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红细胞储存会诱导红细胞自杀性死亡。

Storage of Erythrocytes Induces Suicidal Erythrocyte Death.

作者信息

Lang Elisabeth, Pozdeev Vitaly I, Xu Haifeng C, Shinde Prashant V, Behnke Kristina, Hamdam Junnat M, Lehnert Erik, Scharf Rüdiger E, Lang Florian, Häussinger Dieter, Lang Karl S, Lang Philipp A

机构信息

Department of Gastroenterology, Hepatology and Infectiology, University of Dx00FC;sseldorf, Dx00FC;sseldorf, Germany.

出版信息

Cell Physiol Biochem. 2016;39(2):668-76. doi: 10.1159/000445657. Epub 2016 Jul 21.

Abstract

BACKGROUND/AIMS: Similar to apoptosis of nucleated cells, red blood cells (RBC) can undergo suicidal cell death - called eryptosis. It is characterized by cell shrinkage and phosphatidylserine translocation. Eryptosis is triggered by an increase of intracellular calcium concentration due to activation of nonselective cation channels. The cation channels and consequently eryptosis are inhibited by erythropoietin. Eryptotic RBC are engulfed by macrophages and thus rapidly cleared from circulating blood. In this study, we explored whether storage of RBC influences the rate of eryptosis.

METHODS

Flow cytometry was employed to quantify phosphatidylserine exposing erythrocytes from annexin V binding and cytosolic Ca2+ activity from Fluo-3 fluorescence. Clearance of stored murine RBC was tested by injection of carboxyfluorescein succinimidyl ester (CFSE)-labelled erythrocytes.

RESULTS

Storage for 42 days significantly increased the percentage of phosphatidylserine exposing and haemolytic erythrocytes, an effect blunted by removal of extracellular calcium. Phosphatidylserine exposure could be inhibited by addition of erythropoietin. Upon transfusion, the clearance of murine CFSE-labelled RBC from circulating blood was significantly higher following storage for 10 days when compared to 2 days of storage.

CONCLUSION

Storage of RBC triggers eryptosis by Ca2+ and erythropoietin sensitive mechanisms.

摘要

背景/目的:与有核细胞的凋亡类似,红细胞(RBC)可经历自杀性细胞死亡——称为红细胞凋亡。其特征为细胞皱缩和磷脂酰丝氨酸易位。红细胞凋亡由非选择性阳离子通道激活导致细胞内钙浓度升高所触发。阳离子通道以及由此引发的红细胞凋亡受促红细胞生成素抑制。发生凋亡的红细胞被巨噬细胞吞噬,从而迅速从循环血液中清除。在本研究中,我们探究了红细胞储存是否会影响红细胞凋亡率。

方法

采用流式细胞术通过膜联蛋白V结合来定量磷脂酰丝氨酸暴露的红细胞,并通过Fluo - 3荧光来测定胞质Ca2+活性。通过注射羧基荧光素琥珀酰亚胺酯(CFSE)标记的红细胞来检测储存的小鼠红细胞的清除情况。

结果

储存42天显著增加了磷脂酰丝氨酸暴露的红细胞和溶血红细胞的百分比,去除细胞外钙可减弱这一效应。添加促红细胞生成素可抑制磷脂酰丝氨酸暴露。输血时,与储存2天相比,储存10天后小鼠CFSE标记的红细胞从循环血液中的清除率显著更高。

结论

红细胞储存通过钙和促红细胞生成素敏感机制触发红细胞凋亡。

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