Frizzled-5 Receptor Is Involved in Neuronal Polarity and Morphogenesis of Hippocampal Neurons
Author
dc.contributor.author
Slater, Paula G.
Author
dc.contributor.author
Ramírez, Valerie T.
es_CL
Author
dc.contributor.author
González Billault, Christian
es_CL
Author
dc.contributor.author
Varela Nallar, Lorena
es_CL
Author
dc.contributor.author
Inestrosa, Nibaldo C.
es_CL
Admission date
dc.date.accessioned
2014-01-08T20:44:04Z
Available date
dc.date.available
2014-01-08T20:44:04Z
Publication date
dc.date.issued
2013
Cita de ítem
dc.identifier.citation
PLoS ONE 8(10): e78892
en_US
Identifier
dc.identifier.other
doi:10.1371/journal.pone.0078892
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/119666
General note
dc.description
Artículo de publicación ISI
en_US
Abstract
dc.description.abstract
The Wnt signaling pathway plays important roles during different stages of neuronal development, including neuronal
polarization and dendritic and axonal outgrowth. However, little is known about the identity of the Frizzled receptors
mediating these processes. In the present study, we investigated the role of Frizzled-5 (Fzd5) on neuronal
development in cultured Sprague-Dawley rat hippocampal neurons. We found that Fzd5 is expressed early in
cultured neurons on actin-rich structures localized at minor neurites and axonal growth cones. At 4 DIV, Fzd5
polarizes towards the axon, where its expression is detected mainly at the peripheral zone of axonal growth cones,
with no obvious staining at dendrites; suggesting a role of Fzd5 in neuronal polarization. Overexpression of Fzd5
during the acquisition of neuronal polarity induces mislocalization of the receptor and a loss of polarized axonal
markers. Fzd5 knock-down leads to loss of axonal proteins, suggesting an impaired neuronal polarity. In contrast,
overexpression of Fzd5 in neurons that are already polarized did not alter polarity, but decreased the total length of
axons and increased total dendrite length and arborization. Fzd5 activated JNK in HEK293 cells and the effects
triggered by Fzd5 overexpression in neurons were partially prevented by inhibition of JNK, suggesting that a noncanonical
Wnt signaling mechanism might be involved. Our results suggest that, Fzd5 has a role in the establishment
of neuronal polarity, and in the morphogenesis of neuronal processes, in part through the activation of the noncanonical
Wnt mechanism involving JNK.