Microneedle Delivery of Small Extracellular Vesicles From Young Blood to Treat Endothelial Senescence

Доставка микроиглами малых внеклеточных везикул из «молодой» крови для лечения старения эндотелия
Zhenhua Li, Malcolm Xing, Dashuai Zhu, Shiqi Hu, Shuo Liu, Ke Cheng
2025-08-05

endothelial senescencemicroneedle transdermal deliverysingle-cell RNA sequencingsmall extracellular vesicles (sEVs)umbilical cord plasma (young sEVs)
Circulating extracellular vesicles (EVs) play a crucial role in mediating communication between different cell populations and organs, significantly influencing inflammation and vascular diseases. To evaluate the role of EVs in regulating senescence, small EVs isolated from umbilical cord plasma (young sEVs, Y-sEVs) are compared with those from the plasma of elderly individuals (old sEVs, O-sEVs, >70 years old) to identify key cargo components. To investigate their effects on senescence, Y-sEVs or O-sEVs are administered to aged mice using transdermal microneedle patches, enabling sustained EV release into the circulation. Doxorubicin is administered to induce enhanced endothelial senescence in aged mice (22-24 months old). Single-cell RNA sequencing revealed that Y-sEV treatment downregulated senescence-related genes in endothelial cells decreased the proportion of activated fibroblasts in the heart, and reduced disease-associated microglia in the brain. Delivery of Y-sEVs via microneedle patches preserved endothelial cell function, and mitigated inflammation and senescence, whereas O-sEVs exacerbated endothelial dysfunction.
1
Doxorubicin-induced enhanced endothelial senescence in aged mice was used as a model to demonstrate that Y-sEVs counteract, whereas O-sEVs worsen, endothelial senescence and inflammation.
2
Small EVs from elderly plasma (O-sEVs, >70 years) exacerbate endothelial dysfunction, in contrast to the protective effects of Y-sEVs.
3
Small extracellular vesicles from umbilical cord plasma (Y-sEVs) delivered via transdermal microneedle patches downregulate senescence-related genes in endothelial cells of aged mice.
4
Transdermal microneedle delivery enables sustained systemic release of Y-sEVs and preserves endothelial cell function while mitigating inflammation and senescence in aged mice.
5
Y-sEV treatment decreases the proportion of activated fibroblasts in the heart and reduces disease-associated microglia in the brain, as shown by single-cell RNA sequencing.

Small extracellular vesicles (sEVs) from human umbilical cord plasma delivered via transdermal microneedle patches to aged mice

Effects of young versus old plasma-derived sEVs on endothelial senescence, endothelial cell function, inflammation, and related cellular states (activated fibroblasts, disease-associated microglia) in aged/doxorubicin-treated mice

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2025-08-05
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Zhenhua Li
Malcolm Xing
Dashuai Zhu
Shiqi Hu
Shuo Liu
Ke Cheng
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