Arias Clemente Fernandez, Arias Cristina Fernandez
Departamento de Matemática Aplicada, Universidad Complutense de Madrid, Spain.
Grupo Interdisciplinar de Sistemas Complejos, Madrid, Spain.
R Soc Open Sci. 2017 Apr 5;4(4):160850. doi: 10.1098/rsos.160850. eCollection 2017 Apr.
Human red blood cells (RBCs) are normally phagocytized by macrophages of splenic and hepatic sinusoids at 120 days of age. The destruction of RBCs is ultimately controlled by antagonist effects of phosphatidylserine (PS) and CD47 on the phagocytic activity of macrophages. In this work, we introduce a conceptual model that explains RBC lifespan as a consequence of the dynamics of these molecules. Specifically, we suggest that PS and CD47 define a molecular algorithm that sets the timing of RBC phagocytosis. We show that significant changes in RBC lifespan described in the literature can be explained as alternative outcomes of this algorithm when it is executed in different conditions of oxygen availability. The theoretical model introduced here provides a unified framework to understand a variety of empirical observations regarding RBC biology. It also highlights the role of RBC lifespan as a key element of RBC homeostasis.
人类红细胞(RBCs)通常在120日龄时被脾脏和肝血窦的巨噬细胞吞噬。红细胞的破坏最终由磷脂酰丝氨酸(PS)和CD47对巨噬细胞吞噬活性的拮抗作用控制。在这项工作中,我们引入了一个概念模型,该模型将红细胞寿命解释为这些分子动态变化的结果。具体而言,我们认为PS和CD47定义了一种分子算法,该算法设定了红细胞吞噬的时间。我们表明,文献中描述的红细胞寿命的显著变化可以解释为该算法在不同氧可用性条件下执行时的不同结果。这里介绍的理论模型提供了一个统一的框架,以理解关于红细胞生物学的各种实证观察结果。它还强调了红细胞寿命作为红细胞内环境稳定关键要素的作用。