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
收藏
页数:8
相关论文
共 50 条
  • [21] Generation of immunosuppressive iPSC-derived stromal cells for tissue regeneration
    Scharler, C.
    Peking, P.
    Ketterl, N.
    Hochreiter, A.
    Juerchott, K.
    Brachtl, G.
    Wimmer, M.
    Hochmann, S.
    Wolf, M.
    Schallmoser, K.
    Volk, H. D.
    Strunk, D.
    HUMAN GENE THERAPY, 2018, 29 (12) : A56 - A56
  • [22] Studying tissue macrophages in vitro: are iPSC-derived cells the answer?
    Lee, Christopher Z. W.
    Kozaki, Tatsuya
    Ginhoux, Florent
    NATURE REVIEWS IMMUNOLOGY, 2018, 18 (11) : 716 - 725
  • [23] Modeling Alzheimer's disease with iPSC-derived brain cells
    Penney, Jay
    Ralvenius, William T.
    Tsai, Li-Huei
    MOLECULAR PSYCHIATRY, 2020, 25 (01) : 148 - 167
  • [24] iPSC-Derived Airway Epithelial Cells: Progress, Promise, and Challenges
    Yu, Fenggang
    Liu, Fei
    Liang, Xiaohua
    Duan, Linwei
    Li, Qiongqiong
    Pan, Ge
    Ma, Chengyao
    Liu, Minmin
    Li, Mingyue
    Wang, Peng
    Zhao, Xuening
    STEM CELLS, 2023, 41 (01) : 1 - 10
  • [25] Modeling CLN6 with IPSC-derived neural cells
    Pierson, Tyler Mark
    Otero, Maria Gabriella
    Nonis, David Fabian
    Kim, Jaemin
    MOLECULAR GENETICS AND METABOLISM, 2019, 126 (02) : S118 - S118
  • [26] Applications of iPSC-derived beta cells from patients with diabetes
    Maxwell, Kristina G.
    Millman, Jeffrey R.
    CELL REPORTS MEDICINE, 2021, 2 (04)
  • [27] Modeling Alzheimer’s disease with iPSC-derived brain cells
    Jay Penney
    William T. Ralvenius
    Li-Huei Tsai
    Molecular Psychiatry, 2020, 25 : 148 - 167
  • [28] iPSC-derived EPO-producing cells rescue anaemia
    Allison, Susan J.
    NATURE REVIEWS NEPHROLOGY, 2017, 13 (12) : 722 - 722
  • [29] iPSC-derived EPO-producing cells rescue anaemia
    Susan J. Allison
    Nature Reviews Nephrology, 2017, 13 : 722 - 722
  • [30] IPSC-derived CAR-NK cells for cancer immunotherapy
    Lin, Xiaotong
    Sun, Yao
    Dong, Xin
    Liu, Zishen
    Sugimura, Ryohichi
    Xie, Guozhu
    BIOMEDICINE & PHARMACOTHERAPY, 2023, 165