Fan J Y, Carpentier J L, Gorden P, Van Obberghen E, Blackett N M, Grunfeld C, Orci L
Proc Natl Acad Sci U S A. 1982 Dec;79(24):7788-91. doi: 10.1073/pnas.79.24.7788.
When 125I-labeled insulin (125I-insulin) is incubated with 3T3-L1 adipocytes and cells processed for electron microscopic autoradiography, the ligand initially localizes preferentially to microvilli and coated pits. As a function of time and temperature, this initial preferential localization to microvilli is lost, and the ligand is internalized by the cell. Serial sections of apparent coated vesicles near the cell surface indicate that about half of these structures are true vesicles and, therefore, intermediates in this receptor-mediated endocytotic process. With time, 125I-insulin localizes to larger intracellular membrane-bounded structures. When cells are incubated with another ligand, cationic ferritin, that is taken up by adsorptive endocytosis, essentially the same structures are involved as for the endocytosis of 125I-insulin. The data suggest that specificity for receptor-mediated endocytosis is conferred by the specific ligand receptor and possibly by ligand-induced receptor mobility in the plane of the plasma membrane. Other structures such as coated pits, coated vesicles, larger vesicles, and secondary lysosomes are common for different ligands.
当用¹²⁵I标记的胰岛素(¹²⁵I - 胰岛素)与3T3 - L1脂肪细胞一起孵育,并对细胞进行电子显微镜放射自显影处理时,配体最初优先定位于微绒毛和被膜小窝。随着时间和温度的变化,这种最初对微绒毛的优先定位消失,配体被细胞内化。细胞表面附近明显的被膜小泡的连续切片表明,这些结构中约一半是真正的小泡,因此是这种受体介导的内吞过程的中间体。随着时间的推移,¹²⁵I - 胰岛素定位于更大的细胞内膜结合结构。当细胞与另一种通过吸附性内吞作用摄取的配体阳离子铁蛋白一起孵育时,参与¹²⁵I - 胰岛素内吞作用的结构基本相同。数据表明,受体介导的内吞作用的特异性是由特定的配体受体赋予的,可能还由配体诱导的受体在质膜平面内的移动性赋予。其他结构,如被膜小窝、被膜小泡、较大的小泡和次级溶酶体,对于不同的配体来说是常见的。