Grau Marijke, Kuck Lennart, Dietz Thomas, Bloch Wilhelm, Simmonds Michael J
Department of Molecular and Cellular Sports Medicine, German Sport University Cologne, 50933 Cologne, NRW, Germany.
Biorheology Research Laboratory, Menzies Health Institute Queensland, Griffith University, Gold Coast, QLD 4222, Australia.
Biology (Basel). 2021 Jan 11;10(1):47. doi: 10.3390/biology10010047.
Red blood cell (RBC) deformability is an essential component of microcirculatory function that appears to be enhanced by physiological shear stress, while being negatively affected by supraphysiological shears and/or free radical exposure. Given that blood contains RBCs with non-uniform physical properties, whether all cells equivalently tolerate mechanical and oxidative stresses remains poorly understood. We thus partitioned blood into old and young RBCs which were exposed to phenazine methosulfate (PMS) that generates intracellular superoxide and/or specific mechanical stress. Measured RBC deformability was lower in old compared to young RBCs. PMS increased total free radicals in both sub-populations, and RBC deformability decreased accordingly. Shear exposure did not affect reactive species in the sub-populations but reduced RBC nitric oxide synthase (NOS) activation and intriguingly increased RBC deformability in old RBCs. The co-application of PMS and shear exposure also improved cellular deformability in older cells previously exposed to reactive oxygen species (ROS), but not in younger cells. Outputs of NO generation appeared dependent on cell age; in general, stressors applied to younger RBCs tended to induce S-nitrosylation of RBC cytoskeletal proteins, while older RBCs tended to reflect markers of nitrosative stress. We thus present novel findings pertaining to the interplay of mechanical stress and redox metabolism in circulating RBC sub-populations.
红细胞(RBC)的可变形性是微循环功能的一个重要组成部分,生理剪切应力似乎能增强其可变形性,而超生理剪切力和/或自由基暴露则会对其产生负面影响。鉴于血液中含有物理性质不均匀的红细胞,目前对于所有细胞是否能同等耐受机械和氧化应激仍知之甚少。因此,我们将血液分为衰老红细胞和年轻红细胞,并使其暴露于能产生细胞内超氧化物和/或特定机械应力的硫酸吩嗪甲酯(PMS)中。结果发现,衰老红细胞的可变形性低于年轻红细胞。PMS增加了两个亚群中的总自由基含量,红细胞的可变形性也相应降低。剪切力暴露并未影响亚群中的活性物质,但降低了红细胞一氧化氮合酶(NOS)的活性,有趣的是,它增加了衰老红细胞的可变形性。同时施加PMS和剪切力暴露也改善了先前暴露于活性氧(ROS)的衰老细胞的细胞可变形性,但对年轻细胞没有效果。一氧化氮生成的输出似乎取决于细胞年龄;一般来说,施加于年轻红细胞的应激源往往会诱导红细胞细胞骨架蛋白的S-亚硝基化,而衰老红细胞则倾向于反映亚硝化应激的标志物。因此,我们提出了关于循环红细胞亚群中机械应力和氧化还原代谢相互作用的新发现。