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可膨胀巨核细胞系使人类诱导多能干细胞生成血小板的临床应用成为可能。

Expandable megakaryocyte cell lines enable clinically applicable generation of platelets from human induced pluripotent stem cells.

机构信息

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.

出版信息

Cell Stem Cell. 2014 Apr 3;14(4):535-48. doi: 10.1016/j.stem.2014.01.011. Epub 2014 Feb 13.

Abstract

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.

摘要

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。

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