Wildenauer D B, Reuther H, Remien J
Biochim Biophys Acta. 1980 Dec 2;603(1):101-16. doi: 10.1016/0005-2736(80)90394-6.
The influence of tris(2-chloroethyl)amine on shape changes of human erythrocytes and ghosts was studied in vitro and correlated with alterations in the molecular structure of the membrane. (1) Reaction with 1--2 mM tris(2-chloroethyl)amine, a concentration which caused polymerisation of spectrin as detected by sodium dodecyl sulphate polyacrylamide gel electrophoresis, protected intact erythrocytes against metabolically induced shape changes. (2) When induced by Mg2+-ATP, ghosts porepared from alkylated erythrocytes underwent normal changes in shape. However, when ghosts were treated directly with tris(2-chloroethyl)amine, no Mg2+-ATP-induced shape changes occurred. This fixation in shape appeared to be due to a higher degree of reaction with the alkylating agent. (3) The amount of chlorpromazine necessary for transformation of erythrocytes into stomatocytes was increased for tris(2-chloroethyl)amine-pretreated cells and was dependent on the degree of reaction with tris(2-chloroethyl)amine. (4) Deformability of red cells after reaction with tris(2-chloroethyl)amine was estimated by measuring their rheological behaviour in glass capillary arrays. A slight reduction of the flow rate was observed for cells alkylated with 1--2 mM tris(2-chloroethyl)amine. (5) Extractability of spectrin was diminished and corresponded to the degree of spectrin polymerisation. (6) No difference in the incorporation of 32P by alkylated and untreated cells was found. Sodium dodecyl sulphate polyacrylamide gel electrophoresis and autoradiography of the membrane proteins from 32-P-treated cells showed that the spectrin component 2 and the polymerisation products generated by the reaction with tris(2-chloroethyl)amine were labelled. It is suggested that the observed conservation of cell shape is preferentially caused by the reaction of tris(2-chloroethyl)amine with spectrin.
在体外研究了三(2-氯乙基)胺对人红细胞和血影形状变化的影响,并将其与膜分子结构的改变相关联。(1)与1-2 mM三(2-氯乙基)胺反应,该浓度通过十二烷基硫酸钠聚丙烯酰胺凝胶电泳检测可导致血影蛋白聚合,能保护完整红细胞免受代谢诱导的形状变化。(2)当由Mg2+-ATP诱导时,由烷基化红细胞制备的血影会发生正常的形状变化。然而,当血影直接用三(2-氯乙基)胺处理时,Mg2+-ATP诱导的形状变化未发生。这种形状固定似乎是由于与烷基化剂的反应程度更高。(3)将红细胞转化为口形细胞所需的氯丙嗪量对于经三(2-氯乙基)胺预处理的细胞增加,并且取决于与三(2-氯乙基)胺的反应程度。(4)通过测量红细胞在玻璃毛细管阵列中的流变行为来估计与三(2-氯乙基)胺反应后红细胞的变形能力。用1-2 mM三(2-氯乙基)胺烷基化的细胞观察到流速略有降低。(5)血影蛋白的可提取性降低,并且与血影蛋白聚合程度相对应。(6)未发现烷基化细胞和未处理细胞在32P掺入方面存在差异。对来自32P处理细胞的膜蛋白进行十二烷基硫酸钠聚丙烯酰胺凝胶电泳和放射自显影显示,血影蛋白组分2和与三(2-氯乙基)胺反应产生的聚合产物被标记。有人提出,观察到的细胞形状保留优先是由三(2-氯乙基)胺与血影蛋白的反应引起的。