Salerno Luca, Cosentino Carlo, Morrone Giovanni, Amato Francesco
Laboratory of Biomechatronics, Department of Experimental and Clinical Medicine, University Magna Græcia of Catanzaro, Catanzaro, Italy.
Laboratory of Molecular Haematopoiesis and Stem Cell Biology, Department of Experimental and Clinical Medicine, University Magna Græcia of Catanzaro, Catanzaro, Italy.
PLoS One. 2015 Jul 13;10(7):e0132208. doi: 10.1371/journal.pone.0132208. eCollection 2015.
Despite progresses in identifying the cellular mechanisms at the basis of the differentiation of hematopoietic stem/progenitor cells, little is known about the regulatory circuitry at the basis of lineage commitment of hematopoietic multipotent progenitors. To address this issue, we propose a computational approach to give further insights in the comprehension of this genetic mechanism. Differently from T lymphopoiesis, however, there is at present no mathematical model describing lineage restriction of multipotent progenitors to early B-cell precursors. Here, we provide a first model-constructed on the basis of current experimental evidence from literature and of publicly available microarray datasets-of the genetic regulatory network driving the cellular fate determination at the stage of lymphoid lineage commitment, with particular regard to the multipotent-B-cell progenitor transition. By applying multistability analysis methods, we are able to assess the capability of the model to capture the experimentally observed switch-like commitment behavior. These methods allow us to confirm the central role of zinc finger protein 521 (ZNF521) in this process, that we had previously reported, and to identify a novel putative functional interaction for ZNF521, which is essential to realize such characteristic behavior. Moreover, using the devised model, we are able to rigorously analyze the mechanisms underpinning irreversibility of the physiological commitment step and to devise a possible reprogramming strategy, based on the combined modification of the expression of ZNF521 and EBF1.
尽管在确定造血干/祖细胞分化的细胞机制方面取得了进展,但对于造血多能祖细胞谱系定向的调控网络却知之甚少。为了解决这个问题,我们提出了一种计算方法,以便在理解这种遗传机制方面提供进一步的见解。然而,与T淋巴细胞生成不同的是,目前尚无数学模型描述多能祖细胞向早期B细胞前体的谱系限制。在此,我们基于文献中的当前实验证据和公开可用的微阵列数据集,提供了第一个驱动淋巴细胞谱系定向阶段细胞命运决定的遗传调控网络模型,特别是关于多能B细胞祖细胞的转变。通过应用多稳定性分析方法,我们能够评估该模型捕捉实验观察到的开关样定向行为的能力。这些方法使我们能够证实锌指蛋白521(ZNF521)在这一过程中的核心作用,这是我们之前报道过的,并确定了ZNF521一种新的假定功能相互作用,这对于实现这种特征行为至关重要。此外,使用所设计的模型,我们能够严格分析生理定向步骤不可逆性的潜在机制,并基于对ZNF521和EBF1表达的联合修饰设计一种可能的重编程策略。