Abstract

Author SummaryWnt Planar Cell Polarity (PCP) signaling is a universal regulator of polarity in epithelial cells, but in neurons it regulates axon outgrowth, suggesting the existence of axonal modulators of Wnt-PCP activity. The Amyloid Precursor Proteins (APPs) are intensely investigated because of their link to Alzheimer's disease (AD). APP's in vivo function in the brain and the mechanisms underlying it remain unclear and controversial. In the present work we investigate the role of the Drosophila neuron-specific APP homologue, called APPL, during brain development. We find that APPL is required for the development of αβ neurons in the mushroom body, a structure critical for learning and memory. We find that APPL is a modulator of the Wnt-PCP pathway required for axonal outgrowth, but not for cell polarity. Molecularly, both human APP and fly APPL are found in membrane complexes with PCP receptors. Moreover, we show that APPL regulates PCP pathway activation through its downstream effector Abelson kinase (Abl), which modulates the phosphorylation of the Wnt adaptor protein Dishevelled (Dsh) and the subsequent activation of Wnt-PCP signaling. Taken together our data suggest that APPL is the first example of a neuron-specific modulator of the Wnt-PCP pathway.

Highlights

  • The Wnt Planar Cell Polarity (PCP) pathway is a highly conserved regulator of cellular orientation within the plane of an epithelium [1,2]

  • In the present work we investigate the role of the Drosophila neuron-specific Amyloid Precursor Protein (APP) homologue, called APP Like (APPL), during brain development

  • We find that APPL is a modulator of the Wnt-PCP pathway required for axonal outgrowth, but not for cell polarity

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Summary

Introduction

The Wnt Planar Cell Polarity (PCP) pathway is a highly conserved regulator of cellular orientation within the plane of an epithelium [1,2]. APP is the subject of intense research because of genetic and biochemical links to Alzheimer’s disease (AD), whereby the proteolytic processing of APP generates the Amyloid Beta peptide whose accumulation in the brain is widely thought to induce neurodegeneration [9,10,11,12]. Despite these efforts, the normal physiological function of APP in vivo in the nervous system remains elusive and highly controversial. Another in vivo report, based mainly on gain of function

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