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Scalable Generation of Mesenchymal Stem Cells from Human Embryonic Stem Cells in 3D

机译:从人类胚胎干细胞3D可扩展生成间充质干细胞

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Human embryonic stem cell (hESC) derived mesenchymal stem cells (EMSC) are efficacious in treating a series of autoimmune, inflammatory, and degenerative diseases in animal models. However, all the EMSC derivation methods reported so far rely on two-dimensional (2D) culture systems, which are inefficient, costive and difficult for large-scale production. HESC, as an unlimited source, can be successively propagated in spheroids. Here, we demonstrate that hESC spheroids can directly differentiate into MSC spheroids (EMSCSp) within 20 days in one vessel without passaging and the system is scalable to any desired size. EMSCSp can further differentiate into osteocytes and chondrocytes in spheres or demineralized bone matrix. EMSCSp also retains immune-modulatory effects in vitro and therapeutic effects on two mouse models of colitis after dissociation. Compared to EMSC differentiated in monolayer, EMSCSp-derived cells have faster proliferation and higher yield and develop less apoptosis and slower senescence. Thus, the 3D differentiation system allows simple, cost-effective, and scalable production of high-quality EMSC and subsequently bone and cartilage tissues for therapeutic application.
机译:人类胚胎干细胞(hESC)衍生的间充质干细胞(EMSC)可有效治疗动物模型中的一系列自身免疫,炎性和变性疾病。但是,到目前为止,所有报道的EMSC推导方法都依赖于二维(2D)培养系统,该系统效率低,成本高且难以大规模生产。 HESC作为无限来源,可以以球状体的形式连续传播。在这里,我们证明了hESC球状体可以在20天之内直接在一个容器中分化为MSC球状体(EMSCSp),而无需传代,并且该系统可扩展至任何所需的大小。 EMSCSp可以进一步分化为球形或软化骨基质中的骨细胞和软骨细胞。 EMSCSp还在离体后保留了体外免疫调节作用和对两种结肠炎小鼠模型的治疗作用。与单层分化的EMSC相比,EMSCSp衍生的细胞具有更快的增殖和更高的产量,并具有更少的凋亡和更慢的衰老。因此,该3D分化系统允许简单,经济高效且可扩展地生产高质量的EMSC,然后再生产骨骼和软骨组织以进行治疗。

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