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In vivo uptake of β-amyloid by non-plaque associated microglia

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In vivo uptake of β-amyloid by non-plaque associated microglia. / Hawkes, Cheryl A.; Deng, LeHua H.; Fenili, Daniela et al.
In: Current Alzheimer Research, Vol. 9, No. 8, 26.10.2012, p. 890-901.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Hawkes, CA, Deng, LH, Fenili, D, Nitz, M & McLaurin, JA 2012, 'In vivo uptake of β-amyloid by non-plaque associated microglia', Current Alzheimer Research, vol. 9, no. 8, pp. 890-901. https://doi.org/10.2174/156720512803251084

APA

Hawkes, C. A., Deng, L. H., Fenili, D., Nitz, M., & McLaurin, J. A. (2012). In vivo uptake of β-amyloid by non-plaque associated microglia. Current Alzheimer Research, 9(8), 890-901. https://doi.org/10.2174/156720512803251084

Vancouver

Hawkes CA, Deng LH, Fenili D, Nitz M, McLaurin JA. In vivo uptake of β-amyloid by non-plaque associated microglia. Current Alzheimer Research. 2012 Oct 26;9(8):890-901. doi: 10.2174/156720512803251084

Author

Hawkes, Cheryl A. ; Deng, LeHua H. ; Fenili, Daniela et al. / In vivo uptake of β-amyloid by non-plaque associated microglia. In: Current Alzheimer Research. 2012 ; Vol. 9, No. 8. pp. 890-901.

Bibtex

@article{794e8b86eeee4d69a62d95562ef79ef5,
title = "In vivo uptake of β-amyloid by non-plaque associated microglia",
abstract = "The role of microglia in β-amyloid (Aβ) deposition or clearance in the Alzheimer's disease (AD) brain remains unclear. Previous in vivo studies have focused primarily on the association of microglia with Aβ-positive parenchymal plaques, but have given little consideration to the possible interaction between Aβ and non-plaque associated microglia. Further, it is not known if microglia play a direct role in mediating Aβ uptake following anti-aggregant treatment. We report here the identification of Aβ-positive processes throughout the cortex and hippocampus of TgCRND8 mice expressing the human Swedish (KM670/671NL) and Indiana (V717F) amyloid precursor protein mutations, which localized to ionized calcium binding protein-1-positive resident microglia that were not associated with extracellular plaques. Oral administration of 1-deoxy-1-fluoro-scyllo-inositol, a scyllo-inositol analogue, to TgCRND8 mice improved spatial memory impairments and suppressed amyloid pathology in a dose-dependent manner. Further, treatment with 1-deoxy-1- fluoro-scyllo-inositol significantly increased hippocampal intra-microglial Aβ levels without stimulating microglial proliferation or peripheral macrophage recruitment. These results reveal a novel, beneficial role for non-plaque associated microglia in the regulation of cerebral Aβ levels in a mouse model of AD.",
keywords = "Alzheimer's disease, Anti-aggregant, Transgenic mouse model",
author = "Hawkes, {Cheryl A.} and Deng, {LeHua H.} and Daniela Fenili and Mark Nitz and McLaurin, {JoAnne A.}",
year = "2012",
month = oct,
day = "26",
doi = "10.2174/156720512803251084",
language = "English",
volume = "9",
pages = "890--901",
journal = "Current Alzheimer Research",
issn = "1567-2050",
publisher = "Bentham Science Publishers B.V.",
number = "8",

}

RIS

TY - JOUR

T1 - In vivo uptake of β-amyloid by non-plaque associated microglia

AU - Hawkes, Cheryl A.

AU - Deng, LeHua H.

AU - Fenili, Daniela

AU - Nitz, Mark

AU - McLaurin, JoAnne A.

PY - 2012/10/26

Y1 - 2012/10/26

N2 - The role of microglia in β-amyloid (Aβ) deposition or clearance in the Alzheimer's disease (AD) brain remains unclear. Previous in vivo studies have focused primarily on the association of microglia with Aβ-positive parenchymal plaques, but have given little consideration to the possible interaction between Aβ and non-plaque associated microglia. Further, it is not known if microglia play a direct role in mediating Aβ uptake following anti-aggregant treatment. We report here the identification of Aβ-positive processes throughout the cortex and hippocampus of TgCRND8 mice expressing the human Swedish (KM670/671NL) and Indiana (V717F) amyloid precursor protein mutations, which localized to ionized calcium binding protein-1-positive resident microglia that were not associated with extracellular plaques. Oral administration of 1-deoxy-1-fluoro-scyllo-inositol, a scyllo-inositol analogue, to TgCRND8 mice improved spatial memory impairments and suppressed amyloid pathology in a dose-dependent manner. Further, treatment with 1-deoxy-1- fluoro-scyllo-inositol significantly increased hippocampal intra-microglial Aβ levels without stimulating microglial proliferation or peripheral macrophage recruitment. These results reveal a novel, beneficial role for non-plaque associated microglia in the regulation of cerebral Aβ levels in a mouse model of AD.

AB - The role of microglia in β-amyloid (Aβ) deposition or clearance in the Alzheimer's disease (AD) brain remains unclear. Previous in vivo studies have focused primarily on the association of microglia with Aβ-positive parenchymal plaques, but have given little consideration to the possible interaction between Aβ and non-plaque associated microglia. Further, it is not known if microglia play a direct role in mediating Aβ uptake following anti-aggregant treatment. We report here the identification of Aβ-positive processes throughout the cortex and hippocampus of TgCRND8 mice expressing the human Swedish (KM670/671NL) and Indiana (V717F) amyloid precursor protein mutations, which localized to ionized calcium binding protein-1-positive resident microglia that were not associated with extracellular plaques. Oral administration of 1-deoxy-1-fluoro-scyllo-inositol, a scyllo-inositol analogue, to TgCRND8 mice improved spatial memory impairments and suppressed amyloid pathology in a dose-dependent manner. Further, treatment with 1-deoxy-1- fluoro-scyllo-inositol significantly increased hippocampal intra-microglial Aβ levels without stimulating microglial proliferation or peripheral macrophage recruitment. These results reveal a novel, beneficial role for non-plaque associated microglia in the regulation of cerebral Aβ levels in a mouse model of AD.

KW - Alzheimer's disease

KW - Anti-aggregant

KW - Transgenic mouse model

U2 - 10.2174/156720512803251084

DO - 10.2174/156720512803251084

M3 - Journal article

C2 - 22272621

AN - SCOPUS:84864318278

VL - 9

SP - 890

EP - 901

JO - Current Alzheimer Research

JF - Current Alzheimer Research

SN - 1567-2050

IS - 8

ER -