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JAK2/STAT5 信号通路介导了补骨脂当归汤增强造血功能。

JAK2/STAT5 signaling pathway mediates Bojungbangdocktang enhanced hematopoiesis.

机构信息

College of Oriental Medicine, Kyung Hee University, Dongdaemun-gu, Seoul, Republic of Korea.

出版信息

Phytother Res. 2011 Mar;25(3):329-37. doi: 10.1002/ptr.3257.

DOI:10.1002/ptr.3257
PMID:20669261
Abstract

Bojungbangdocktang (BJBDT) is a medicinal herbal cocktail that has been used for cancer prevention and treatment in traditional Korean medicine. In the current study, BJBDT was demonstrated to regulate hematopoiesis. BJBDT significantly increased the expression of hematopoietic cytokines interleukin (IL)-3, stem cell factor (SCF), granulocyte-macrophage-colony stimulating factor (GM-CSF), thrombopoietin (TPO) and erythropoietin (EPO) at the level of mRNA and secretion in hematopoietic stem cells (HSCs). Additionally, BJBDT enhanced the phosphorylation of Janus activated kinase 2 (JAK2) and signal transducer and activator of transcription 5 (STAT5) and STAT binding to gamma interferon activated sites (GAS) in HSCs. Furthermore, BJBDT significantly enhanced the growth rate of granulocyte erythrocyte monocyte macrophage colony-forming units (CFU-GEMM) and erythroid burst forming units (BFU-E) in vitro. Moreover, BJBDT increased the level of EPO at mRNA in kidney and plasma, and the numbers of erythroid-specific antigen Ter-119(+) erythroid cells in mice with aplastic anemia induced by 20% benzene. Consistently, histochemical staining revealed BJBDT increased the bone marrow and stromal cells as well as decreased macrophages and adipocytes in bone marrow tissues of mice with aplastic anemia. Taken together, the results suggest that BJBDT can enhance hematopoiesis via hematopoietic cytokine-mediated JAK2/STAT5 pathway as a potent hematopoietic candidate. Copyright © 2010 John Wiley & Sons, Ltd.

摘要

Bojungbangdocktang (BJBDT) 是一种草药鸡尾酒,在传统的韩国医学中被用于癌症的预防和治疗。在目前的研究中,BJBDT 被证明可以调节造血。BJBDT 显著增加了造血细胞因子白细胞介素 (IL)-3、干细胞因子 (SCF)、粒细胞-巨噬细胞集落刺激因子 (GM-CSF)、血小板生成素 (TPO) 和促红细胞生成素 (EPO) 在 mRNA 水平和造血干细胞 (HSCs) 中的分泌。此外,BJBDT 增强了 HSCs 中 Janus 激活激酶 2 (JAK2) 和信号转导和转录激活因子 5 (STAT5) 的磷酸化以及 STAT 与 γ干扰素激活位点 (GAS) 的结合。此外,BJBDT 显著增强了体外粒细胞红细胞单核细胞巨噬细胞集落形成单位 (CFU-GEMM) 和红系爆式集落形成单位 (BFU-E) 的生长速度。此外,BJBDT 增加了再生障碍性贫血小鼠肾和血浆中 EPO 的 mRNA 水平,以及苯诱导的 20%再生障碍性贫血小鼠中红系特异性抗原 Ter-119(+)红细胞的数量。一致地,组织化学染色显示 BJBDT 增加了骨髓和基质细胞,减少了骨髓组织中的巨噬细胞和脂肪细胞。综上所述,这些结果表明,BJBDT 可以通过造血细胞因子介导的 JAK2/STAT5 途径增强造血,作为一种有效的造血候选物。版权所有 © 2010 约翰威立父子公司

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