Heightened infiltration of immune effector cell types in the hippocampal regions in the APP/PS1 mouse model of Alzheimer’s disease.

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Presentation Time: 03:15 PM - 04:30 PM
Poster Board Number: B556
Abstract ID: 4276

Presenting Author:
Mark A Maynes , PhD Student at Mayo Clin. Grad. Sch. of Biomed. Sci., Mayo Clin., Minnesota

Abstract:

Alzheimer's disease (AD) is among the most common neurodegenerative diseases in which a role for immune cells in its etiology is only beginning to be realized. AD has two molecular pathological hallmarks: the presence of amyloid beta (Aβ) plaques and tau tangles within neuronal cells. The amyloid plaques can be modeled in mice by inserting transgenes that enhance human Aβ to create plaques inside the mouse brain. Amyloid precursor protein (Mo/HuAPP695swe) and a mutant human presenilin 1 (PS1-dE9) are two transgenes inserted into C57BL/6 mice that results in Aβ plaques in the hippocampus and cortex. This mouse is known as the APP/PS1 mouse. Immune cell infiltration into the brain is associated with aged APP/PS1 mice.  However, comprehensive immune profiling has not been performed in this model to outline immune cell effectors potentially involved in neuropathology. Therefore, we employed spectral flow cytometry to investigate the immune cell profile in 24-month-old APP/PS1 mice compared to an age matched control. There are increased numbers of CD8 T, γδ T, and NK cells expressing perforin and other activation related surface markers. Using small animal MRI imaging, we also observed enlarged ventricles mice indicative of brain atrophy in APP/PS1 mice when compared to wildtype age matched control. These results provide insight into the regional immune cell infiltration of the brain, setting the stage for further analysis of immune mechanisms of neuropathology in experimental AD.