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源自灵长类胚胎干细胞的长期体外造血作用。

Long-lasting in vitro hematopoiesis derived from primate embryonic stem cells.

作者信息

Hiroyama Takashi, Miharada Kenichi, Aoki Naoko, Fujioka Tsuyoshi, Sudo Kazuhiro, Danjo Inaho, Nagasawa Toshiro, Nakamura Yukio

机构信息

Cell Engineering Division, RIKEN BioResource Center, Tsukuba, Ibaraki, Japan.

出版信息

Exp Hematol. 2006 Jun;34(6):760-9. doi: 10.1016/j.exphem.2006.03.004.

Abstract

OBJECTIVE

Induction of hematopoietic cells from human embryonic stem (ES) cells has been reported recently. However, before cells derived from human ES cells can be used in the clinic, preclinical studies using these cells in experimental primates will be necessary. Therefore, we attempted to establish a method to induce hematopoietic cells robustly and abundantly from primate ES cells.

METHODS

A primate ES cell line, CMK-6, derived from the cynomolgus monkey was used in this study. We adapted a method to induce hematopoiesis from CMK-6 cells on feeder cells, and tested the effectiveness of three kinds of feeder cell lines (OP9, C2C12, and C3H10T1/2). In addition, we tested the effect of vascular endothelial growth factor (VEGF) and insulin-like growth factor-II (IGF-II) on hematopoiesis induction from CMK-6 cells.

RESULTS

VEGF and IGF-II showed an extremely strong synergistic effect to induce hematopoiesis from CMK-6 cells. C3H10T1/2 cells proved to be very useful for the induction of hematopoiesis from CMK-6 cells, and the production of blood cells on C3H10T1/2 cells has been maintained as long as 5 months. During this long period, ES cell derivatives continuously produced mature blood cells, including terminally differentiated cells.

CONCLUSION

We have developed an original method to produce enriched blood cells abundantly from primate ES cells for an extremely long period. This method may represent a good in vitro model for studying primate hematopoiesis and related diseases. Furthermore, our method may be useful for preclinical studies of transfusion therapy using blood cells derived from ES cells in experimental primate systems.

摘要

目的

最近有报道称可从人胚胎干细胞(ES细胞)诱导生成造血细胞。然而,在源自人ES细胞的细胞能够用于临床之前,有必要在实验灵长类动物中对这些细胞进行临床前研究。因此,我们尝试建立一种从灵长类ES细胞高效且大量诱导造血细胞的方法。

方法

本研究使用了源自食蟹猴的灵长类ES细胞系CMK-6。我们采用了一种在饲养细胞上从CMK-6细胞诱导造血的方法,并测试了三种饲养细胞系(OP9、C2C12和C3H10T1/2)的有效性。此外,我们测试了血管内皮生长因子(VEGF)和胰岛素样生长因子-II(IGF-II)对从CMK-6细胞诱导造血的影响。

结果

VEGF和IGF-II对从CMK-6细胞诱导造血显示出极强的协同作用。事实证明,C3H10T1/2细胞对于从CMK-6细胞诱导造血非常有用,并且在C3H10T1/2细胞上血细胞的生成已维持了长达5个月。在这一漫长时期内,ES细胞衍生物持续产生成熟血细胞,包括终末分化细胞。

结论

我们开发了一种原创方法,可在极长时期内从灵长类ES细胞大量产生富集的血细胞。该方法可能是研究灵长类造血及相关疾病的良好体外模型。此外,我们的方法可能有助于在实验灵长类动物系统中对使用源自ES细胞的血细胞进行输血治疗的临床前研究。

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