Thiagarajan Perumal, Parker Charles J, Prchal Josef T
Center for Translational Research on Inflammatory Diseases (CTRID), Michael E. DeBakey Veterans Affairs Medical Center, Houston, TX, United States.
Department of Pathology and Immunology, Baylor College of Medicine, Houston, TX, United States.
Front Physiol. 2021 Mar 15;12:655393. doi: 10.3389/fphys.2021.655393. eCollection 2021.
Normal human red blood cells have an average life span of about 120 days in the circulation after which they are engulfed by macrophages. This is an extremely efficient process as macrophages phagocytose about 5 million erythrocytes every second without any significant release of hemoglobin in the circulation. Despite large number of investigations, the precise molecular mechanism by which macrophages recognize senescent red blood cells for clearance remains elusive. Red cells undergo several physicochemical changes as they age in the circulation. Several of these changes have been proposed as a recognition tag for macrophages. Most prevalent hypotheses for red cell clearance mechanism(s) are expression of neoantigens on red cell surface, exposure phosphatidylserine and decreased deformability. While there is some correlation between these changes with aging their causal role for red cell clearance has not been established. Despite plethora of investigations, we still have incomplete understanding of the molecular details of red cell clearance. In this review, we have reviewed the recent data on clearance of senescent red cells. We anticipate recent progresses in red cell labeling and the explosion of modern proteomic techniques will, in near future, facilitate our understanding of red cell senescence and their destruction.
正常人类红细胞在循环系统中的平均寿命约为120天,之后它们会被巨噬细胞吞噬。这是一个极其高效的过程,因为巨噬细胞每秒吞噬约500万个红细胞,而不会在循环系统中大量释放血红蛋白。尽管进行了大量研究,但巨噬细胞识别衰老红细胞以进行清除的确切分子机制仍然难以捉摸。红细胞在循环中衰老时会发生多种物理化学变化。其中一些变化已被提出作为巨噬细胞的识别标记。关于红细胞清除机制最普遍的假说是红细胞表面新抗原的表达、磷脂酰丝氨酸的暴露和变形性降低。虽然这些变化与衰老之间存在一定的相关性,但它们在红细胞清除中的因果作用尚未确定。尽管进行了大量研究,我们对红细胞清除的分子细节仍未完全了解。在这篇综述中,我们回顾了有关衰老红细胞清除的最新数据。我们预计,红细胞标记技术的最新进展以及现代蛋白质组学技术的蓬勃发展将在不久的将来促进我们对红细胞衰老及其破坏的理解。