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Goncalves, R. M.

Publications and source records attributed to Goncalves, R. M..

2 recordsLinked to original sources

Neuronal sex identity shapes social buffering of defensive freezing behaviour in fruit flies

Sex differences are pervasive across the animal kingdom1,2, shaped by reproductive strategies, ecological roles, and physiological demands. Neurobiological studies have largely focused on sex differences in reproduction and aggression3,4, leaving understudied how sex shapes other survival-relevant behaviours such as responses to predatory threats. Previous work in vertebrates uncovered sex differences in individual defence responses deployed by rats5 and in social modulation of freezing responses in zebrafish6. The origin of these differences and their potential underlying neuronal circuitry remain however unknown. Here we characterise defensive responses to a visual threat of female and male fruit flies tested alone and in groups. Individually, defensive responses are comparable across sex, with similar freezing levels and moderately increased escape responses in males. In groups, however, we uncovered strong sex differences in freezing as males show consistently shorter freezing bouts, reflecting a stronger social buffering effect than in females. Using a generalised linear mixed model, we demonstrate that the shorter freezes of male flies, when tested in groups, are not explained by well-known locomotor differences between sexes7,8. Although males move more and faster, generating stronger social motion cues that mediate the "safety in numbers" effect in female flies9,10, their response to the surrounding motion is not increased. We further identify the nervous system as the source of this sex-dimorphic behaviour by feminising males through pan-neuronal ectopic expression of transformer, a key regulator of the cell-autonomous sex-differentiation pathway. Finally, we ruled out the visual projection neurons, lobula columnar neurons 11 (LC11), detectors of social motion10, as the source of the neuronal-sex differences observed. This study identifies a neuronal origin of sex differences in socially modulated behaviour that extends beyond sex-specific behavioural modules or locomotor function, important to understand differential impact on survival upon threat across sexes.

neuroscience↗

Targeting activated IL-23 signaling in Scleroderma by tildrakizumab

The pathogenesis of systemic sclerosis (SSc) involves immune system dysregulation and progressive multi-organ fibrosis. Aberrant interleukin-23 (IL-23) function is linked to many inflammatory conditions. Tildrakizumab, a humanized monoclonal antibody that binds to the p19 subunit of IL-23 to block its interaction with the IL-23 receptor, is FDA-approved for treating psoriasis. IL-23 levels are increased in SSc patients with lung involvement, but the pathogenic role of IL-23 in SSc fibrosis remains unclear. We examined IL-23 expression in SSc skin biopsies and assessed the effects of IL-23 inhibition in an in vivo fibrosis model. We found increased IL-23 expression in SSc compared to healthy skin biopsies. Pharmacological blockade of IL-23 signaling using tildrakizumab reversed experimental skin and lung fibrosis. Our findings support a pathogenic role of IL-23 in SSc and suggest that tildrakizumab could be a novel antifibrotic treatment strategy for SSc and related fibrotic disorders. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=162 SRC="FIGDIR/small/701821v1_ufig1.gif" ALT="Figure 1"> View larger version (37K): org.highwire.dtl.DTLVardef@777c8aorg.highwire.dtl.DTLVardef@9163f5org.highwire.dtl.DTLVardef@1399a54org.highwire.dtl.DTLVardef@c30ec2_HPS_FORMAT_FIGEXP M_FIG C_FIG

immunology↗