Quantitative ultrastructural, autoradiographic evidence for the magnitude and early involvement of the Golgi apparatus complex in the endocytosis of wheat germ agglutinin by cultured neuroblastoma

Several ligands undergo endocytosis into the Golgi apparatus. We have examined with a quantitative ultrastructural, autoradiographic method the sequential endocytosis of tritiated wheat germ agglutinin ( 3 H‐WGA) by cultured murine neuroblastoma cells. Cells were incubated with 3 H‐WGA for 1 hour at 4°C, washed, and incubated in complete medium without ligand at 37°C for 5, 15, 30, and 120 minutes. At 5 minutes, the optimized sources/μm 2 of neuroblastoma cell area, which represented the grain density of each compartment, were as follows: smooth vesicles and tubules, 1.03 ± 0.88; Golgi‐associated vesicles, i.e., clusters of vesicles within a 1 μm radius of the Golgi cisterns, 1.03 ± 0.31; Golgi cisterns, < 0.01; and lysosomes, 0.26 ± 0.16. At 15 minutes grain densities were: smooth vesicles and tubules, 0.9 ± 0.34; Golgi‐associated vesicles, 1.41 ± 0.28; Golgi cisterns, 0.73 ± 0.41; and lysosomes, 0.1 ± 0.09. At 30 minutes grain densities were: smooth vesicles and tubules, 0.46 ± 0.46; Golgi‐associated vesicles, 1.78 ± 0.34; Golgi cisterns, 0.89 ± 0.78; and lysosomes, 0.39 ± 0.14. At 2 hours, smooth vesicles, tubules, and Golgi cisterns were not labeled, Golgi‐associated vesicles were still labeled (0.71 ± 0.1), and lysosomes were heavily labeled (2.17 ± 0.22). These results are consistent with the hypotheses that either the Golgi complex (cisterns and associated vesicles) is an early and intermediate step of the endocytosis of 3 H‐WGA into lysosomes or that it constitutes part of a separate and quantitatively significant pathway of endocytosis of this ligand.