Axonal remodeling and synaptic differentiation in the cerebellum is regulated by WNT-7a signaling.

Abstract:

:Synapse formation requires changes in cell morphology and the upregulation and localization of synaptic proteins. In the cerebellum, mossy fibers undergo extensive remodeling as they contact several granule cells and form complex, multisynaptic glomerular rosettes. Here we show that granule cells secrete factors that induce axon and growth cone remodeling in mossy fibers. This effect is blocked by the WNT antagonist, sFRP-1, and mimicked by WNT-7a, which is expressed by granule cells. WNT-7a also induces synapsin I clustering at remodeled areas of mossy fibers, a preliminary step in synaptogenesis. Wnt-7a mutant mice show a delay in the morphological maturation of glomerular rosettes and in the accumulation of synapsin I. We propose that WNT-7a can function as a synaptogenic factor.

journal_name

Cell

journal_title

Cell

authors

Hall AC,Lucas FR,Salinas PC

doi

10.1016/s0092-8674(00)80689-3

subject

Has Abstract

pub_date

2000-03-03 00:00:00

pages

525-35

issue

5

eissn

0092-8674

issn

1097-4172

pii

S0092-8674(00)80689-3

journal_volume

100

pub_type

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