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人脐血原始造血细胞培养中 GSK-3 抑制剂的特征。

Characterization of a GSK-3 inhibitor in culture of human cord blood primitive hematopoietic cells.

机构信息

Laboratory of Regeneromics, School of Pharmacy, Shanghai Jiao Tong University, Shanghai 200240, China.

出版信息

Biomed Pharmacother. 2010 Sep;64(7):482-6. doi: 10.1016/j.biopha.2010.01.005. Epub 2010 Mar 4.

Abstract

Wnt signaling pathway plays important roles in the biology of stem cells in maintaining their self-renewal property. Glycogen synthase kinase-3 (GSK-3) inhibitors, the Wnt signaling agonists, maintain the pluripotency of embryonic stem cells. We report here that a synthetic GSK-3 inhibitor, 6-bromoindirubin-3'-oxime (BIO), showed opposite effects on the expansion of human primitive hematopoietic cells isolated from umbilical cord blood (UCB). In combination with human c-kit ligand (KL), BIO at low concentration (0.2 μM) enhanced the expansion of UCB CD34+ cells, which was BIO structure and exposure time dependent; however, at high concentration (2 μM) it inhibited the expansion of the cells. Furthermore, hematopoietic stem cells (HSCs) were exhausted when the UCB CD34+ cells were exposed to 0.2 μM BIO and KL longer than 2 days. In conclusion, the use of BIO in expansion of UCB HSCs remains a significant challenge.

摘要

Wnt 信号通路在干细胞的生物学中起着重要作用,能维持其自我更新特性。糖原合成酶激酶-3(GSK-3)抑制剂是 Wnt 信号激动剂,能维持胚胎干细胞的多能性。我们在此报告,一种合成的 GSK-3 抑制剂 6-溴靛红-3'-肟(BIO)对从脐带血(UCB)中分离的人原始造血细胞的扩增表现出相反的效果。与人类 c-kit 配体(KL)联合使用时,低浓度(0.2 μM)的 BIO 增强了 UCB CD34+细胞的扩增,这与 BIO 的结构和暴露时间有关;然而,高浓度(2 μM)时则抑制了细胞的扩增。此外,当 UCB CD34+细胞暴露于 0.2 μM BIO 和 KL 超过 2 天时,造血干细胞(HSCs)被耗尽。总之,BIO 在 UCB HSCs 扩增中的应用仍然是一个重大挑战。

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