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血红素诱导的自杀性红细胞死亡。

Hemin-induced suicidal erythrocyte death.

作者信息

Gatidis Sergios, Föller Michael, Lang Florian

机构信息

Department of Physiology, University of Tübingen, Tübingen, Germany.

出版信息

Ann Hematol. 2009 Aug;88(8):721-6. doi: 10.1007/s00277-009-0697-7. Epub 2009 Jan 29.

Abstract

Several diseases, such as malaria, sickle cell disease, and ischemia/reperfusion may cause excessive formation of hemin, which may in turn trigger hemolysis. A variety of drugs and diseases leading to hemolysis triggers suicidal erythrocyte death or eryptosis, i.e., cell membrane scrambling and cell shrinkage. Eryptosis is elicited by increased cytosolic Ca(2+) activity and by ceramide. The present study explored whether hemin stimulates eryptosis. Cell membrane scrambling was estimated from annexin V-binding to phosphatidylserine exposed at the cell surface, cell shrinkage from forward scatter in fluorescence-activated cell sorter analysis, cytosolic Ca(2+) activity from Fluo3 fluorescence and ceramide formation from fluorescence-labeled antibody binding. Exposure to hemin (1-10 microM) within 48 h significantly increased annexin V-binding, decreased forward scatter, increased cytosolic Ca(2+) activity, and stimulated ceramide formation. In conclusion, hemin stimulates suicidal cell death, which may in turn contribute to the clearance of circulating erythrocytes and thus to anemia.

摘要

几种疾病,如疟疾、镰状细胞病和缺血/再灌注,可能导致血红素过度生成,进而引发溶血。多种导致溶血的药物和疾病会引发自杀性红细胞死亡或红细胞凋亡,即细胞膜紊乱和细胞收缩。红细胞凋亡由胞质Ca(2+)活性增加和神经酰胺引发。本研究探讨了血红素是否刺激红细胞凋亡。通过膜联蛋白V与细胞表面暴露的磷脂酰丝氨酸结合来评估细胞膜紊乱,通过荧光激活细胞分选分析中的前向散射来评估细胞收缩,通过Fluo3荧光评估胞质Ca(2+)活性,通过荧光标记抗体结合评估神经酰胺形成。在48小时内暴露于血红素(1 - 10微摩尔)显著增加了膜联蛋白V结合、降低了前向散射、增加了胞质Ca(2+)活性并刺激了神经酰胺形成。总之,血红素刺激自杀性细胞死亡,这反过来可能有助于清除循环中的红细胞,从而导致贫血。

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