Cranial irradiation significantly reduces beta amyloid plaques in the brain and improves cognition in a murine model of Alzheimer’s Disease (AD)

Abstract Background and purpose To investigate if cranial X-irradiation reduces amyloid-β (Aβ) plaques and influences cognitive function in a transgenic mouse model of AD. Methods and materials B6.Cg-Tg (APPswePSEN1dE9)85Dbo/J AD-prone mice were given cranial X-irradiation. The number of Aβ plaques,...

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Veröffentlicht in:Radiotherapy and oncology 2016-01, Vol.118 (1), p.43-51
Hauptverfasser: Marples, Brian, McGee, Mackenzie, Callan, Sean, Bowen, Scott E, Thibodeau, Bryan J, Michael, Daniel B, Wilson, George D, Maddens, Michael E, Fontanesi, James, Martinez, Alvaro A
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Sprache:eng
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Zusammenfassung:Abstract Background and purpose To investigate if cranial X-irradiation reduces amyloid-β (Aβ) plaques and influences cognitive function in a transgenic mouse model of AD. Methods and materials B6.Cg-Tg (APPswePSEN1dE9)85Dbo/J AD-prone mice were given cranial X-irradiation. The number of Aβ plaques, along with expression of AD specific genes (84 genes: Mouse Alzheimer’s Disease RT2 Profiler™), radiation-associated cytokines (Milliplex® MAP Mouse Cytokine Chemokine Immunoassay) and immunohistochemistry (IL10, IL-1β, Iba1 CD45) was assessed. Behavioral testing was performed to relate changes in Aβ burden to cognitive function using a Morris water-maze task. Results Single X-ray doses reduced the number ( p = 0.002) and size ( p = 0.01) of Aβ plaques. Low-dose fractionation produced greater 50.6% (1 Gy × 10), 72% (2 Gy × 5) and 78% (2 Gy × 10) reductions. Irradiation was associated with gene (Pkp4, 1.5-fold, p = 0.004) and proteomic (MIP-2, 8-fold, p = 0.0024) changes at 24–48 h. Microglia increased at 4 weeks post-irradiation ( p = 0.001). The reduction in Aβ burden (2 Gy × 5) was associated with cognitive improvement ( p = 0.012). Conclusion This is the first report that a clinically relevant course of external beam irradiation (2 Gy × 5) produces a significant reduction in AD-associated amyloid-β plaques with a subsequent improvement in cognitive function. However, longer-term studies are needed to define the precise underlying mechanism and longevity of this response.
ISSN:0167-8140
1879-0887
DOI:10.1016/j.radonc.2015.10.019