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Endogenous glycosphingolipids move to the cell surface at a rate consistent with bulk flow estimates
W W Young1, M S Lutz, W A Blackburn
1Department of Biological and Biophysical Sciences, University of Louisville, Kentucky 40292.
The Journal of Biological Chemistry
|June 25, 1992
Summary
The bulk flow model of intracellular transport was supported by tracking glycosphingolipids. These lipids rapidly reached the plasma membrane, consistent with bulk flow predictions for cellular transport.
Area of Science:
- Cell Biology
- Molecular Biology
Background:
- The bulk flow model posits that intracellular transport from the ER to the plasma membrane occurs without specific signals.
- This model predicts that endogenous lipid components within transport vesicles move at the rapid rate characteristic of bulk flow.
Purpose of the Study:
- To test the bulk flow model's prediction regarding the transport rate of endogenous lipid components.
- To determine the rate at which glycosphingolipids move from the ER, through the Golgi, to the plasma membrane.
Main Methods:
- Utilized Chinese hamster ovary cells for experiments.
- Employed metabolic labeling with tritiated palmitate.
- Quantified transport rates using periodate oxidation of cell surface ganglioside GM3.
Main Results:
- Radioactive precursor rapidly incorporated into ceramide and glucosyl ceramide.
- Synthesis of lactosyl ceramide and ganglioside GM3 showed delays of 5-6 min and 11-12 min, respectively.
- Labeled GM3 reached the plasma membrane 5-6 min post-synthesis, with total transport time around 18 min from ceramide synthesis.
Conclusions:
- The observed transport rate of glycosphingolipids aligns with bulk flow estimates.
- These findings support the bulk flow model for intracellular trafficking of lipids.
- Lipid transport vesicles move efficiently to the plasma membrane at high speeds.