Blood-Brain Barrier Dysfunction in Normal Aging and Neurodegeneration: Mechanisms, Impact, and Treatments

Author:

Andjelkovic Anuska V.12,Situ Muyu3ORCID,Citalan-Madrid Ali Francisco1,Stamatovic Svetlana M.1ORCID,Xiang Jianming2,Keep Richard F.24ORCID

Affiliation:

1. Department of Pathology (A.V.A., A.F.C.-M., S.M.S.), University of Michigan Medical School, Ann Arbor.

2. Department of Neurosurgery (A.V.A., J.X., R.F.K.), University of Michigan Medical School, Ann Arbor.

3. Neuroscience Graduate Program (M.S.), University of Michigan Medical School, Ann Arbor.

4. Department of Molecular and Integrative Physiology (R.F.K.), University of Michigan Medical School, Ann Arbor.

Abstract

Cerebral endothelial cells and their linking tight junctions form a unique, dynamic and multi-functional interface, the blood-brain barrier (BBB). The endothelium is regulated by perivascular cells and components forming the neurovascular unit. This review examines BBB and neurovascular unit changes in normal aging and in neurodegenerative disorders, particularly focusing on Alzheimer disease, cerebral amyloid angiopathy and vascular dementia. Increasing evidence indicates BBB dysfunction contributes to neurodegeneration. Mechanisms underlying BBB dysfunction are outlined (endothelium and neurovascular unit mediated) as is the BBB as a therapeutic target including increasing the uptake of systemically delivered therapeutics across the BBB, enhancing clearance of potential neurotoxic compounds via the BBB, and preventing BBB dysfunction. Finally, a need for novel biomarkers of BBB dysfunction is addressed.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Advanced and Specialized Nursing,Cardiology and Cardiovascular Medicine,Neurology (clinical)

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