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首页> 外文期刊>Cell stem cell >Expandable Megakaryocyte Cell Lines Enable Clinically Applicable Generation of Platelets from Human Induced Pluripotent Stem Cells
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Expandable Megakaryocyte Cell Lines Enable Clinically Applicable Generation of Platelets from Human Induced Pluripotent Stem Cells

机译:可扩展的巨核细胞系能够从人诱导的多能干细胞中临床适用的血小板

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摘要

The donor-dependent supply of platelets is frequently insufficient to meet transfusion needs. To address this issue, we developed a clinically applicable strategy for the derivation of functional platelets from human pluripotent stem cells (PSCs). This approach involves the establishment of stable immortalized megakaryocyte progenitor cell lines (imMKCLs) from PSC-derived hematopoietic progenitors through the overexpression of BMI1 and BCL-XL to respectively suppress senescence and apoptosis and the constrained overexpression of c-MYC to promote proliferation. The resulting imMKCLs can be expanded in culture over extended periods (4-5 months), even after cryopreservation. Halting the overexpression of c-MYC, BMI1, and BCL-XL in growing imMKCLs led to the production of CD42b+ platelets with functionality comparable to that of native platelets on the basis of a range of assays in vitro and in vivo. The combination of robust expansion capacity and efficient platelet production means that appropriately selected imMKCL clones represent a potentially inexhaustible source of hPSC-derived platelets for clinical application.
机译:供体依赖的血小板供应往往不足以满足输血需求。为了解决这个问题,我们开发了一种从人类多能干细胞(PSC)衍生功能性血小板的临床应用策略。这种方法包括通过BMI1和BCL-XL的过度表达分别抑制衰老和凋亡,以及c-MYC的限制性过度表达促进增殖,从PSC衍生的造血祖细胞建立稳定的永生化巨核细胞祖细胞系(IMMKCL)。由此产生的imMKCLs可以在培养物中长时间(4-5个月)扩增,即使在冷冻保存后也是如此。在体外和体内的一系列分析基础上,停止生长的IMMKCl中c-MYC、BMI1和BCL-XL的过度表达,可产生功能与天然血小板相当的CD42b+血小板。强大的扩增能力和高效的血小板生产相结合意味着,适当选择的imMKCL克隆代表了临床应用中潜在的取之不尽的hPSC衍生血小板来源。

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