Santini M T, Indovina P L, Simmons J R, Peterson S W
Laboratorio di Ultrastrutture, Università di Napoli, Rome, Italy.
Biochim Biophys Acta. 1990 Sep 24;1054(3):333-6. doi: 10.1016/0167-4889(90)90105-m.
Insulin receptor internalization in response to insulin incubation (down-regulation) has been shown to occur in human erythrocytes as well as in human erythrocyte ghosts. It is also known that changes in cell membrane events can be detected with electron paramagnetic resonance (EPR) spectroscopy using spin labels. In the present study, changes in erythrocyte membrane order during down regulation as measured by the 2T'II parameter were investigated using EPR. The spin label, 5-nitroxystearate, which inserts into the lipid bilayer of cell membranes, was used. Changes in 2T'II at 37 degrees C were followed over a 3 h time period. A transient decrease in erythrocyte membrane order began within 30 min of the start of insulin incubation and reached a minimum level of 52.5 Gauss (G) within 90 min. This represented nearly a 2 G decrease from the zero incubation time value. Membrane order returned to the initial value by 2.5 h. These time-related changes in membrane order corresponded well with the insulin receptor internalization process as followed by surface binding assays. Surface insulin binding began to decrease within 30 min of the start of insulin incubation, and was reduced to 30% of control values within 2 h. Similar correlations between membrane order and receptor internalization were observed at 23 degrees C. Erythrocytes incubated with denatured insulin, and ATP-depleted erythrocytes incubated with native insulin, did not down-regulate their insulin receptors. Under these conditions, these erythrocytes also did not exhibit the transient decreases in membrane order. These findings are consistent with the hypothesis that an increase in membrane disorder is part of the mechanism of insulin receptor down-regulation.
胰岛素孵育后胰岛素受体内化(下调)已被证明在人红细胞以及人红细胞影中都会发生。还已知细胞膜事件的变化可用电子顺磁共振(EPR)光谱结合自旋标记进行检测。在本研究中,使用EPR研究了下调过程中红细胞膜有序性的变化,该变化通过2T'II参数测量。使用了插入细胞膜脂质双层的自旋标记5 - 硝基硬脂酸盐。在37摄氏度下,在3小时的时间段内跟踪2T'II的变化。胰岛素孵育开始后30分钟内,红细胞膜有序性开始短暂下降,并在90分钟内达到最低水平52.5高斯(G)。这比零孵育时间的值下降了近2 G。膜有序性在2.5小时时恢复到初始值。这些与时间相关的膜有序性变化与表面结合测定所跟踪的胰岛素受体内化过程非常吻合。胰岛素孵育开始后30分钟内,表面胰岛素结合开始下降,并在2小时内降至对照值的30%。在23摄氏度下也观察到膜有序性与受体内化之间的类似相关性。用变性胰岛素孵育的红细胞以及用天然胰岛素孵育的ATP耗尽的红细胞,其胰岛素受体未下调。在这些条件下,这些红细胞也未表现出膜有序性的短暂下降。这些发现与膜无序性增加是胰岛素受体下调机制的一部分这一假设一致。