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大鼠和人类红细胞对外源Ca2+的不同敏感性。

Different sensitivities of rat and human red cells to exogenous Ca2+.

作者信息

Swislocki N I, Tierney J M

机构信息

Department of Biochemistry, UMDNJ-New Jersey Medical School, Newark 07103-2757.

出版信息

Am J Hematol. 1989 May;31(1):1-10. doi: 10.1002/ajh.2830310102.

Abstract

During an examination of the effects of shear and of the Ca2+ ionophore A23187 on Ca2+ entry into erythrocytes of rats and humans, we noted that rat erythrocytes were much more sensitive to Ca2+-induced hemolysis than the human cells. An examination of the effect of Ca2+ on transglutaminase, a cytosolic enzyme in the erythrocyte which cross-links membrane proteins and renders cells less deformable, demonstrated a correlation between enzyme activity and Ca2+-induced hemolysis. Both rat and human cells subjected to shear-induced Ca2+ entry exhibited increased enzyme activity and altered membrane protein SDS-PAGE patterns. Twenty micromolar A23187 with Ca2+ at concentrations above 80 microM caused hemolysis of rat erythrocytes. In contrast to human erythrocytes, under these conditions no membranes were recoverable from rat erythrocytes. At lower concentrations of Ca2+ (25 and 50 microM), however, rat erythrocytes maintained integrity, and exhibited enhanced transglutaminase activity and cross-linking of membrane proteins. The rat enzyme can be activated 30% by 10 microM Ca2+, while 50 microM Ca2+ was necessary to achieve a similar activation of the enzyme from human red blood cells. In studies of shear-stimulated Ca2+ uptake by erythrocytes the rat red cell enzyme was more readily activated. The SDS-PAGE pattern of rat red cell membranes after a 30 sec shear showed specific changes in protein banding, including the appearance of bands greater than 330 kDa. Changes in protein banding were also apparent in cytosolic proteins. This work supports the view that shear-induced Ca2+ entry activates transglutaminase that leads to cross-linking of membrane components, a loss of cell integrity, and eventual cell death.

摘要

在研究剪切力和钙离子载体A23187对大鼠和人类红细胞钙离子内流的影响时,我们注意到大鼠红细胞对钙离子诱导的溶血比人类细胞敏感得多。研究钙离子对转谷氨酰胺酶(一种红细胞胞质酶,可使膜蛋白交联并使细胞变形性降低)的影响发现,酶活性与钙离子诱导的溶血之间存在相关性。受到剪切力诱导钙离子内流作用的大鼠和人类细胞均表现出酶活性增加以及膜蛋白SDS-PAGE图谱改变。20微摩尔的A23187与浓度高于80微摩尔的钙离子共同作用会导致大鼠红细胞溶血。与人类红细胞不同,在这些条件下,大鼠红细胞无法回收细胞膜。然而,在较低的钙离子浓度(25和50微摩尔)下,大鼠红细胞保持完整,并表现出转谷氨酰胺酶活性增强和膜蛋白交联。大鼠的这种酶可被10微摩尔钙离子激活30%,而人类红细胞中的酶则需要50微摩尔钙离子才能实现类似程度的激活。在红细胞剪切力刺激钙离子摄取的研究中,大鼠红细胞的酶更容易被激活。30秒剪切力作用后大鼠红细胞膜的SDS-PAGE图谱显示蛋白条带出现特定变化,包括出现大于330 kDa的条带。胞质蛋白的条带也有明显变化。这项工作支持以下观点:剪切力诱导的钙离子内流激活转谷氨酰胺酶,导致膜成分交联、细胞完整性丧失并最终导致细胞死亡。

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