Adequate stimulation of hematopoietic stem cell proliferation by a polyherbal formulation (EMSA eritin) leading to lymphocyte differentiation in BALB/c mice after radiation

Mansur Ibrahim , Edi Widjajanto , M. Aris Widodo , Sutiman B. Sumitro
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引用次数: 3

Abstract

Radiotherapy is still an essential option for treatment of various stages of cancer. However, the irradiation administered would deplete the hematopoietic stem cells in the bone marrow, which would eventually decrease the number of lymphocytes and erythrocytes in the circulatory system. EMSA eritin is a polyherbal formulation that has the ability to stimulate erythropoiesis in mice after radiation therapy. Erythropoiesis is a complex mechanism involving the interaction of dozens of genes that may also be involved in other cellular process, such as lymphopoiesis. In this study, we elucidated the potential of EMSA eritin to stimulate other mechanisms, in addition to being an inducer of erythrocyte production. Bioinformatic analysis results indicated that the EMSA eritin formulation contains multiactive compounds that synergistically drive hematopoiesis and trigger lymphocyte differentiation. We then tested this prediction using an in vivo cell-culture system in a mice model. Experimental results suggested that EMSA eritin is able to induce hematopoietic stem cell proliferation and differentiate these cells into lymphocytes in BALB/c mice after sublethal radiation therapy. Moreover, the polyherbal formulation increased proliferation and survival of B and T lymphocytes in a dose-dependent manner. The results indicate that the polyherbal formulation is adequate to ameliorate both erythropoiesis and lymphopoiesis. The formulation thus appears very promising for treatment of patients following radiation therapy. However, this warrants further investigation.

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多羟基制剂(EMSA eritin)对BALB/c小鼠辐射后淋巴细胞分化的造血干细胞增殖的充分刺激
放射治疗仍然是治疗癌症不同阶段的重要选择。然而,照射会耗尽骨髓中的造血干细胞,最终会减少循环系统中淋巴细胞和红细胞的数量。EMSA eritin是一种多羟基制剂,能够刺激放射治疗后小鼠的红细胞生成。红细胞生成是一种复杂的机制,涉及数十个基因的相互作用,这些基因也可能参与其他细胞过程,如淋巴细胞生成。在本研究中,我们阐明了EMSA eritin除了作为红细胞产生的诱导剂外,还具有刺激其他机制的潜力。生物信息学分析结果表明,EMSA eritin制剂含有协同驱动造血和触发淋巴细胞分化的多种活性化合物。然后,我们在小鼠模型中使用体内细胞培养系统测试了这一预测。实验结果表明,EMSA-eritin能诱导BALB/c小鼠亚致死性放疗后的造血干细胞增殖并分化为淋巴细胞。此外,多羟基制剂以剂量依赖的方式增加了B和T淋巴细胞的增殖和存活。结果表明,多羟基制剂足以改善红细胞生成和淋巴生成。因此,该制剂对于放射治疗后的患者的治疗似乎非常有希望。然而,这需要进一步调查。
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