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      Pathological changes within the cerebral vasculature in Alzheimer’s disease: New perspectives

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          Abstract

          Cerebrovascular disease underpins vascular dementia (VaD), but structural and functional changes to the cerebral vasculature contribute to disease pathology and cognitive decline in Alzheimer's disease (AD). In this review, we discuss the contribution of cerebral amyloid angiopathy and non‐amyloid small vessel disease in AD, and the accompanying changes to the density, maintenance and remodelling of vessels (including alterations to the composition and function of the cerebrovascular basement membrane). We consider how abnormalities of the constituent cells of the neurovascular unit – particularly of endothelial cells and pericytes – and impairment of the blood‐brain barrier (BBB) impact on the pathogenesis of AD. We also discuss how changes to the cerebral vasculature are likely to impair Aβ clearance – both intra‐periarteriolar drainage (IPAD) and transport of Aβ peptides across the BBB, and how impaired neurovascular coupling and reduced blood flow in relation to metabolic demand increase amyloidogenic processing of APP and the production of Aβ. We review the vasoactive properties of Aβ peptides themselves, and the probable bi‐directional relationship between vascular dysfunction and Aβ accumulation in AD. Lastly, we discuss recent methodological advances in transcriptomics and imaging that have provided novel insights into vascular changes in AD, and recent advances in assessment of the retina that allow in vivo detection of vascular changes in the early stages of AD.

          Abstract

          Structural and functional changes to blood vessels not only underpin disease pathogenesis in vascular dementia but are also major contributors to cognitive decline and disease progression in Alzheimer’s disease. We provide an updated review on the clinical and neuropathological vascular features (SVD, CAA) and underpinning functional changes to blood vessels in relation of disease pathology in Alzheimer’s disease. We also discuss recent methodological advances within the field that have provided novel insights into vascular changes in AD, including transcriptomics, imaging, and retinal assessment providing a window of opportunity for future clinical intervention.

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          The extracellular matrix at a glance.

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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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              Blood–brain barrier breakdown in Alzheimer disease and other neurodegenerative disorders

              The blood-brain barrier (BBB) is a continuous endothelial membrane within brain microvessels that has sealed cell-to-cell contacts and is sheathed by mural vascular cells and perivascular astrocyte end-feet. The BBB protects neurons from factors present in the systemic circulation and maintains the highly regulated CNS internal milieu, which is required for proper synaptic and neuronal functioning. BBB disruption allows influx into the brain of neurotoxic blood-derived debris, cells and microbial pathogens and is associated with inflammatory and immune responses, which can initiate multiple pathways of neurodegeneration. This Review discusses neuroimaging studies in the living human brain and post-mortem tissue as well as biomarker studies demonstrating BBB breakdown in Alzheimer disease, Parkinson disease, Huntington disease, amyotrophic lateral sclerosis, multiple sclerosis, HIV-1-associated dementia and chronic traumatic encephalopathy. The pathogenic mechanisms by which BBB breakdown leads to neuronal injury, synaptic dysfunction, loss of neuronal connectivity and neurodegeneration are described. The importance of a healthy BBB for therapeutic drug delivery and the adverse effects of disease-initiated, pathological BBB breakdown in relation to brain delivery of neuropharmaceuticals are briefly discussed. Finally, future directions, gaps in the field and opportunities to control the course of neurological diseases by targeting the BBB are presented.
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                Author and article information

                Contributors
                Robbie.fisher@bristol.ac.uk
                Seth.Love@bristol.ac.uk
                Journal
                Brain Pathol
                Brain Pathol
                10.1111/(ISSN)1750-3639
                BPA
                Brain Pathology
                John Wiley and Sons Inc. (Hoboken )
                1015-6305
                1750-3639
                14 March 2022
                November 2022
                : 32
                : 6 ( doiID: 10.1111/bpa.v32.6 )
                : e13061
                Affiliations
                [ 1 ] Dementia Research Group University of Bristol Medical School Bristol UK
                Author notes
                [*] [* ] Correspondence

                Robert A. Fisher, Dementia Research Group, Learning and Research, Level 1, Southmead Hospital, Bristol Medical School, University of Bristol, Bristol BS10 5NB, UK.

                Email: Robbie.fisher@ 123456bristol.ac.uk

                Seth Love, Learning and Research, Level 2, Southmead Hospital, Bristol BS10 5NB, UK.

                Email: Seth.Love@ 123456bristol.ac.uk

                Author information
                https://orcid.org/0000-0002-0387-290X
                https://orcid.org/0000-0001-8594-1640
                https://orcid.org/0000-0001-8683-3625
                Article
                BPA13061
                10.1111/bpa.13061
                9616094
                35289012
                3a660220-4fd6-46ae-89de-090c0c1c1e72
                © 2022 The Authors. Brain Pathology published by John Wiley & Sons Ltd on behalf of International Society of Neuropathology

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 11 February 2022
                : 10 December 2021
                : 21 February 2022
                Page count
                Figures: 4, Tables: 2, Pages: 23, Words: 18069
                Funding
                Funded by: Alzheimer’s Research UK , doi 10.13039/501100002283;
                Award ID: ARUK‐SRF‐2019A‐001
                Categories
                Invited Review
                Invited Review
                Custom metadata
                2.0
                November 2022
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.2.0 mode:remove_FC converted:28.10.2022

                Pathology
                alzheimer's disease,blood‐brain barrier,cerebral blood flow,neurovascular coupling,pericyte,vasculature

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