生物
离体
血小板
脐带血
川地34
分子生物学
干细胞
免疫学
细胞生物学
体内
遗传学
作者
Takuya Matsunaga,Ikuta Tanaka,Masayoshi Kobune,Yutaka Kawano,Maki Tanaka,Kageaki Kuribayashi,Satoshi Iyama,Tsutomu Sato,Yasushi Sato,Rishu Takimoto,Tetsuji Takayama,Junji Kato,Takafumi Ninomiya,Hirofumi Hamada,Yoshiro Niitsu
出处
期刊:Stem Cells
[Oxford University Press]
日期:2006-09-08
卷期号:24 (12): 2877-2887
被引量:128
标识
DOI:10.1634/stemcells.2006-0309
摘要
In the present investigation, we generated platelets (PLTs) from cord blood (CB) CD34(+) cells using a three-phase culture system. We first cultured 500 CB CD34(+) cells on telomerase gene-transduced human stromal cells (hTERT stroma) in serum-free medium supplemented with stem cell factor (SCF), Flt-3/Flk-2 ligand (FL), and thrombopoietin (TPO) for 14 days. We then transferred the cells to hTERT stroma and cultured for another 14 days with fresh medium containing interleukin-11 (IL-11) in addition to the original cytokine cocktail. Subsequently, we cultured the cells in a liquid culture medium containing SCF, FL, TPO, and IL-11 for another 5 days to recover PLT fractions from the supernatant, which were then gel-filtered to purify the PLTs. The calculated yield of PLTs from 1.0 unit of CB (5 x 10(6) CD34(+) cells) was 1.26 x 10(11) - 1.68 x 10(11) PLTs. These numbers of PLTs are equivalent to 2.5-3.4 units of random donor-derived PLTs or 2/5-6/10 of single-apheresis PLTs. The CB-derived PLTs exhibited features quite similar to those from peripheral blood in morphology, as revealed by electron micrographs, and in function, as revealed by fibrinogen/ADP aggregation, with the appearance of P-selectin and activated glycoprotein IIb-IIIa antigens. Thus, this culture system may be applicable for large-scale generation of PLTs for future clinical use.
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