7 D015262
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 655 _2
- $a přehledy $7 D016454
- 700 1_
- $a Vanmol, Koen $u Brussels Photonics (B-PHOT), Vrije Universiteit Brussel and Flanders Make, Brussels, Belgium.
- 700 1_
- $a Arslan, Aysu $u Polymer Chemistry and Biomaterials Group (PBM), Centre of Macromolecular Chemistry, Ghent University, Ghent, Belgium.
- 700 1_
- $a Van Vlierberghe, Sandra $u Brussels Photonics (B-PHOT), Vrije Universiteit Brussel and Flanders Make, Brussels, Belgium. Polymer Chemistry and Biomaterials Group (PBM), Centre of Macromolecular Chemistry, Ghent University, Ghent, Belgium.
- 700 1_
- $a Dubruel, Peter $u Polymer Chemistry and Biomaterials Group (PBM), Centre of Macromolecular Chemistry, Ghent University, Ghent, Belgium.
- 700 1_
- $a Van Erps, Jürgen $u Brussels Photonics (B-PHOT), Vrije Universiteit Brussel and Flanders Make, Brussels, Belgium.
- 700 1_
- $a Thienpont, Hugo $u Brussels Photonics (B-PHOT), Vrije Universiteit Brussel and Flanders Make, Brussels, Belgium.
- 700 1_
- $a Buzgo, Matij $u Inocure, Prague, Czech Republic.
- 700 1_
- $a Boeckmans, Joost $u Department of In Vitro Toxicology and Dermato-Cosmetology (IVTD), Vrije Universiteit Brussel, Brussels, Belgium.
- 700 1_
- $a De Kock, Joery $u Department of In Vitro Toxicology and Dermato-Cosmetology (IVTD), Vrije Universiteit Brussel, Brussels, Belgium.
- 700 1_
- $a Vanhaecke, Tamara $u Department of In Vitro Toxicology and Dermato-Cosmetology (IVTD), Vrije Universiteit Brussel, Brussels, Belgium.
- 700 1_
- $a Rogiers, Vera $u Department of In Vitro Toxicology and Dermato-Cosmetology (IVTD), Vrije Universiteit Brussel, Brussels, Belgium.
- 700 1_
- $a Rodrigues, Robim M $u Department of In Vitro Toxicology and Dermato-Cosmetology (IVTD), Vrije Universiteit Brussel, Brussels, Belgium. robim.marcelino.rodrigues@vub.be.
- 773 0_
- $w MED00009265 $t Archives of toxicology $x 1432-0738 $g Roč. 93, č. 7 (2019), s. 1789-1805
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/31037322 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20201125 $b ABA008
- 991 __
- $a 20201222160401 $b ABA008
- 999 __
- $a ok $b bmc $g 1599930 $s 1116471
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2019 $b 93 $c 7 $d 1789-1805 $e 20190429 $i 1432-0738 $m Archives of toxicology $n Arch Toxicol $x MED00009265
- LZP __
- $a Pubmed-20201125