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Therond, P.

Publications and source records attributed to Therond, P..

2 recordsLinked to original sources

Arf6 is necessary for high level Wingless signalling during Drosophila wing development

Wnt signalling is a core pathway involved in a wide range of developmental processes throughout the metazoa. In vitro studies have suggested that the small GTP binding protein Arf6 regulates upstream steps of Wnt transduction, by promoting the phosphorylation of the Wnt co-receptor, LRP6, and the release of {beta}-catenin from the adherens junctions. To assess the relevance of these previous findings in vivo, we analyse the consequence of the absence of Arf6 activity on Drosophila wing patterning, a developmental model of Wnt/Wingless signalling. We observed a dominant loss of wing margin bristles and Senseless expression in Arf6 mutant flies, phenotypes characteristic of a defect in high level Wingless signalling. In contrast to previous findings, we show that Arf6 is required downstream of Armadillo/{beta}-catenin stabilisation in Wingless signal transduction. Our data suggest that Arf6 modulates the activity of a downstream nuclear regulator of Pangolin activity in order to control the induction of high level Wingless signalling. Our findings represent a novel regulatory role for Arf6 in Wingless signalling.

developmental biology↗

Hedgehog Signalling Modulates Glial Proteostasis and Lifespan.

The conserved Hedgehog (Hh) signaling pathway has a well-established role in animal development, however its function during adulthood remains largely unknown. Here, we investigated whether the Hh signaling pathway is active during adult life in Drosophila melanogaster and uncovered a protective function for Hh signaling in coordinating correct proteostasis in glial cells. Adult-specific depletion of Hh reduces lifespan, locomotor activity and dopaminergic neuron integrity. Conversely, increased expression of Hh extends lifespan and improves fitness. Moreover, Hh pathway activation in glia rescues the lifespan and age-associated defects of hedgehog (hh) mutants. At the molecular level, the Hh pathway regulates downstream chaperones, principally hsp40 and hsp68, whose overexpression in glial cells rescues the shortened lifespan and proteostasis defects of hh mutants. Finally, we demonstrate the protective ability of Hh signalling in a Drosophila Alzheimers disease model expressing human Amyloid Beta (A{beta}1-42) in the glia. Overall, we propose that Hh signalling is requisite for lifespan determination and correct proteostasis in glial cells and may have potential in ameliorating a wide range of degenerative diseases.

neuroscience↗