Unknown

Dataset Information

0

Amyloid precursor protein regulates netrin-1-mediated commissural axon outgrowth.


ABSTRACT: The multifunctional protein netrin-1 was initially discovered as the main attractive cue for commissural axon guidance by acting through its receptor DCC. Recently, we have shown that netrin-1 also interacts with the orphan transmembrane receptor amyloid precursor protein (APP). APP is cleaved by proteases, generating amyloid-? peptide, the main component of the amyloid plaques that are associated with Alzheimer disease. Our previous work demonstrated that via its interaction with APP, netrin-1 is a negative regulator of amyloid-? production in adult brain, but the biological relevance of APP/netrin-1 interaction under non-pathological conditions was unknown. We show here that during commissural axon navigation, APP, expressed at the growth cone, is part of the DCC receptor complex mediating netrin-1-dependent axon guidance. APP interacts with DCC in the presence of netrin-1 and enhances netrin-1-mediated DCC intracellular signaling, such as MAPK activation. Inactivation of APP in mice is associated with reduced commissural axon outgrowth. Thus, APP functionally acts as a co-receptor for DCC to mediate axon guidance.

SUBMITTER: Rama N 

PROVIDER: S-EPMC3436182 | biostudies-other | 2012 Aug

REPOSITORIES: biostudies-other

altmetric image

Publications

Amyloid precursor protein regulates netrin-1-mediated commissural axon outgrowth.

Rama Nicolas N   Goldschneider David D   Corset Véronique V   Lambert Jérémy J   Pays Laurent L   Mehlen Patrick P  

The Journal of biological chemistry 20120710 35


The multifunctional protein netrin-1 was initially discovered as the main attractive cue for commissural axon guidance by acting through its receptor DCC. Recently, we have shown that netrin-1 also interacts with the orphan transmembrane receptor amyloid precursor protein (APP). APP is cleaved by proteases, generating amyloid-β peptide, the main component of the amyloid plaques that are associated with Alzheimer disease. Our previous work demonstrated that via its interaction with APP, netrin-1  ...[more]

Similar Datasets

| S-EPMC3029320 | biostudies-literature
| S-EPMC2757418 | biostudies-literature
| S-EPMC3335837 | biostudies-literature
| S-EPMC4813483 | biostudies-literature
| S-EPMC2650370 | biostudies-literature
| S-EPMC5438598 | biostudies-literature
| S-EPMC2759694 | biostudies-literature
| S-EPMC3024975 | biostudies-literature
| S-EPMC8795569 | biostudies-literature
| S-EPMC2120404 | biostudies-other