iPSC-derived cells for whole liver bioengineering

被引:0
|
作者
Telles-Silva, Kayque Alves [1 ,2 ]
Pacheco, Lara [1 ]
Chianca, Fernanda [1 ]
Komatsu, Sabrina [1 ]
Chiovatto, Caroline [1 ]
Zatz, Mayana [1 ]
Goulart, Ernesto [1 ]
机构
[1] Univ Sao Paulo, Inst Biosci, Human Genome & Stem Cell Res Ctr HUG CEL, Sao Paulo, Brazil
[2] Univ Calif San Francisco, Small Mol Discovery Ctr, Dept Pharmaceut Chem, Genentech Hall, San Francisco, CA USA
基金
巴西圣保罗研究基金会;
关键词
liver; bioengineering; human induced pluripotent stem cells; decellularization; bioprinting; MODELS;
D O I
10.3389/fbioe.2024.1338762
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Liver bioengineering stands as a prominent alternative to conventional hepatic transplantation. Through liver decellularization and/or bioprinting, researchers can generate acellular scaffolds to overcome immune rejection, genetic manipulation, and ethical concerns that often accompany traditional transplantation methods, in vivo regeneration, and xenotransplantation. Hepatic cell lines derived from induced pluripotent stem cells (iPSCs) can repopulate decellularized and bioprinted scaffolds, producing an increasingly functional organ potentially suitable for autologous use. In this mini-review, we overview recent advancements in vitro hepatocyte differentiation protocols, shedding light on their pivotal role in liver recellularization and bioprinting, thereby offering a novel source for hepatic transplantation. Finally, we identify future directions for liver bioengineering research that may allow the implementation of these systems for diverse applications, including drug screening and liver disease modeling. Schematic representation of in vitro differentiation protocols (A) and bioengineering applications (B). hiPSC = human induced pluripotent stem cell. (Created with BioRender.com.
引用
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页数:8
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