RT Journal Article
SR Electronic
T1 Axonal Transport, Amyloid Precursor Protein, Kinesin-1, and the Processing Apparatus: Revisited
JF The Journal of Neuroscience
JO J. Neurosci.
FD Society for Neuroscience
SP 2386
OP 2395
DO 10.1523/JNEUROSCI.3089-04.2005
VO 25
IS 9
A1 Lazarov, Orly
A1 Morfini, Gerardo A.
A1 Lee, Edward B.
A1 Farah, Mohamed H.
A1 Szodorai, Anita
A1 DeBoer, Scott R.
A1 Koliatsos, Vassilis E.
A1 Kins, Stefan
A1 Lee, Virginia M.-Y.
A1 Wong, Philip C.
A1 Price, Donald L.
A1 Brady, Scott T.
A1 Sisodia, Sangram S.
YR 2005
UL http://www.jneurosci.org/content/25/9/2386.abstract
AB The sequential enzymatic actions of β-APP cleaving enzyme 1 (BACE1), presenilins (PS), and other proteins of the γ-secretase complex liberate β-amyloid (Aβ) peptides from larger integral membrane proteins, termed β-amyloid precursor proteins (APPs). Relatively little is known about the normal function(s) of APP or the neuronal compartment(s) in which APP undergoes proteolytic processing. Recent studies have been interpreted as consistent with the idea that APP serves as a kinesin-1 cargo receptor and that PS and BACE1 are associated with the APP-resident membranous cargos that undergo rapid axonal transport. In this report, derived from a collaboration among several independent laboratories, we examined the potential associations of APP and kinesin-1 using glutathione S-transferase pull-down and coimmunoprecipitation assays. In addition, we assessed the trafficking of membrane proteins in the sciatic nerves of transgenic mice with heterozygous or homozygous deletions of APP. In contrast to previous reports, we were unable to find evidence for direct interactions between APP and kinesin-1. Furthermore, the transport of kinesin-1 and tyrosine kinase receptors, previously reported to require APP, was unchanged in axons of APP-deficient mice. Finally, we show that two components of the APP proteolytic machinery, i.e., PS1 and BACE1, are not cotransported with APP in the sciatic nerves of mice. These findings suggest that the hypothesis that APP serves as a kinesin-1 receptor and that the proteolytic processing machinery responsible for generating Aβ is transported in the same vesicular compartment in axons of peripheral nerves requires revision.