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

73Citations
Citations of this article
58Readers
Mendeley users who have this article in their library.

This article is free to access.

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.

Cite

CITATION STYLE

APA

Ikin, A. F., Annaert, W. G., Takei, K., De Camilli, P., Jahn, R., Greengard, P., & Buxbaum, J. D. (1996). Alzheimer amyloid protein precursor is localized in nerve terminal preparations to rab5-containing vesicular organelles distinct from those implicated in the synaptic vesicle pathway. Journal of Biological Chemistry, 271(50), 31783–31786. https://doi.org/10.1074/jbc.271.50.31783

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free