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      Paraoxonase-1 and -3 Protein Expression in the Brain of the Tg2576 Mouse Model of Alzheimer’s Disease

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          Abstract

          Background: Brain oxidative lipid damage and inflammation are common in neurodegenerative diseases such as Alzheimer’s disease (AD). Paraoxonase-1 and -3 (PON1 and PON3) protein expression was demonstrated in tissue with no PON1 or PON3 gene expression. In the present study, we examine differences in PON1 and PON3 protein expression in the brain of a mouse model of AD. Methods: we used peroxidase- and fluorescence-based immunohistochemistry in five brain regions (olfactory bulb, forebrain, posterior midbrain, hindbrain and cerebellum) of transgenic (Tg2576) mice with the Swedish mutation (KM670/671NL) responsible for a familial form of AD and corresponding wild-type mice. Results: We found intense PON1 and PON3-positive staining in star-shaped cells surrounding Aβ plaques in all the studied Tg2576 mouse-brain regions. Although we could not colocalize PON1 and PON3 with astrocytes (star-shaped cells in the brain), we found some PON3 colocalization with microglia. Conclusions: These results suggest that (1) PON1 and PON3 cross the blood–brain barrier in discoidal high-density lipoproteins (HDLs) and are transferred to specific brain-cell types; and (2) PON1 and PON3 play an important role in preventing oxidative stress and lipid peroxidation in particular brain-cell types (likely to be glial cells) in AD pathology and potentially in other neurodegenerative diseases as well.

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          Most cited references54

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          Single-cell transcriptomic analysis of Alzheimer’s disease

          Alzheimer's disease is a pervasive neurodegenerative disorder, the molecular complexity of which remains poorly understood. Here, we analysed 80,660 single-nucleus transcriptomes from the prefrontal cortex of 48 individuals with varying degrees of Alzheimer's disease pathology. Across six major brain cell types, we identified transcriptionally distinct subpopulations, including those associated with pathology and characterized by regulators of myelination, inflammation, and neuron survival. The strongest disease-associated changes appeared early in pathological progression and were highly cell-type specific, whereas genes upregulated at late stages were common across cell types and primarily involved in the global stress response. Notably, we found that female cells were overrepresented in disease-associated subpopulations, and that transcriptional responses were substantially different between sexes in several cell types, including oligodendrocytes. Overall, myelination-related processes were recurrently perturbed in multiple cell types, suggesting that myelination has a key role in Alzheimer's disease pathophysiology. Our single-cell transcriptomic resource provides a blueprint for interrogating the molecular and cellular basis of Alzheimer's disease.
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            Microglia and macrophages in brain homeostasis and disease

            Microglia and non-parenchymal macrophages in the brain are mononuclear phagocytes that are increasingly recognized to be essential players in the development, homeostasis and diseases of the central nervous system. With the availability of new genetic, molecular and pharmacological tools, considerable advances have been made towards our understanding of the embryonic origins, developmental programmes and functions of these cells. These exciting discoveries, some of which are still controversial, also raise many new questions, which makes brain macrophage biology a fast-growing field at the intersection of neuroscience and immunology. Here, we review the current knowledge of how and where brain macrophages are generated, with a focus on parenchymal microglia. We also discuss their normal functions during development and homeostasis, the disturbance of which may lead to various neurodegenerative and neuropsychiatric diseases.
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              Correlative memory deficits, Abeta elevation, and amyloid plaques in transgenic mice.

              Transgenic mice overexpressing the 695-amino acid isoform of human Alzheimer beta-amyloid (Abeta) precursor protein containing a Lys670 --> Asn, Met671 --> Leu mutation had normal learning and memory in spatial reference and alternation tasks at 3 months of age but showed impairment by 9 to 10 months of age. A fivefold increase in Abeta(1-40) and a 14-fold increase in Abeta(1-42/43) accompanied the appearance of these behavioral deficits. Numerous Abeta plaques that stained with Congo red dye were present in cortical and limbic structures of mice with elevated amounts of Abeta. The correlative appearance of behavioral, biochemical, and pathological abnormalities reminiscent of Alzheimer's disease in these transgenic mice suggests new opportunities for exploring the pathophysiology and neurobiology of this disease.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Antioxidants (Basel)
                Antioxidants (Basel)
                antioxidants
                Antioxidants
                MDPI
                2076-3921
                24 February 2021
                March 2021
                : 10
                : 3
                : 339
                Affiliations
                [1 ]Department of Psychology and Research Center for Behavioral Assessment (CRAMC), Universitat Rovira i Virgili, 43007 Tarragona, Spain; salazarjg@ 123456ula.ve (J.G.S.); ingrid.reverte@ 123456uniroma1.it (I.R.)
                [2 ]Research in Neurobehavior and Health (NEUROLAB), Universitat Rovira i Virgili, 43201 Reus, Spain
                [3 ]Departamento de Toxicología y Farmacología, Facultad de Farmacia y Bioanálisis, Universidad de Los Andes, Mérida 5101, Venezuela
                [4 ]Unitat de Recerca Biomèdica, Hospital Universitari de Sant Joan, Institut d’Investigació Sanitària Pere Virgili, Universitat Rovira i Virgili, 43201 Reus, Spain; jmarsi@ 123456uw.edu (J.M.); jjoven@ 123456grupsagessa.com (J.J.)
                [5 ]Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, WA 98105, USA
                [6 ]Department of Physiology and Pharmacology, Sapienza University of Rome, 00185 Rome, Italy
                [7 ]Santa Lucia Foundation (IRCCS Fondazione Santa Lucia), 00179 Rome, Italy
                [8 ]Miami Platja, 43892 Tarragona, Spain; bharti.mackness@ 123456gmail.com (B.M.); mike.mackness@ 123456gmail.com (M.M.)
                Author notes
                [* ]Correspondence: jcamps@ 123456grupsagessa.com (J.C.); mariateresa.colomina@ 123456urv.cat (M.T.C.); Tel.: +34-977-558153 (M.T.C.)
                [†]

                These authors contributed equally to this work.

                Author information
                https://orcid.org/0000-0002-3061-6266
                https://orcid.org/0000-0003-2749-4541
                https://orcid.org/0000-0002-5619-4874
                Article
                antioxidants-10-00339
                10.3390/antiox10030339
                7996151
                33668379
                d20db97a-84a9-4724-8b2b-de2de53eaff3
                © 2021 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 30 November 2020
                : 20 February 2021
                Categories
                Article

                paraoxonases,oxidative stress,alzheimer’s disease,brain,tg2576 mice,astrocytes,hippocampus,amyloid-β,microglia,neurons

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