In this study, the distinct patterns of glial response and neurodegeneration within the CA1, CA3, and dentate gyrus (DG) regions of the hippocampus were examined in 5XFAD mice at 6 and 12 months of age. The primary feature of this transgenic mouse model is the rapid onset of amyloid pathology. We employed quantitative assessments via immunohistochemistry, incorporating double staining techniques, followed by observation with light microscopy and subsequent digital analysis of microscopic images. We identified significantly increased A beta deposition in these three hippocampal regions at 6 and 12 months of transgenic mice. Moreover, the CA1 and CA3 regions showed higher vulnerability, with signs of reactive astrogliosis such as increased astrocyte density and elevated GFAP expression. Additionally, we observed a significant rise in microglia density, along with elevated inflammatory markers (TNF alpha) in these hippocampal regions. These findings highlight a non-uniform glial and neuronal response to A beta plaque deposition within the hippocampal regions of 5xFAD mice, potentially contributing to the neurodegenerative and memory deficit characteristics of Alzheimer's disease in this model.
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Alzheimer A., 1910, Beitrge zur Kenntnis der Pathologischen Neuroglia und ihrer Beziehungen zu den Abbauvorgngen im Nervengewebe. G. Fischer
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Rush Univ, Med Ctr, Rush Alzheimers Dis Ctr, Chicago, IL 60612 USARush Univ, Med Ctr, Rush Alzheimers Dis Ctr, Chicago, IL 60612 USA
Buchman, A. S.
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Boyle, P. A.
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Rush Univ, Med Ctr, Rush Alzheimers Dis Ctr, Chicago, IL 60612 USA
Rush Univ, Med Ctr, Dept Family Med, Chicago, IL 60612 USARush Univ, Med Ctr, Rush Alzheimers Dis Ctr, Chicago, IL 60612 USA
Boyle, P. A.
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Yu, L.
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Yu, L.
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Shah, R. C.
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Rush Univ, Med Ctr, Rush Alzheimers Dis Ctr, Chicago, IL 60612 USA
Rush Univ, Med Ctr, Dept Family Med, Chicago, IL 60612 USARush Univ, Med Ctr, Rush Alzheimers Dis Ctr, Chicago, IL 60612 USA
Shah, R. C.
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Wilson, R. S.
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Wilson, R. S.
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Bennett, D. A.
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Rush Univ, Med Ctr, Rush Alzheimers Dis Ctr, Chicago, IL 60612 USARush Univ, Med Ctr, Rush Alzheimers Dis Ctr, Chicago, IL 60612 USA
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Univ Calif Los Angeles, Dept Neurobiol, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, Brain Res Inst, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Dept Neurobiol, Los Angeles, CA 90095 USA
Burda, Joshua E.
;
Sofroniew, Michael V.
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Univ Calif Los Angeles, Dept Neurobiol, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, Brain Res Inst, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Dept Neurobiol, Los Angeles, CA 90095 USA
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Rush Univ, Med Ctr, Rush Alzheimers Dis Ctr, Chicago, IL 60612 USARush Univ, Med Ctr, Rush Alzheimers Dis Ctr, Chicago, IL 60612 USA
Buchman, A. S.
;
Boyle, P. A.
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Rush Univ, Med Ctr, Rush Alzheimers Dis Ctr, Chicago, IL 60612 USA
Rush Univ, Med Ctr, Dept Family Med, Chicago, IL 60612 USARush Univ, Med Ctr, Rush Alzheimers Dis Ctr, Chicago, IL 60612 USA
Boyle, P. A.
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Yu, L.
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Rush Univ, Med Ctr, Rush Alzheimers Dis Ctr, Chicago, IL 60612 USARush Univ, Med Ctr, Rush Alzheimers Dis Ctr, Chicago, IL 60612 USA
Yu, L.
;
Shah, R. C.
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Rush Univ, Med Ctr, Rush Alzheimers Dis Ctr, Chicago, IL 60612 USA
Rush Univ, Med Ctr, Dept Family Med, Chicago, IL 60612 USARush Univ, Med Ctr, Rush Alzheimers Dis Ctr, Chicago, IL 60612 USA
Shah, R. C.
;
Wilson, R. S.
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Rush Univ, Med Ctr, Rush Alzheimers Dis Ctr, Chicago, IL 60612 USARush Univ, Med Ctr, Rush Alzheimers Dis Ctr, Chicago, IL 60612 USA
Wilson, R. S.
;
Bennett, D. A.
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Rush Univ, Med Ctr, Rush Alzheimers Dis Ctr, Chicago, IL 60612 USARush Univ, Med Ctr, Rush Alzheimers Dis Ctr, Chicago, IL 60612 USA
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Univ Calif Los Angeles, Dept Neurobiol, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, Brain Res Inst, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Dept Neurobiol, Los Angeles, CA 90095 USA
Burda, Joshua E.
;
Sofroniew, Michael V.
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Univ Calif Los Angeles, Dept Neurobiol, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, Brain Res Inst, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Dept Neurobiol, Los Angeles, CA 90095 USA