ENDOCYTOSIS OF WHEAT-GERM-AGGLUTININ BINDING-SITES FROM THE CELL-SURFACE INTO A TUBULAR ENDOSOMAL NETWORK

By using fluorescence and electron microscopy, the endocytic pathway encountered by cell surface components after they had bound wheat germ agglutinin (WGA) was visualized. The majority of these components are thought to consist of sialylated glycoproteins (HMWAG) that represent a subpopulation of the total cell surface proteins but most of the externally disposed plasma membrane proteins of the cell. Examination of semi‐thin sections by medium‐ and high‐voltage electron microscopy revealed the three‐dimensional organization of vesicular and tubular endosomes. Binding of either fluorescein isothiocyanate‐, horseradish peroxidase‐, or ferritin‐conjugated WGA to cells at 4°C showed that the HMWAG were distributed uniformly over the cell surface. Warming of surface‐labeled cells to 37°C resulted in the endocytosis of WGA into peripheral endo‐somes via invagination of regions of both coated and uncoated membrane. The peripheral endosome appeared as isolated complexes comprising a vesicular element (300‐400 nm diam.) surrounded by and continuous with tubular cister‐nae (45‐60 nm diam.), which did not interconnect the endosomes. After 30 min or more label also became localized in a network of anastomosing tubules (45‐60 nm diam.) that were located in the centrosomal region of the cell. Endocytosed WGA‐HMWAG complexes did not become associated with cisternae of the Golgi apparatus, although tubular and vesicular endosomes were noted in the vicinity of the trans‐Golgi region. The accumulation of WGA‐HMWAG in the endosomes within the centrosomal region was inhibited when cells were incubated at 18°C. None of these compartments contained acid phosphatase activity, a result that is consistent with other data that the HMWAG do not pass through lysosomes initially. The kinetics of labeling were consistent with the interpretation that recycling of most of the WGA binding surface glycoproteins occurred rapidly from early peripheral endosomes followed by the late trans‐Golgi compartment. In conclusion, a portion of cell surface glycoproteins are routed to a complex arrangement of tubular and vesicular compartments following endocytosis that includes a putative post‐endosomal, tubular reticulum that appears to be separate from the trans‐most Golgi saccule. Copyright © 1990 Wiley‐Liss, Inc.