| Literature DB >> 24529595 |
Sou Nakamura1, Naoya Takayama1, Shinji Hirata1, Hideya Seo1, Hiroshi Endo1, Kiyosumi Ochi1, Ken-ichi Fujita1, Tomo Koike1, Ken-ichi Harimoto1, Takeaki Dohda1, Akira Watanabe2, Keisuke Okita2, Nobuyasu Takahashi3, Akira Sawaguchi3, Shinya Yamanaka2, Hiromitsu Nakauchi4, Satoshi Nishimura5, Koji Eto6.
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.Entities:
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Year: 2014 PMID: 24529595 DOI: 10.1016/j.stem.2014.01.011
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633