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Kitty Murphy

@kittybmurphy.bsky.social
486 followers 571 following 28 posts

Postdoc at Globe Institute, University of Copenhagen 🇩🇰 she/her Interested in the phenotypic effects of archaic DNA present in modern human genomes 🧬

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Kitty Murphy @kittybmurphy.bsky.social · 02/07/2026
@mexpositoalonso.bsky.social has officially converted me into a plant person 🌱 #SMBE2026
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Kitty Murphy @kittybmurphy.bsky.social · 28/05/2025
Lastly, we were excited to find that regions with increased chromatin accessibility in APOE2 microglia were enriched for vitamin D receptor binding, suggesting vitamin D signalling as a potential protective mechanism and therapeutic avenue. 6/n
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Kitty Murphy @kittybmurphy.bsky.social · 28/05/2025
Comparison with independent studies showed that APOE2 microglia were enriched for plaque-phagocytosing genes, prompting us to test their phagocytic activity. Using E. coli and myelin, we found that they were indeed more phagocytic than APOE4 microglia. 5/n
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Kitty Murphy @kittybmurphy.bsky.social · 28/05/2025
Genes downregulated in APOE4-expressing microglia were enriched in putatively protective microglial states, suggesting a failure to transition into these states. Additionally, cytokine expression was elevated, consistent with previous findings in mouse microglia expressing APOE4. 4/n
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Kitty Murphy @kittybmurphy.bsky.social · 28/05/2025
We observed consistent differences in gene expression and chromatin accessibility. For example, the cellular migration-related gene CHCHD2 showed higher expression and increased chromatin accessibility near its transcription start site in APOE2 microglia. 3/n
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Kitty Murphy @kittybmurphy.bsky.social · 28/05/2025
As anticipated, the most pronounced differences were observed between APOE4 (risk-increasing in some populations) and APOE2 (protective). Expression changes were partly driven by loss of function, but only genes downregulated in APOE4 and KO microglia were enriched for AD risk variants. 2/n
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Kitty Murphy @kittybmurphy.bsky.social · 28/05/2025
Excited to share that a chapter of my PhD has just been published in Nature Communications! We profiled the transcriptomic and chromatin landscapes of microglia expressing the different APOE variants, which were xenografted into the brains of an Alzheimer's disease (AD) mouse model 🧠🧬 1/n
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Kitty Murphy @kittybmurphy.bsky.social · 15/05/2025
And just like that, 5 years in the Marzi lab @sj-marzi.bsky.social have come to an end. Couldn’t have asked for a better team ✨ Super excited to say, I’m switching fields and will be working with ancient human genomes in the Skov lab @lauritsskov.bsky.social in Copenhagen 🇩🇰
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