Information Science and Engineering School, Lanzhou University, Lanzhou, 730000, China.
School of Biology, Lanzhou University, Lanzhou, 730000, China.
Chin J Integr Med. 2019 Dec;25(12):939-947. doi: 10.1007/s11655-018-3003-5. Epub 2018 Jun 25.
To explore the molecular-level mechanism on the hematopoiesis effect of Angelicae sinensis Radix (ASR) with systems-based interactome analysis.
This systems-based interactome analysis was designed to enforce the workflow of "ASR (herb)→compound→target protein→internal protein actions→ending regulated protein for hematopoiesis". This workflow was deployed with restrictions on regulated proteins expresses in bone marrow and anemia disease and futher validated with experiments.
The hematopoiesis mechanism of ASR might be accomplished through regulating pathways of cell proliferation towards hemopoiesis with cross-talking agents of spleen tyrosine kinase (SYK), Janus kinase 2 (JAK2), and interleukin-2-inducible T-cell kinase (ITK). The hematopoietic function of ASR was also validated by colony-forming assay performed on mice bone marrow cells. As a result, SYK, JAK2 and ITK were activated.
This study provides a new approach to systematically study and predict the therapeutic mechanism for ASR based on interactome analysis towards biological process with experimental validations.
通过系统互作分析探索当归补血作用的分子水平机制。
本系统互作分析旨在加强“当归(草药)→化合物→靶蛋白→内部蛋白作用→对造血有调节作用的终末蛋白”这一工作流程。该工作流程受到在骨髓和贫血疾病中表达的调节蛋白的限制,并通过实验进一步验证。
当归的造血机制可能是通过调节细胞增殖向造血的途径来完成的,其交叉作用剂为脾酪氨酸激酶(SYK)、Janus 激酶 2(JAK2)和白细胞介素 2 诱导的 T 细胞激酶(ITK)。当归的造血功能也通过对小鼠骨髓细胞进行集落形成实验得到了验证。结果表明,SYK、JAK2 和 ITK 被激活。
本研究通过实验验证,为基于互作分析对生物过程进行系统研究和预测当归治疗机制提供了一种新方法。