Ikonomi Nensi, Kühlwein Silke D, Schwab Julian D, Kestler Hans A
Institute of Medical Systems Biology, Ulm University, Ulm, Germany.
Front Physiol. 2020 Jul 31;11:848. doi: 10.3389/fphys.2020.00848. eCollection 2020.
Hematopoietic stem cells (HSCs) provide all types of blood cells during the entire life of the organism. HSCs are mainly quiescent and can eventually enter the cell cycle to differentiate. HSCs are maintained and tightly regulated in a particular environment. The stem cell niche regulates dormancy and awakening. Deregulations of this interplay can lead to hematopoietic failure and diseases. In this paper, we present a Boolean network model that recapitulates HSC regulation in virtue of external signals coming from the niche. This Boolean network integrates and summarizes the current knowledge of HSC regulation and is based on extensive literature research. Furthermore, dynamic simulations suggest a novel systemic regulation of TP53 in homeostasis. Thereby, our model indicates that TP53 activity is balanced depending on external stimulations, engaging a regulatory mechanism involving ROS regulators and RAS activated transcription factors. Finally, we investigated different mouse models and compared them to knockout simulations. Here, the model could recapitulate observed behaviors and thus sustains our results.
造血干细胞(HSCs)在生物体的整个生命周期中产生所有类型的血细胞。造血干细胞主要处于静止状态,最终可进入细胞周期进行分化。造血干细胞在特定环境中得以维持并受到严格调控。干细胞微环境调节休眠和唤醒。这种相互作用的失调可导致造血功能衰竭和疾病。在本文中,我们提出了一个布尔网络模型,该模型借助来自微环境的外部信号概括了造血干细胞的调控。这个布尔网络整合并总结了造血干细胞调控的当前知识,并且基于广泛的文献研究。此外,动态模拟表明TP53在稳态中存在一种新的系统调控。因此,我们的模型表明,TP53的活性根据外部刺激而平衡,涉及一种包括ROS调节因子和RAS激活转录因子的调控机制。最后,我们研究了不同的小鼠模型,并将它们与基因敲除模拟进行比较。在此,该模型能够概括观察到的行为,从而支持了我们的结果。