Department of Clinical Application, Center for iPS Cell Research and Application (CiRA), Kyoto University, 606-8507, Japan.
Department of Reprogramming Science, CiRA, Kyoto University, 606-8507, Japan.
Cell Stem Cell. 2014 Apr 3;14(4):535-48. doi: 10.1016/j.stem.2014.01.011. Epub 2014 Feb 13.
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.
供者依赖性血小板供应常常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)中获得功能性血小板的临床适用策略。该方法涉及通过过表达 BMI1 和 BCL-XL 从 PSC 来源的造血祖细胞中建立稳定的永生化巨核细胞祖细胞系(imMKCL),分别抑制衰老和细胞凋亡,以及限制过表达 c-MYC 以促进增殖。由此产生的 imMKCL 可以在培养中长期(4-5 个月)扩增,甚至在冷冻保存后也可以扩增。在生长中的 imMKCL 中停止过表达 c-MYC、BMI1 和 BCL-XL,导致基于一系列体外和体内测定,产生具有与天然血小板相当功能的 CD42b(+)血小板。强大的扩增能力和高效的血小板生成能力意味着,适当选择的 imMKCL 克隆代表了一种用于临床应用的潜在取之不尽的 hPSC 来源血小板的来源。