AP-1/sigma1B-adaptin mediates endosomal synaptic vesicle recycling, learning and memory

EMBO J. 2010 Apr 21;29(8):1318-30. doi: 10.1038/emboj.2010.15. Epub 2010 Mar 4.

Abstract

Synaptic vesicle recycling involves AP-2/clathrin-mediated endocytosis, but it is not known whether the endosomal pathway is also required. Mice deficient in the tissue-specific AP-1-sigma1B complex have impaired synaptic vesicle recycling in hippocampal synapses. The ubiquitously expressed AP-1-sigma1A complex mediates protein sorting between the trans-Golgi network and early endosomes. Vertebrates express three sigma1 subunit isoforms: A, B and C. The expressions of sigma1A and sigma1B are highest in the brain. Synaptic vesicle reformation in cultured neurons from sigma1B-deficient mice is reduced upon stimulation, and large endosomal intermediates accumulate. The sigma1B-deficient mice have reduced motor coordination and severely impaired long-term spatial memory. These data reveal a molecular mechanism for a severe human X-chromosome-linked mental retardation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Protein Complex 1 / analysis
  • Adaptor Protein Complex 1 / genetics
  • Adaptor Protein Complex 1 / metabolism*
  • Animals
  • Behavior, Animal
  • Cells, Cultured
  • Clathrin / metabolism
  • Endosomes / metabolism*
  • Female
  • Gene Expression
  • Hippocampus / cytology
  • Humans
  • Learning*
  • Memory*
  • Mice
  • Mice, Knockout
  • Motor Activity
  • Neurons / metabolism
  • Protein Isoforms / analysis
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism
  • Synaptic Vesicles / metabolism*

Substances

  • Adaptor Protein Complex 1
  • Clathrin
  • Protein Isoforms