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Characterization of Endocytic Pathways by Quantitative Fluorescence Microscopy

Published online by Cambridge University Press:  02 July 2020

Frederick R. Maxfield
Affiliation:
Department of Biochemistry, Cornell University Medical College, 1300 York Avenue, New York, NY10021
Richik N. Ghosh
Affiliation:
Department of Biochemistry, Cornell University Medical College, 1300 York Avenue, New York, NY10021
William G. Mallet
Affiliation:
Department of Biochemistry, Cornell University Medical College, 1300 York Avenue, New York, NY10021
Thwe Thwe Soe
Affiliation:
Department of Biochemistry, Cornell University Medical College, 1300 York Avenue, New York, NY10021
Philip L. Leopold
Affiliation:
Department of Biochemistry, Cornell University Medical College, 1300 York Avenue, New York, NY10021
Leona Cohen-Gould
Affiliation:
Department of Biochemistry, Cornell University Medical College, 1300 York Avenue, New York, NY10021
Satyajit Mayor
Affiliation:
National Centre for Biological Sciences, Tata Institute for Fundamental Research, P.O. Box 1234, Indian Institute of Science Campus, Bangalore560 012, India
Sushmita Mukherjee
Affiliation:
Department of Biochemistry, Cornell University Medical College, 1300 York Avenue, New York, NY10021
Xiaohui Zha
Affiliation:
Department of Biochemistry, Cornell University Medical College, 1300 York Avenue, New York, NY10021
Timothy E. McGraw
Affiliation:
Department of Biochemistry, Cornell University Medical College, 1300 York Avenue, New York, NY10021
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Extract

We have used light and electron microscopy to analyze endocytic trafficking pathways. In one set of studies, we have used fluorescently labeled antibodies to trace an endocytic pathway from the cell surface to the trans- Golgi network (TGN). Cells were transfected with a construct consisting of the transmembrane and cytoplasmic domains of TGN38 and the extracellular domain of Tac. TGN38 is predominantly in the TGN, but a small fraction is found on the cell surface. We used FITC-labeled anti-Tac monoclonal IgG to analyze the pathway from the surface to the TGN. We compared the distribution of internalized Tac-TGN38 to internalized transferrin. We found that most Tac-TGN38 enters the same early endosomes as transferrin. Furthermore, most Tac-TGN38 returns to the cell surface from the endocytic recycling compartment (ERC) at the same rate as transferrin. However, on each pass through the cell approximately 18% of Tac-TGN is retained, and this Tac-TGN38 is delivered to the TGN.

Type
Dynamics of Cellular Membrane Traffic
Copyright
Copyright © Microscopy Society of America

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References

Mukherjee, S. et al., Endocytosis, Physiological Reviews 77(1997)759.CrossRefGoogle Scholar