Adverse impact of female reproductive signaling on age-dependent neurodegeneration after mild head trauma in Drosophila

Environmental insults, including mild head trauma, significantly increase the risk of neurodegeneration. However, it remains challenging to establish a causative connection between early-life exposure to mild head trauma and late-life emergence of neurodegenerative deficits, nor do we know how sex and age compound the outcome. Using a Drosophila model, we demonstrate that exposure to mild head trauma causes neurodegenerative conditions that emerge late in life and disproportionately affect females. Increasing age-at-injury further exacerbates this effect in a sexually dimorphic manner. We further identify sex peptide signaling as a key factor in female susceptibility to post-injury brain deficits. RNA sequencing highlights a reduction in innate immune defense transcripts specifically in mated females during late life. Our findings establish a causal relationship between early head trauma and late-life neurodegeneration, emphasizing sex differences in injury response and the impact of age-at-injury. Finally, our findings reveal that reproductive signaling adversely impacts female response to mild head insults and elevates vulnerability to late-life neurodegeneration.

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Publication Details

Journal
eLife
Published
2024-08-30
DOI
https://doi.org/10.7554/elife.97908.3
Citations
3
Primary Topic
Genetics and Physical Performance
Type
article
Field-Weighted Citation Impact
1.65

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article

Adverse impact of female reproductive signaling on age-dependent neurodegeneration after mild head trauma in Drosophila

James Q. Zheng, Changtian Ye, Kenneth H. Moberg, Ryan Ho
3 citations
eLife
Genetics and Physical Performance
1.65
article

Adverse impact of female reproductive signaling on age-dependent neurodegeneration after mild head trauma in Drosophila

James Q. Zheng, Changtian Ye, Kenneth H. Moberg, Ryan Ho
article en
3 citations

Abstract

Environmental insults, including mild head trauma, significantly increase the risk of neurodegeneration. However, it remains challenging to establish a causative connection between early-life exposure to mild head trauma and late-life emergence of neurodegenerative deficits, nor do we know how sex and age compound the outcome. Using a Drosophila model, we demonstrate that exposure to mild head trauma causes neurodegenerative conditions that emerge late in life and disproportionately affect females. Increasing age-at-injury further exacerbates this effect in a sexually dimorphic manner. We further identify sex peptide signaling as a key factor in female susceptibility to post-injury brain deficits. RNA sequencing highlights a reduction in innate immune defense transcripts specifically in mated females during late life. Our findings establish a causal relationship between early head trauma and late-life neurodegeneration, emphasizing sex differences in injury response and the impact of age-at-injury. Finally, our findings reveal that reproductive signaling adversely impacts female response to mild head insults and elevates vulnerability to late-life neurodegeneration.

eLifeVol. 13
Emory University (US), Institute for Neurodegenerative Disorders (US)
National Institutes of Health
Openalex Percentile: Top 15%
Genetics and Physical Performance
1.65
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