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Engulfment of tangle-bearing neurons by microglia in a living tauopathy model

https://repo.qst.go.jp/records/67065
https://repo.qst.go.jp/records/67065
66b7430d-fd1e-4963-b7cf-fd7ceda15f20
Item type 会議発表用資料 / Presentation(1)
公開日 2018-12-27
タイトル
タイトル Engulfment of tangle-bearing neurons by microglia in a living tauopathy model
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_c94f
資源タイプ conference object
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 田桑, 弘之

× 田桑, 弘之

WEKO 659262

田桑, 弘之

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田桑 弘之

× 田桑 弘之

WEKO 659263

en 田桑 弘之

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内容記述タイプ Abstract
内容記述 Accumulation of intracellular neurofibrillary tangles (NFTs) consisting of microtubule-associated protein tau is a major hallmark of Alzheimer’s disease ad related neurodegenerative diseases referred to as tauopathies, while mechanisms underlying tau-mediated neurodegeneration remain unclear. To elucidate molecular and cellular processes mediating the death of neurons bearing NFTs, we conducted in vivo multimodal imaging studies, consisting of PET, MRI and two-photon microscopy of an inducible transgenic mouse model expressing human 0N4R tau with the P301L mutation, termed rTg4510 mice. Longitudinal PET/MRI studies revealed age-dependent pathological tau accumulation, microglial activation and volume reduction in the cortex and hippocampus. We observed plateaued tau pathology, as there was no significant difference in tau PET signals between rTg4510 mice at 7 and 12-14 months of age. Correspondingly, in vivo two-photon microscopy demonstrated a plateaued total amount of tau inclusions after 7 months of age. This was attributed to equilibrium between emergence of new tau inclusions and disappearance of tangle-bearing neurons, and the rates of these two events were significantly reduced by doxycycline-induced suppression of transgenic human P301L tau. Most interestingly, daily two-photon microscopic observations of individual mCherry-expressing neurons and GFP-expressing microglia illustrated engulfment of tangle-burdened neurons by hypertrophic cell bodies or processes of microglia, followed by elimination of these neurons. These data suggest an essential role of phagocytic microglia in tau-induced neuronal death. Further studies are ongoing to search for molecular signals triggering phagocytic microglial activation.
会議概要(会議名, 開催地, 会期, 主催者等)
内容記述タイプ Other
内容記述 北米神経科学会
発表年月日
日付 2018-11-04
日付タイプ Issued
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