Studies on the neuronal Golgi apparatus-complex. I. Quantitative ultrastructural autoradiographic analysis of the endocytosis into the Golgi complex of wheat germ agglutinin by cultured murine neuroblastoma cells. II. Identification of a 160 Kd polypeptide of the medial cisterns of the Golgi complex
An ultrastructural autoradiographic method is presented which quantitates the sequential endocytosis of tritiated wheat germ agglutinin (N-(acetyl-/sup 3/H)-WGA) into the Golgi complex and lysosomes of cultured murine neuroblastoma cells. Cells were incubated with /sup 3/H-WGA for one hour at 4/sup 0/C, washed and incubated in complete medium without ligand at 37/sup 0/C for 5, 15, 30, and 120 minutes. At 15 minutes, the optimized sources/..mu..m/sup 2/ of neuroblastoma cell area, which represented the grain density of each compartment, were: Golgi associated vesicles, i.e. clusters of vesicles within a one micron radius of the Golgi cisterns, (1.41 + -0.28), Golgi cisterns (0.73 + -0.41), lysosomes (0.1 + -0.09); at two hours, Golgi associated vesicles exhibited some labeling ((0.71 + -0.1), while 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 /sup 3/H-WGA into lysosomes, or that it constitutes part of a separate and quantitatively significant pathway of endocytosis of this ligand.
- Research Organization:
- Pennsylvania Univ., Philadelphia (USA)
- OSTI ID:
- 6998027
- Resource Relation:
- Other Information: Thesis (Ph. D.)
- Country of Publication:
- United States
- Language:
- English
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AGGLUTININS
MOLECULAR STRUCTURE
PHAGOCYTOSIS
AUTORADIOGRAPHY
CELL CONSTITUENTS
LYSOSOMES
MICE
NERVE CELLS
POLYPEPTIDES
TRITIUM COMPOUNDS
TUMOR CELLS
ANIMAL CELLS
ANIMALS
ANTIBODIES
LABELLED COMPOUNDS
MAMMALS
ORGANIC COMPOUNDS
ORGANOIDS
PEPTIDES
PROTEINS
RODENTS
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VERTEBRATES
550201* - Biochemistry- Tracer Techniques