Regulated differentiation of stem cells into an artificial 3D liver as a transplantable source

被引:4
作者
Chen, Feng [1 ]
Wang, Hua [2 ]
Xiao, Jia [3 ]
机构
[1] Shenzhen Third Peoples Hosp, Natl Key Disciplines Infect Dis, Shenzhen, Peoples R China
[2] Anhui Med Univ, Affiliated Hosp 1, Dept Oncol, Inst Liver Dis, Hefei, Peoples R China
[3] Jinan Univ, Clin Med Res Inst, Affiliated Hosp 1, 613 Huangpu Ave, Guangzhou 510632, Peoples R China
基金
中国国家自然科学基金;
关键词
Stem cells; Differentiation; Decellularized matrix; Natural macromolecules; Synthetic polymers; HEPATOCYTE-LIKE CELLS; SINUSOIDAL ENDOTHELIAL-CELLS; HEPATIC STELLATE CELLS; PLLA NANOFIBROUS SCAFFOLDS; LACTIC ACID SCAFFOLDS; ENGINEERED LIVER; PROGENITOR CELLS; KUPFFER CELLS; CULTURE; GENERATION;
D O I
10.3350/cmh.2019.0022n
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
End-stage liver disease is one of the leading causes of death around the world. Since insufficient sources of transplantable liver and possible immune rejection severely hinder the wide application of conventional liver transplantation therapy, artificial three-dimensional (3D) liver culture and assembly from stem cells have become a new hope for patients with end-stage liver diseases, such as cirrhosis and liver cancer. However, the induced differentiation of single-layer or 3D-structured hepatocytes from stern cells cannot physiologically support essential liver functions due to the lack of formation of blood vessels, immune regulation, storage of vitamins, and other vital hepatic activities. Thus, there is emerging evidence showing that 3D organogenesis of artificial vascularized liver tissue from combined hepatic cell types derived from differentiated stem cells is practical for the treatment of end-stage liver diseases. The optimization of novel biomaterials, such as decellularized matrices and natural macromolecules, also strongly supports the organogenesis of 3D tissue with the desired complex structure. This review summarizes new research updates on novel differentiation protocols of stem cell-derived major hepatic cell types and the application of new supportive biomaterials. Future biological and clinical challenges of this concept are also discussed.
引用
收藏
页码:163 / 179
页数:17
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