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Multifaceted Characterization of Human Embryonic Stem Cell-Derived Mesenchymal Stem/Stromal Cells Revealed Amelioration of Acute Liver Injury in NOD-SCID Mice
by
Zhang, Leisheng
, Zhang, Youlai
, He, Ying
, Jiang, Zhenyu
, Deng, Rufei
, Zou, Lijin
, Zeng, Yuanlin
in
5-aza-2'-deoxycytidine
/ Animals
/ Bioinformatics
/ Cell Differentiation
/ Embryo cells
/ Flow cytometry
/ Gene expression
/ Hepatocytes
/ Human Embryonic Stem Cells
/ Humans
/ Liver
/ Liver transplantation
/ Mesenchymal Stem Cell Transplantation - methods
/ Mesenchymal Stem Cells
/ Mice
/ Mice, Inbred NOD
/ Mice, SCID
/ Polymerase chain reaction
/ Principal components analysis
/ Reverse transcription
/ Stem cells
/ Stromal cells
/ Transcriptomics
2024
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Multifaceted Characterization of Human Embryonic Stem Cell-Derived Mesenchymal Stem/Stromal Cells Revealed Amelioration of Acute Liver Injury in NOD-SCID Mice
by
Zhang, Leisheng
, Zhang, Youlai
, He, Ying
, Jiang, Zhenyu
, Deng, Rufei
, Zou, Lijin
, Zeng, Yuanlin
in
5-aza-2'-deoxycytidine
/ Animals
/ Bioinformatics
/ Cell Differentiation
/ Embryo cells
/ Flow cytometry
/ Gene expression
/ Hepatocytes
/ Human Embryonic Stem Cells
/ Humans
/ Liver
/ Liver transplantation
/ Mesenchymal Stem Cell Transplantation - methods
/ Mesenchymal Stem Cells
/ Mice
/ Mice, Inbred NOD
/ Mice, SCID
/ Polymerase chain reaction
/ Principal components analysis
/ Reverse transcription
/ Stem cells
/ Stromal cells
/ Transcriptomics
2024
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Multifaceted Characterization of Human Embryonic Stem Cell-Derived Mesenchymal Stem/Stromal Cells Revealed Amelioration of Acute Liver Injury in NOD-SCID Mice
by
Zhang, Leisheng
, Zhang, Youlai
, He, Ying
, Jiang, Zhenyu
, Deng, Rufei
, Zou, Lijin
, Zeng, Yuanlin
in
5-aza-2'-deoxycytidine
/ Animals
/ Bioinformatics
/ Cell Differentiation
/ Embryo cells
/ Flow cytometry
/ Gene expression
/ Hepatocytes
/ Human Embryonic Stem Cells
/ Humans
/ Liver
/ Liver transplantation
/ Mesenchymal Stem Cell Transplantation - methods
/ Mesenchymal Stem Cells
/ Mice
/ Mice, Inbred NOD
/ Mice, SCID
/ Polymerase chain reaction
/ Principal components analysis
/ Reverse transcription
/ Stem cells
/ Stromal cells
/ Transcriptomics
2024
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Multifaceted Characterization of Human Embryonic Stem Cell-Derived Mesenchymal Stem/Stromal Cells Revealed Amelioration of Acute Liver Injury in NOD-SCID Mice
Journal Article
Multifaceted Characterization of Human Embryonic Stem Cell-Derived Mesenchymal Stem/Stromal Cells Revealed Amelioration of Acute Liver Injury in NOD-SCID Mice
2024
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Overview
Human embryonic stem cells (hESCs) are advantaged sources for large-scale and homogeneous mesenchymal stem/stromal cells (MSCs) generation. However, due to the limitations in high-efficiency procedures for hESC-MSCs induction, the systematic and detailed information of mesengenesis and early MSC development are largely obscure. In this study, we took advantage of the well-established twist-related protein 1 (TWIST1)-overexpressing hESCs and two small molecular cocktails (CHIR99021, decitabine) for high-efficient MSC induction. To assess the multidimensional biological and transcriptomic characteristics, we turned to cellular and molecular methods, such as flow cytometry (FCM), quantitative reverse transcription–polymerase chain reaction (qRT-PCR), in vitro tri-lineage differentiation, cytokine secretion analysis, in vivo transplantation for acute liver injury (ALI) management, and bioinformatics analyses (eg, gene ontology–biological processes [GO-BP], Kyoto Encyclopedia of Genes and Genomes [KEGG], HeatMap, and principal component analysis [PCA]). By combining TWIST1 overexpression (denoted as T) and the indicated small molecular cocktails (denoted as S), hESCs high-efficiently differentiated into MSCs (denoted as TS-MSCs, induced by T and S combination) within 2 weeks. TS-MSCs satisfied the criteria for MSC definition and revealed comparable tri-lineage differentiation potential and ameliorative efficacy upon ALI mice. According to RNA-sequencing (SEQ) analysis, we originally illuminated the gradual variations in gene expression pattern and the concomitant biofunctions of the programmed hESC-MSCs. Overall, our data indicated the feasibility of high-efficient generation of hESC-MSCs by TWIST1 and cocktail-based programming. The generated hESC-MSCs revealed multifaceted in vivo and in vitro biofunctions as adult BM-MSCs, which collectively suggested promising prospects in ALI management in future.
Publisher
SAGE Publications,Sage Publications Ltd,SAGE Publishing
Subject
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