Multifaceted Characterization of Human Embryonic Stem Cell-Derived Mesenchymal Stem/Stromal Cells Revealed Amelioration of Acute Liver Injury in NOD-SCID Mice.

IF 3.2 4区 医学 Q3 CELL & TISSUE ENGINEERING Cell Transplantation Pub Date : 2024-01-01 DOI:10.1177/09636897231218383
Youlai Zhang, Ying He, Rufei Deng, Zhenyu Jiang, Leisheng Zhang, Yuanlin Zeng, Lijin Zou
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Abstract

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.

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人胚胎干细胞衍生间充质干细胞/基质细胞的多方面特征揭示了对 NOD-SCID 小鼠急性肝损伤的改善作用
人类胚胎干细胞(hESCs)是大规模均匀生成间充质干细胞/间质细胞(MSCs)的有利来源。然而,由于高效的 hESC-间充质干细胞诱导程序的局限性,间充质干细胞的系统性和早期发育的详细信息非常模糊。在本研究中,我们利用已被证实的扭转相关蛋白 1(TWIST1)表达的 hESCs 和两种小分子鸡尾酒(CHIR99021、地西他滨)进行高效间充质干细胞诱导。为了评估其多维生物学和转录组学特征,我们采用了细胞和分子方法,如流式细胞术(FCM)、定量反转录聚合酶链反应(qRT-PCR)、体外三系分化、细胞因子分泌分析、基因组学分析等、细胞因子分泌分析、用于急性肝损伤(ALI)管理的体内移植以及生物信息学分析(如基因本体-生物过程[GO-BP]、京都基因和基因组百科全书[KEGG]、HeatMap 和主成分分析[PCA])。通过结合TWIST1过表达(T)和指定的小分子鸡尾酒(S),hESCs在两周内高效分化成了间充质干细胞(TS-MSCs,由T和S组合诱导)。TS-间充质干细胞符合间充质干细胞的定义标准,并对ALI小鼠具有相似的三系分化潜能和改善疗效。根据 RNA 序列(SEQ)分析,我们初步揭示了程序化 hESC-间充质干细胞基因表达模式的渐变及相应的生物功能。总之,我们的数据表明,通过 TWIST1 和基于鸡尾酒的编程方法高效生成 hESC-间充质干细胞是可行的。所生成的 hESC-间充质干细胞与成体 BM-间充质干细胞一样,具有多方面的体内和体外生物功能,这共同预示着未来在 ALI 治疗中大有可为。
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来源期刊
Cell Transplantation
Cell Transplantation 生物-细胞与组织工程
CiteScore
6.00
自引率
3.00%
发文量
97
审稿时长
6 months
期刊介绍: Cell Transplantation, The Regenerative Medicine Journal is an open access, peer reviewed journal that is published 12 times annually. Cell Transplantation is a multi-disciplinary forum for publication of articles on cell transplantation and its applications to human diseases. Articles focus on a myriad of topics including the physiological, medical, pre-clinical, tissue engineering, stem cell, and device-oriented aspects of the nervous, endocrine, cardiovascular, and endothelial systems, as well as genetically engineered cells. Cell Transplantation also reports on relevant technological advances, clinical studies, and regulatory considerations related to the implantation of cells into the body in order to provide complete coverage of the field.
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