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Senolytic therapy preserves blood-brain barrier integrity and promotes microglia homeostasis in a tauopathy model

Minmin Yao, Zhiliang Wei, Jonathan Scharff Nielsen, Yuxiao Ouyang, Aaron Kakazu, Haitong Wang, Lida Du, Ruoxuan Li, Tiffany Chu, Susanna Scafidi, Hanzhang Lu, Manisha Aggarwal, Wenzhen Duan

Neurobiology of Disease · 2024 · ▲ 28 citations

Abstract

Cellular senescence(definition), characterized by expressing the cell cycle inhibitory proteins, is evident in driving age-related diseases. Senescent cells play a crucial role in the initiation and progression of tau-mediated pathology, suggesting that targeting cell senescence offers a therapeutic potential for treating tauopathy associated diseases. This study focuses on identifying non-invasive biomarkers and validating their responses to a well-characterized senolytic therapy combining dasatinib and quercetin (D + Q), in a widely used tauopathy mouse model, PS19. We employed human-translatable MRI measures, including water extraction with phase-contrast arterial spin tagging (WEPCAST) MRI, T2 relaxation under spin tagging (TRUST), longitudinally assessed brain physiology and high-resolution structural MRI evaluated the brain regional volumes in PS19 mice. Our data reveal increased BBB permeability, decreased oxygen extraction fraction, and brain atrophy in 9-month-old PS19 mice compared to their littermate controls. (D + Q) treatment effectively preserves BBB integrity, rescues cerebral oxygen hypometabolism, attenuates brain atrophy, and alleviates tau hyperphosphorylation in PS19 mice. Mechanistically, D + Q treatment induces a shift of microglia from a disease-associated to a homeostatic state, reducing a senescence-like microglial phenotype marked by increased p16/Ink4a. D + Q-treated PS19 mice exhibit enhanced cue-associated cognitive performance in the tracing fear conditioning test compared to the vehicle-treated littermates, implying improved cognitive function by D + Q treatment. Our results pave the way for application of senolytic treatment as well as these noninvasive MRI biomarkers in clinical trials in tauopathy associated neurological disorders. • Senolytic therapy preserves BBB integrity in PS19 mice. • Senolytic therapy reduces brain atrophy and mitigates tauopathy in PS19 mice. • Senolytic therapy enhances cognitive performance in PS19 mice. • Senolytic therapy shows promising in tauopathy-associated disorders. • MRI measures are promising to evaluate efficacy in tauopathy-associated disorders.

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Provenance

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OpenAlex
DOI
10.1016/j.nbd.2024.106711
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2026-06-15 MST

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APA
Yao, M., Wei, Z., Nielsen, J.S., Ouyang, Y., Kakazu, A., Wang, H., Du, L., Li, R., Chu, T., Scafidi, S., Lu, H., Aggarwal, M., &amp; Duan, W. (2024). Senolytic therapy preserves blood-brain barrier integrity and promotes microglia homeostasis in a tauopathy model. <em>Neurobiology of Disease</em>. https://doi.org/10.1016/j.nbd.2024.106711
Vancouver
Yao M, Wei Z, Nielsen JS, Ouyang Y, Kakazu A, Wang H, et al. Senolytic therapy preserves blood-brain barrier integrity and promotes microglia homeostasis in a tauopathy model. Neurobiology of Disease. 2024. doi:10.1016/j.nbd.2024.106711.
BibTeX
@article{minmin2024Senoly, title = {Senolytic therapy preserves blood-brain barrier integrity and promotes microglia homeostasis in a tauopathy model}, author = {Minmin Yao and Zhiliang Wei and Jonathan Scharff Nielsen and Yuxiao Ouyang and Aaron Kakazu and Haitong Wang and Lida Du and Ruoxuan Li and Tiffany Chu and Susanna Scafidi and Hanzhang Lu and Manisha Aggarwal and Wenzhen Duan}, journal = {Neurobiology of Disease}, year = {2024}, doi = {10.1016/j.nbd.2024.106711}, }

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