首页> 外文OA文献 >TRANSIENT HOLES IN THE ERYTHROCYTE MEMBRANE DURING HYPOTONIC HEMOLYSIS AND STABLE HOLES IN THE MEMBRANE AFTER LYSIS BY SAPONIN AND LYSOLECITHIN
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TRANSIENT HOLES IN THE ERYTHROCYTE MEMBRANE DURING HYPOTONIC HEMOLYSIS AND STABLE HOLES IN THE MEMBRANE AFTER LYSIS BY SAPONIN AND LYSOLECITHIN

机译:低渗性溶血过程中红细胞膜的瞬态孔和皂角苷和溶血鞘磷脂溶解后膜中的稳定孔

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摘要

Ferritin and colloidal gold were found to permeate human erythrocytes during rapid or gradual hypotonic hemolysis. Only hemolysed cells contained these particles; adjacent intact cells did not contain the tracers. Ferritin or gold added 3 min after the onset of hypotonic hemolysis did not permeate the ghost cells which had, therefore, become transiently permeable. By adding ferritin at various times after the onset of hemolysis, it was determined that for the majority of the cells the permeable state (or interval between the time of development and closure of membrane holes) existed only from about 15 to 25 sec after the onset of hemolysis. It was possible to fix the transient "holes" in the open position by adding glutaraldehyde only between 10 and 20 sec after the onset of hemolysis. The existence of such fixed holes was shown by the cell entry of ferritin and gold which were added to these prefixed cells. Membrane defects or discontinuities (of the order of 200–500 A wide) were observed only in prefixed cells which were permeated by ferritin subsequently added. Adjacent prefixed cells which did not become permeated by added ferritin did not reveal any membrane discontinuities. Glutaraldehyde does not per se induce or create such membrane defects since cells which had been fixed by glutaraldehyde before the 10-sec time point or after the 180-sec time point were never permeable to added ferritin, and the cell membranes never contained any defects. It was also observed that early in hemolysis (7–12 sec) a small bulge in one zone of the membrane often occurred. Ghost cells produced by holothurin A (a saponin) and fixed by glutaraldehyde became permeated by ferritin subsequently added, but no membrane discontinuities were seen. Ghosts produced by lysolecithin and fixed by glutaraldehyde also became permeated by subsequently added ferritin, and many membrane defects were seen here (about 300 A wide).
机译:发现铁蛋白和胶体金在快速或渐进性低渗性溶血过程中会渗透人红细胞。只有溶血的细胞含有这些颗粒。相邻的完整细胞不包含示踪剂。低渗溶血开始后3分钟添加的铁蛋白或金没有渗透到已成为暂时可渗透的幽灵细胞中。通过在溶血开始后的不同时间添加铁蛋白,可以确定大多数细胞的渗透状态(或从发展到关闭膜孔之间的间隔)仅在溶血开始后约15到25秒存在。溶血。通过在溶血开始后的10到20秒之间添加戊二醛,可以将暂时的“孔”固定在打开位置。通过添加到这些前缀细胞中的铁蛋白和金的细胞进入来显示这种固定孔的存在。膜缺陷或不连续性(约200–500 A宽)仅在前缀细胞中观察到,随后被铁蛋白渗透。没有被添加的铁蛋白渗透的相邻的带前缀细胞没有发现任何膜不连续性。戊二醛本身不会诱导或产生这种膜缺陷,因为在10秒的时间点之前或180秒的时间点之后被戊二醛固定的细胞从不渗透添加的铁蛋白,并且细胞膜也从未包含任何缺陷。还观察到,在溶血的早期(7-12秒),经常在膜的一个区域出现小隆起。由全硫蛋白A(一种皂苷)产生并由戊二醛固定的鬼细胞随后被铁蛋白渗透,但是没有看到膜的不连续性。由溶血卵磷脂产生并由戊二醛固定的鬼魂也被随后加入的铁蛋白渗透,在此发现许多膜缺陷(约300 A宽)。

著录项

  • 作者

    Seeman, Philip;

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  • 年度 1967
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  • 原文格式 PDF
  • 正文语种 {"code":"en","name":"English","id":9}
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