Carpentier J L, Fehlmann M, Van Obberghen E, Gorden P, Orci L
Biochimie. 1985 Oct-Nov;67(10-11):1143-5. doi: 10.1016/s0300-9084(85)80112-7.
Using a 125I-photoreactive insulin analogue that can be covalently coupled to its receptor we have shown that in rat hepatocytes the insulin receptor is concomitantly internalized with the labeled hormone and afterwards is progressively recycled back to the cell surface. In the course of the internalization process the insulin-receptor complex associates with clear vesicles and later on with lysosomes from which it is recycled through clear vesicles. On the basis of these observations it is suggested that modulation of the rates of internalization and of recycling of the insulin receptor can regulate the number of available surface insulin receptors. This hypothesis is supported by the results of experiments showing that monensin, an inhibitor of receptor recycling enhances insulin induced loss of its own surface receptors (down regulation) in U-937 monocytes.
使用一种可与胰岛素受体共价偶联的¹²⁵I光反应性胰岛素类似物,我们已经证明,在大鼠肝细胞中,胰岛素受体与标记的激素同时内化,随后逐渐循环回到细胞表面。在内化过程中,胰岛素-受体复合物先与清亮小泡结合,随后与溶酶体结合,并通过清亮小泡从中循环。基于这些观察结果,有人提出,调节胰岛素受体的内化和循环速率可以调节可用的表面胰岛素受体数量。这一假说得到了实验结果的支持,这些实验表明,莫能菌素(一种受体循环抑制剂)可增强胰岛素诱导的U-937单核细胞自身表面受体的丧失(下调)。