Danielczok Jens G, Terriac Emmanuel, Hertz Laura, Petkova-Kirova Polina, Lautenschläger Franziska, Laschke Matthias W, Kaestner Lars
Institute for Molecular Cell Biology, Saarland University, Homburg, Germany.
Experimental Physics, Saarland University, Saarbrücken, Germany.
Front Physiol. 2017 Dec 5;8:979. doi: 10.3389/fphys.2017.00979. eCollection 2017.
When red blood cells (RBCs) pass constrictions or small capillaries they need to pass apertures falling well below their own cross section size. We used different means of mechanical stimulations (hypoosmotic swelling, local mechanical stimulation, passing through microfluidic constrictions) to observe cellular responses of human RBCs in terms of intracellular Ca-signaling by confocal microscopy of Fluo-4 loaded RBCs. We were able to confirm our results in a mouse dorsal skinfold chamber model showing a transiently increased intracellular Ca when RBCs were passing through small capillaries . Furthermore, we performed the above-mentioned experiments as well as measurements of RBCs filterability under various pharmacological manipulations (GsMTx-4, TRAM-34) to explore the molecular mechanism of the Ca-signaling. Based on these experiments we conclude that mechanical stimulation of RBCs activates mechano-sensitive channels most likely Piezo1. This channel activity allows Ca to enter the cell, leading to a transient activation of the Gardos-channel associated with K, Cl, and water loss, i.e., with a transient volume adaptation facilitating the passage of the RBCs through the constriction.
当红细胞(RBCs)通过狭窄处或小毛细血管时,它们需要通过远小于自身横截面大小的孔径。我们使用了不同的机械刺激方法(低渗肿胀、局部机械刺激、通过微流体狭窄处),通过对加载了Fluo-4的红细胞进行共聚焦显微镜观察,来观察人类红细胞在细胞内钙信号方面的细胞反应。我们能够在小鼠背部皮褶腔室模型中证实我们的结果,该模型显示当红细胞通过小毛细血管时细胞内钙会短暂增加。此外,我们进行了上述实验以及在各种药理学操作(GsMTx-4、TRAM-34)下对红细胞过滤性的测量,以探索钙信号的分子机制。基于这些实验,我们得出结论,对红细胞的机械刺激会激活机械敏感通道,最有可能是Piezo1。这种通道活性允许钙进入细胞,导致与钾、氯和水分流失相关的Gardos通道短暂激活,即通过短暂的体积适应促进红细胞通过狭窄处。