Abstract
The specific phosphatase inhibitor okadaic acid (OA) induced fragmentation of the Golgi apparatus in interphase HeLa cells. Immunoelectron microscopy for galactosyltransferase identified a major Golgi fragment composed of a cluster of vesicles and tubules that was morphologically indistinguishable from the 'Golgi cluster' previously described in mitotic cells. The presence of homogeneous immunofluorescence staining for galactosyltransferase in OA-treated cells also suggested that isolated Golgi vesicles, previously found in mitotic cells, existed along with the clusters. After removal of OA, both clusters and vesicles appeared to participate in a reassembly pathway that strongly resembled that occurring during telophase. OA also induced inhibition of intracellular transport, another feature of mitotic cells. OA treatment prevented newly synthesised G protein of vesicular stomatitis virus (VSV) from acquiring resistance to endoglycosidase H and from arriving at the cell surface. In addition, fluid phase endocytosis of horseradish peroxidase (HRP) was reduced to less than 10% of control values. All these effects were dose-dependent and reversible. OA should be a useful tool to study the Golgi division and membrane traffic.
Original language | English |
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Pages (from-to) | 753-9 |
Number of pages | 7 |
Journal | Journal of Cell Science |
Volume | 100 ( Pt 4) |
Publication status | Published - Dec 1991 |
Keywords
- Biological Transport
- Endocytosis
- Ethers, Cyclic
- Galactosyltransferases
- Golgi Apparatus
- HeLa Cells
- Horseradish Peroxidase
- Humans
- Interphase
- Ionophores
- Membrane Glycoproteins
- Microscopy, Fluorescence
- Morphogenesis
- Okadaic Acid
- Phosphoprotein Phosphatases
- Viral Envelope Proteins