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高渗环境下的冷诱导溶血

Cold-induced hemolysis in a hypertonic milieu.

作者信息

Green F A, Jung C Y

出版信息

J Membr Biol. 1977 May 12;33(3-4):249-62. doi: 10.1007/BF01869519.

Abstract

Suspension of human erythrocytes at 37 degrees C in an environment made hypertonic by increasing concentrations of sodium chloride and sucrose was followed by hemolysis when the temperature was lowered to 0 degrees C. Two distinct stages were involved in this hemolytic phenomenon, the first being incubation with hypertonic solute at some temperature above 20 degrees C with an increasing effect up to 45 degrees C, and the second stage consisting of lowering the temperature below 15 degrees C with increasing hemolysis down to 0 degrees C. The rate of cooling was not an important factor, but the presence of ions reduced the extent of cold-induced hemolysis in hypertonic sucrose. No significant release of membrane phospholipid and cholesterol accompanied this hemolysis. The solubilization of membrane protein components was investigated, with some differences appearing on sodium dodecyl sulfate polyacrylamide gel electrophoresis between hypertonic and isotonic supernatants. Spectrin could not be identified in solubilized form. Correlation of the temperatures of note in these studies with results from the literature on other biological effects of temperature-induced phase transitions in membrane lipids strongly points to the conclusion that such transitions are involved in the mechanism of cold-induced hypertonic hemolysis. It is postulated that the hypertonic milieu has resulted in membrane-protein alteration damage which prevents normal adaption to the new physical state of the membrane lipids during cooling.

摘要

将人红细胞悬浮于37℃、通过增加氯化钠和蔗糖浓度而使其变为高渗的环境中,当温度降至0℃时会发生溶血。这种溶血现象涉及两个不同阶段,第一个阶段是在高于20℃的某个温度下与高渗溶质孵育,直至45℃时作用增强;第二个阶段是将温度降至15℃以下,溶血程度随温度降至0℃而增加。冷却速率不是一个重要因素,但离子的存在会降低高渗蔗糖中冷诱导溶血的程度。这种溶血过程中没有伴随明显的膜磷脂和胆固醇释放。对膜蛋白成分的溶解情况进行了研究,在十二烷基硫酸钠聚丙烯酰胺凝胶电泳上,高渗上清液和等渗上清液之间出现了一些差异。在溶解形式中未鉴定出血影蛋白。这些研究中值得注意的温度与文献中关于温度诱导膜脂相变的其他生物学效应的结果之间的相关性,有力地表明这种相变参与了冷诱导高渗溶血的机制。据推测,高渗环境导致了膜蛋白改变损伤,从而在冷却过程中阻止了对膜脂新物理状态的正常适应。

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