Seeman P
J Cell Biol. 1967 Jan;32(1):55-70. doi: 10.1083/jcb.32.1.55.
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).
在快速或逐渐低渗溶血过程中,发现铁蛋白和胶体金可渗透进入人红细胞。只有溶血的细胞含有这些颗粒;相邻的完整细胞不含示踪剂。低渗溶血开始3分钟后添加的铁蛋白或金不会渗透进入已变成瞬时可渗透的空壳细胞。通过在溶血开始后的不同时间添加铁蛋白,确定对于大多数细胞而言,可渗透状态(或膜孔形成和关闭之间的间隔时间)仅在溶血开始后约15至25秒存在。仅在溶血开始后10至20秒之间添加戊二醛,才有可能将瞬时“孔”固定在开放位置。添加到这些预先固定细胞中的铁蛋白和金进入细胞,证明了这种固定孔的存在。仅在随后被添加的铁蛋白渗透的预先固定细胞中观察到膜缺陷或不连续(宽约200 - 500埃)。未被添加的铁蛋白渗透的相邻预先固定细胞未显示任何膜不连续。戊二醛本身不会诱导或产生这种膜缺陷,因为在10秒时间点之前或180秒时间点之后用戊二醛固定的细胞从未对添加的铁蛋白具有渗透性,并且细胞膜从未包含任何缺陷。还观察到在溶血早期(7 - 12秒),膜的一个区域经常出现一个小凸起。由海参毒素A(一种皂角苷)产生并用戊二醛固定的空壳细胞会被随后添加的铁蛋白渗透,但未观察到膜不连续。由溶血卵磷脂产生并用戊二醛固定的空壳细胞也会被随后添加的铁蛋白渗透,并且在此处观察到许多膜缺陷(宽约300埃)。