Alzheimer amyloid protein precursor is localized in nerve terminal preparations to rab5-containing vesicular organelles distinct from those implicated in the synaptic vesicle pathway

Annat F. Ikin, Willem G. Annaert, Kohji Takei, Pietro De Camilli, Reinhard Jahn, Paul Greengard, Joseph D. Buxbaum

Research output: Contribution to journalArticlepeer-review

23 Citations (Scopus)

Abstract

In order to localize amyloid protein precursor (APP) in nerve terminals, we have immunoisolated vesicular organelles from nerve terminal preparations using antibodies to Rab5 and synaptophysin. These immunoisolates were then analyzed by electron microscopy and by immunoblotting. The synaptophysin immunoisolates represented a nearly homogeneous population of small synaptic vesicles, with less than 10% contamination by other organelles, and very little APP. In contrast, Rab5 immunoisolates contained, in addition to small synaptic vesicles, substantial numbers of large uni- and bilamellar vesicles and high levels of APP. Thus, it appears that nerve terminal APP is contained predominantly in large vesicular organelles, distinct from synaptic vesicles and from the synaptic vesicle recycling pathway.

Original languageEnglish
Pages (from-to)31783-31786
Number of pages4
JournalJournal of Biological Chemistry
Volume271
Issue number50
DOIs
Publication statusPublished - 1996
Externally publishedYes

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology

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