Bernhardt Ingolf, Nguyen Duc Bach, Wesseling Mauro C, Kaestner Lars
Laboratory of Biophysics, Faculty of Natural Science and Technology, Saarland University, Saarbrücken, Germany.
Experimental Physics, Faculty of Natural Science and Technology, Saarland University, Saarbrücken, Germany.
Front Physiol. 2020 Jan 10;10:1629. doi: 10.3389/fphys.2019.01629. eCollection 2019.
After about 120 days of circulation in the blood stream, erythrocytes are cleared by macrophages in the spleen and the liver. The "eat me" signal of this event is thought to be the translocation of phosphatidylserine from the inner to the outer membrane leaflet due to activation of the scramblase, while the flippase is inactivated. Both processes are triggered by an increased intracellular Ca concentration. Although this is not the only mechanism involved in erythrocyte clearance, in this minireview, we focus on the following questions: Is the intracellular-free Ca concentration and hence phosphatidylserine exposure dependent on the erythrocyte age, i.e. is the Ca concentration, progressively raising during the erythrocyte aging ? Can putative differences in intracellular Ca and exposure of phosphatidylserine to the outer membrane leaflet be measured in age separated cell populations? Literature research revealed less than dozen of such publications with vastly contradicting results for the Ca concentrations but consistency for a lack of change for the phosphatidylserine exposure. Additionally, we performed reanalysis of published data resulting in an ostensive illustration of the situation described above. Relating these results to erythrocyte physiology and biochemistry, we can conclude that the variation of the intracellular free Ca concentration is limited with 10 μM as the upper level of the concentration. Furthermore, we propose the hypothesis that variations in measured Ca concentrations may to a large extent depend on the experimental conditions applied but reflect a putatively changed Ca susceptibility of erythrocytes in dependence of cell age.
在血流中循环约120天后,红细胞被脾脏和肝脏中的巨噬细胞清除。这一过程的“自我吞噬”信号被认为是由于磷脂酰丝氨酸翻转酶激活,同时磷脂酰丝氨酸转位酶失活,导致磷脂酰丝氨酸从内膜小叶转移到外膜小叶。这两个过程均由细胞内钙离子浓度升高触发。尽管这不是红细胞清除过程中唯一涉及的机制,但在本综述中,我们关注以下问题:细胞内游离钙离子浓度以及因此导致的磷脂酰丝氨酸暴露是否取决于红细胞的年龄,即钙离子浓度是否在红细胞衰老过程中逐渐升高?能否在按年龄分离的细胞群体中检测到细胞内钙离子和磷脂酰丝氨酸在外膜小叶暴露的假定差异?文献研究表明,此类出版物不足十几篇,关于钙离子浓度的结果差异很大,但磷脂酰丝氨酸暴露缺乏变化这一点是一致的。此外,我们对已发表的数据进行了重新分析,从而直观地展示了上述情况。将这些结果与红细胞生理学和生物化学联系起来,我们可以得出结论,细胞内游离钙离子浓度的变化有限,浓度上限为10μM。此外,我们提出一个假设,即所测钙离子浓度的变化在很大程度上可能取决于所采用的实验条件,但反映了红细胞对钙离子敏感性可能随细胞年龄而发生的变化。