Characterization and regulation of constitutive transport intermediates involved in trafficking from the trans-Golgi network

Cell Biol Int. 2001;25(8):705-13. doi: 10.1006/cbir.2001.0717.

Abstract

Transport vesicles or containers (TCs) mediate constitutive protein transport between the trans-Golgi network (TGN) and the plasma membrane. A key question is the nature and regulation of these transport containers or intermediates. We have used a trans-Golgi network resident, TGN38, to investigate TC formation. TGN38 is a recycling membrane glycoprotein that moves to the cell surface via constitutive membrane traffic and returns via the endosomal pathway. An in vitro assay to measure TC formation was devised using rat liver Golgi membranes, cytosolic factors and ATP. Transport intermediates containing TGN38 were produced and found to be smooth vesicles and tubules of up to 200 nm in length. These membrane-enclosed structures contain different constitutively secreted membrane glycoproteins, including molecules involved in immune functions such as MHC Class I and the polymeric Ig receptor, showing that these intermediates correspond to TCs that have been previously identified in vivo. Importantly, TC formation can be stimulated or inhibited by protein kinase and phosphatase inhibitors, showing regulation by intracellular signalling pathways.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biological Transport / drug effects
  • Biological Transport / physiology*
  • Brain / metabolism
  • Cattle
  • Cytosol / metabolism
  • Dose-Response Relationship, Drug
  • Glycoproteins*
  • Golgi Apparatus / drug effects
  • Golgi Apparatus / metabolism*
  • Golgi Apparatus / ultrastructure
  • Guanosine 5'-O-(3-Thiotriphosphate) / pharmacology
  • Intracellular Membranes / drug effects
  • Intracellular Membranes / metabolism
  • Intracellular Membranes / ultrastructure
  • Liver / ultrastructure
  • Membrane Glycoproteins / metabolism
  • Membrane Proteins*
  • Microscopy, Immunoelectron
  • N-Acetyllactosamine Synthase / metabolism
  • Okadaic Acid / pharmacology
  • Rats

Substances

  • Glycoproteins
  • Membrane Glycoproteins
  • Membrane Proteins
  • Tgoln2 protein, rat
  • Okadaic Acid
  • Guanosine 5'-O-(3-Thiotriphosphate)
  • N-Acetyllactosamine Synthase