首页> 外文期刊>Cellular reprogramming >Induced Pluripotent Stem Cells Generated from Adult Bone Marrow-Derived Cells of the Nonhuman Primate (Callithrix jacchus) Using a Novel Quad-Cistronic and Excisable Lentiviral Vector
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Induced Pluripotent Stem Cells Generated from Adult Bone Marrow-Derived Cells of the Nonhuman Primate (Callithrix jacchus) Using a Novel Quad-Cistronic and Excisable Lentiviral Vector

机译:诱导的多能干细胞从成年骨髓衍生的非人类灵长类(Callithrix jacchus)的成年骨髓衍生细胞,使用新型的四顺反子和可切除的慢病毒载体

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摘要

Regenerative medicine is in need of solid, large animal models as a link between rodents and humans to evaluate the functionality, immunogenicity, and clinical safety of stem cell–derived cell types. The common marmoset (Callithrix jacchus) is an excellent large animal model, genetically close to humans and readily used worldwide in clinical research. Until now, only two groups showed the generation of induced pluripotent stem cells (iPSCs) from the common marmoset using integrating retroviral vectors. Therefore, we reprogrammed bone marrow–derived mesenchymal cells (MSCs) of adult marmosets in the presence of TAV, SB431542, PD0325901, and ascorbic acid via a novel, excisable lentiviral spleen focus-forming virus (SFFV)-driven quad-cistronic vector system (OCT3/4, KLF4, SOX2, C-MYC). Endogenous pluripotency markers like OCT3/4, KLF4, SOX2, C-MYC, LIN28, NANOG, and strong alkaline phosphatase signals were detected. Exogenous genes were silenced and additionally the cassette was removed with a retroviral Gag precursor system. The cell line could be cultured in absence of leukemia inhibitory factor (LIF) and basic fibroblast growth factor (bFGF) and could be successfully differentiated into embryoid bodies and teratomas with presence of all three germ layers. Directed differentiation generated neural progenitors, megakaryocytes, adipocytes, chondrocytes, and osteogenic cells. Thus, all criteria for fully reprogrammed bone marrow–MSCs of a nonhuman primate with a genetically sophisticated construct could be demonstrated. These cells will be a promising tool for future autologous transplantations.
机译:再生医学需要坚固的大型动物模型作为啮齿动物和人类之间的联系,以评估干细胞衍生细胞类型的功能,免疫原性和临床安全性。普通mar猴(Callithrix jacchus)是一种出色的大型动物模型,在遗传上与人类接近,并已在全球范围内广泛用于临床研究。到目前为止,只有两组显示使用整合的逆转录病毒载体从普通mar猴体内诱导出多能干细胞(iPSC)。因此,我们通过新型,可激发的慢病毒脾聚焦形成病毒(SFFV)驱动的四顺反子向量载体系统,在存在TAV,SB431542,PD0325901和抗坏血酸的情况下,对成年mar猴的骨髓间充质细胞(MSC)进行了重新编程(OCT3 / 4,KLF4,SOX2,C-MYC)。检测到内源性多能性标记物,如OCT3 / 4,KLF4,SOX2,C-MYC,LIN28,NANOG和强碱性磷酸酶信号。使外源基因沉默,并另外用逆转录病毒Gag前体系统除去该盒。该细胞系可以在不存在白血病抑制因子(LIF)和碱性成纤维细胞生长因子(bFGF)的情况下进行培养,并且可以在所有三个胚层均存在的情况下成功分化为胚状体和畸胎瘤。定向分化产生神经祖细胞,巨核细胞,脂肪细胞,软骨细胞和成骨细胞。因此,可以证明具有遗传复杂构造的非人类灵长类动物的完全重编程骨髓-MSC的所有标准。这些细胞将是未来自体移植的有前途的工具。

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