Marshall S
J Biol Chem. 1985 Nov 5;260(25):13517-23.
Based on the distribution of 125I-insulin between the cell surface and the cell interior, it was found that insulin rapidly binds (t 1/2 = 0.4 min) to surface receptors at 37 degrees C, and after an initial lag period of about 1 min, accumulates intracellularly until steady state is reached (t 1/2 = 3.5 min). At this time about 40% of the total cell-associated 125I-insulin resides in the cell interior reflecting a dynamic equilibrium between the rate of insulin endocytosis and the rate at which internalized insulin is processed and extruded from cells. Since this percentage decreased to 15% at 16 degrees C, it appears that internalization is more temperative-sensitive than the intracellular processing of insulin. When 125I-insulin was preloaded into the cell interior, it was found that internalized insulin was rapidly released to the medium at 37 degrees C (t 1/2 = 6.5 min) and consisted of both degraded products and intact insulin (as assessed by trichloroacetic acid precipitability and column chromatography). Since 75% of internalized insulin was ultimately degraded, and 25% was released intact, this indicates that degradation is the predominant pathway. To determine when incoming insulin enters a degradative compartment, cells were continually exposed to 125I-insulin and the composition of insulin in the cell interior over time was assessed. After 2 min all endocytosed insulin was intact, between 2-3 min degradation products began accumulating intracellularly, and by 15 min equilibrium was reached with 20% of internalized insulin consisting of degraded products. Degraded insulin was then released from the cell interior within 4-5 min after endocytotic uptake, since this was the earliest time chloroquine was found to inhibit the release of degradation products. Moreover, the final release of degraded insulin was not inhibitable by the energy depleter dinitrophenol. Thus, within the degradative pathway, insulin enters lysosomes by 2.5-3 min and is released to the medium by simple diffusion after an additional 1.5-2 min.
根据125I标记胰岛素在细胞表面和细胞内部的分布情况,发现胰岛素在37℃时能迅速与表面受体结合(t1/2 = 0.4分钟),在大约1分钟的初始延迟期后,在细胞内积累直至达到稳态(t1/2 = 3.5分钟)。此时,与细胞相关的125I标记胰岛素总量中约40%存在于细胞内部,这反映了胰岛素内吞速率与内化胰岛素被细胞处理和排出的速率之间的动态平衡。由于该百分比在16℃时降至15%,似乎内化过程比胰岛素的细胞内加工过程对温度更敏感。当将125I标记胰岛素预先加载到细胞内部时,发现内化胰岛素在37℃时迅速释放到培养基中(t1/2 = 6.5分钟),且包括降解产物和完整胰岛素(通过三氯乙酸沉淀性和柱色谱法评估)。由于75%的内化胰岛素最终被降解,25%完整释放,这表明降解是主要途径。为了确定进入的胰岛素何时进入降解区室,细胞持续暴露于125I标记胰岛素,并随时间评估细胞内部胰岛素的组成。2分钟后,所有内吞的胰岛素都是完整的,在2 - 3分钟之间降解产物开始在细胞内积累,到15分钟时达到平衡,内化胰岛素的20%由降解产物组成。降解的胰岛素在内吞摄取后4 - 5分钟内从细胞内部释放,因为这是最早发现氯喹能抑制降解产物释放的时间。此外,降解胰岛素的最终释放不受能量消耗剂二硝基苯酚的抑制。因此,在降解途径中,胰岛素在2.5 - 3分钟内进入溶酶体,并在再过1.5 - 2分钟后通过简单扩散释放到培养基中。