Analysis of differentially expressed genes among human hair follicle-derived iPSCs, induced hepatocyte-like cells, and primary hepatocytes

被引:9
|
作者
Xu, Ziran [1 ]
He, Xia [1 ]
Shi, Xu [2 ]
Xia, Yuhan [1 ]
Liu, Xiaomei [3 ]
Wu, Haitao [1 ]
Li, Pengdong [1 ]
Zhang, Hongyu [1 ]
Yin, Weisi [1 ]
Du, Xiubo [4 ]
Li, Lisha [1 ]
Li, Yulin [1 ]
机构
[1] Jilin Univ, Norman Bethune Coll Med, Key Lab Pathobiol, Minist Educ, Changchun 130021, Jilin, Peoples R China
[2] Jilin Univ, Cent Lab, Hosp 1, Changchun 130021, Jilin, Peoples R China
[3] Beijing Hosp Tradit Chinese Med, Beijing 100069, Peoples R China
[4] Shenzhen Univ, Coll Life Sci & Oceanog, Shenzhen Key Lab Microbial Genet Engn, Shenzhen, Peoples R China
基金
中国国家自然科学基金;
关键词
Induced pluripotent stem cells; Stem cell differentiation; Hepatocyte-like cells; Differentially expressed genes; Microarray analysis; HUMAN EMBRYONIC STEM; DEFINITIVE ENDODERM; LIVER-DISEASE; IN-VITRO; PROLIFERATION; METASTASIS; GENERATION; SIGNATURES; ONTOLOGY; PROTEIN;
D O I
10.1186/s13287-018-0940-z
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Background: Differentiation of human induced pluripotent stem cells (hiPSCs) into hepatocytes has important clinical significance in providing a new stem cell source for cell therapy of terminal liver disease. The differential gene expression analysis of hiPSCs, induced hepatocyte-like cells (HLCs), and primary human hepatocytes (PHHs) provides valuable information for optimization of an induction scheme and exploration of differentiation mechanisms. Methods: Human hair follicle-derived iPSCs (hHF-iPSCs) were induced in vitro by mimicking the environment of a developing liver for 19 days. Expression of specific proteins was determined by immunofluorescence staining; the function of HLCs in storage and metabolism was identified by detecting periodic acid-Schiff, indocyanine green, and low-density lipoprotein. Based on the transcriptomics data, the differential gene expression profiles of hHF-iPSCs, HLCs, and PHHs were analyzed by Gene Ontology, Kyoto Encyclopedia of Genes and Genomes pathway, FunRich, and network analysis methods. Results: HLCs were able to express albumin (ALB), alpha-fetoprotein, CYP3A4, and CYP7A1, and exhibited matured liver cell functions such as glycogen synthesis and storage. Complement and coagulation cascades and metabolic pathways ranked top in the downregulated list of HLCs/PHHs, while the cell cycle ranked top in the upregulated list of HLCs/PHHs. In the protein-protein interaction network, according to the degree rankings, TOP2A, CDK1, etc. were the important upregulated differentially expressed genes (DEGs), while ALB, ACACB, etc. were the major downregulated DEGs in HLCs/ PHHs; the module analysis indicated that CDCA8, AURKB, and AURKA were the top upregulated DEGs in HLCs/PHHs. Conclusions: We presented the differences in gene expression among hHF-iPSCs, HLCs, and PHHs through transcriptome array data and provided new ideas for the optimization of induction.
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页数:15
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