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

H J McLauchlan, J James, J M Lucocq, S Ponnambalam

Research output: Contribution to journalArticlepeer-review

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.
Original languageEnglish
Pages (from-to)705-13
Number of pages9
JournalInternational Journal of Biochemistry and Cell Biology
Volume25
Issue number8
DOIs
Publication statusPublished - 2001

Keywords

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

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