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草药鸡尾酒 ka-mi-kae-kyuk-tang 可刺激小鼠骨髓造血干细胞和 Janus 激活激酶 2/信号转导子和转录激活因子 5 通路。

Herbal cocktail ka-mi-kae-kyuk-tang stimulates mouse bone marrow stem cell hematopoiesis and janus-activated kinase 2/signal transducer and activator of transcription 5 pathway.

机构信息

College of Oriental Medicine, Kyung Hee University, Seoul, South Korea.

出版信息

Am J Chin Med. 2011;39(6):1235-52. doi: 10.1142/S0192415X11009524.

Abstract

Ka-mi-kae-kyuk-tang (KMKKT) is an Oriental herbal medicinal cocktail. Our collaborative team has shown that it has potent anti-angiogenic, anti-cancer and anti-metastatic activities in vivo without observable side effects. We have documented evidence for KMKKT to alleviate drug-induced hematotoxicity in vivo. In the present study, we investigated the mechanistic and signaling events through which KMKKT enhances hematopoiesis, using hematopoietic stem cells (HSCs) isolated from the bone marrow of 8-12 week-old C57BL/6 mice. Our results show that KMKKT significantly increased the expression of the 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 HSCs. KMKKT also increased the expression of c-Kit, a cytokine receptor expressed in HSCs. In addition, KMKKT enhanced phosphorylation of Janus kinase 2 (JAK2) and signal transducer and activator of transcription 5 (STAT5), and increased the binding activity of STAT5 to gamma interferon activated sites (GAS) that mediate JAK2 downstream signaling. Furthermore, we found that KMKKT significantly enhanced the growth rate of colony-forming unit granulocyte erythrocyte monocyte macrophages (CFU-GEMM) and burst forming unit erythroid (BFU-E) of mouse HSCs (mHSCs) stimulated by IL-3/EPO. Overall, our results demonstrated that KMKKT alleviated drug-induced side effects through enhanced hematopoiesis, at least in part through cytokine-mediated JAK2/STAT5 signaling.

摘要

加味开金锁汤是一种东方草药鸡尾酒。我们的合作团队已经证明,它在体内具有强大的抗血管生成、抗癌和抗转移活性,没有观察到明显的副作用。我们有文件证据表明,加味开金锁汤可以减轻体内药物引起的血液毒性。在本研究中,我们使用从 8-12 周龄 C57BL/6 小鼠骨髓中分离的造血干细胞 (HSCs) 研究了加味开金锁汤增强造血作用的机制和信号事件。我们的结果表明,加味开金锁汤显著增加了 HSCs 中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) 的表达,mRNA 和分泌水平。加味开金锁汤还增加了 HSCs 中表达的细胞因子受体 c-Kit 的表达。此外,加味开金锁汤增强了 Janus 激酶 2 (JAK2) 和信号转导和转录激活因子 5 (STAT5) 的磷酸化,并增加了 STAT5 与介导 JAK2 下游信号的 γ干扰素激活位点 (GAS) 的结合活性。此外,我们发现加味开金锁汤显著增强了由白细胞介素 3/促红细胞生成素 (IL-3/EPO) 刺激的小鼠 HSCs (mHSCs) 的集落形成单位粒细胞红细胞单核巨噬细胞 (CFU-GEMM) 和爆式形成单位红细胞 (BFU-E) 的生长速度。总的来说,我们的结果表明,加味开金锁汤通过增强造血作用缓解了药物引起的副作用,至少部分是通过细胞因子介导的 JAK2/STAT5 信号通路。

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