Ethanol perturbs the secretory pathway in astrocytes

Neurobiol Dis. 2005 Dec;20(3):773-84. doi: 10.1016/j.nbd.2005.05.012. Epub 2005 Jun 13.

Abstract

Ethanol exposure induces retention of glycoproteins in growing astrocytes. We examined the intracellular sites at which this retention occurs and investigated whether this effect is accompanied by alterations in the Golgi complex and microtubular system. We studied the effects of ethanol on the Golgi complex structure, as well as on the secretory pathway functionality by monitoring both the transport of the VSV-G protein and the protein levels of several molecules involved in the regulation of this pathway. Ethanol was found to delay VSV-G transport, modify Golgi complex morphology, and reduce the number of secretory vesicles. Moreover, ethanol affected the levels of mannosidase II, p58, betaCOP, rbet1, and several Rab GTPases. It also affected microtubule organization and polymerization and the levels of the motor proteins kinesin and dynein. Most of these effects were dose-dependent. These alterations, together with those previously reported concerning biosynthesis of glycoconjugates, provide novel insights into how ethanol impairs brain development.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alcohol-Induced Disorders, Nervous System / metabolism
  • Alcohol-Induced Disorders, Nervous System / physiopathology
  • Animals
  • Astrocytes / drug effects*
  • Astrocytes / metabolism
  • Brain / drug effects*
  • Brain / growth & development*
  • Brain / physiopathology
  • Cells, Cultured
  • Coatomer Protein / drug effects
  • Coatomer Protein / metabolism
  • Dose-Response Relationship, Drug
  • Ethanol / toxicity*
  • Female
  • Fetal Alcohol Spectrum Disorders / metabolism
  • Fetal Alcohol Spectrum Disorders / physiopathology
  • Golgi Apparatus / drug effects*
  • Golgi Apparatus / metabolism
  • Mannose-Binding Lectins / drug effects
  • Mannose-Binding Lectins / metabolism
  • Mannosidases / drug effects
  • Mannosidases / metabolism
  • Membrane Proteins / drug effects
  • Membrane Proteins / metabolism
  • Microtubules / drug effects
  • Microtubules / metabolism
  • Molecular Motor Proteins / drug effects
  • Molecular Motor Proteins / metabolism
  • Pregnancy
  • Prenatal Exposure Delayed Effects / metabolism
  • Prenatal Exposure Delayed Effects / physiopathology
  • Qc-SNARE Proteins / drug effects
  • Qc-SNARE Proteins / metabolism
  • Rats
  • Secretory Vesicles / drug effects
  • Secretory Vesicles / metabolism
  • Signal Transduction / drug effects
  • Signal Transduction / physiology
  • Vesicular Transport Proteins / drug effects
  • Vesicular Transport Proteins / metabolism
  • rab GTP-Binding Proteins / drug effects
  • rab GTP-Binding Proteins / metabolism

Substances

  • BET1 protein, rat
  • Coatomer Protein
  • LMAN1 protein, human
  • Mannose-Binding Lectins
  • Membrane Proteins
  • Molecular Motor Proteins
  • Qc-SNARE Proteins
  • Vesicular Transport Proteins
  • Ethanol
  • Mannosidases
  • mannosyl-oligosaccharide 1,3 - 1,6-alpha-mannosidase
  • rab GTP-Binding Proteins