Focal microvascular lesions ? such as microinfarcts and microhemorrhages ? are frequently observed in the brains of older individuals and are strongly associated with cognitive impairment and dementia. Yet, the underlying pathophysiological mechanisms and structural and functional consequences of these lesions are poorly understood. This proposal aims to unravel the mechanisms underlying microvascular lesion formation and their impact on local and remote vascular and neuronal networks, in the context of cerebral amyloid angiopathy (CAA). CAA is one of the most common age-related cerebral small vessel diseases, characterized by the accumulation of amyloid ? in small cortical arterioles. It has been suggested that vascular amyloid deposition involves a self-reinforcing cycle of vascular smooth muscle cell degeneration and impaired perivascular clearance of solutes (including amyloid) from the brain, which eventually results in the formation of microinfarcts and microhemorrhages. Although CAA has traditionally been considered a local disease resulting in focal lesions from individually affected cortical vessels, recent preliminary observations suggest profound alterations in surrounding vascular and neuronal networks, with more remote brain tissue injury as a result. The proposed research will address these network-wide effects of local vascular amyloid accumulation, by combining advanced neuroimaging and histopathology techniques in ex vivo human brains with cutting- edge optical imaging tools in living mice. The proposal builds on the applicants? international leadership in CAA, their strong background in post-mortem MRI and state-of-the-art histopathology techniques, and pioneering work in two-photon microscopy of mouse models with CAA. Combined with the world-class resources and international collaborations with experts in the field to perform advanced image processing, the proposed set of experiments will likely yield much needed answers regarding the mechanisms involved in cerebral small vessel disease. Novel insights resulting from this project may also yield promising new targets to prevent vascular cognitive impairment and dementia in the elderly.

Public Health Relevance

The proposed research aims to unravel the mechanisms responsible for microvascular lesion formation in age- related cerebral small vessel disease and their impact on brain structural and functional vascular and neuronal networks. The multi-modal approach combines advanced neuroimaging techniques and neuropathological examination in human brain tissue with state-of-the-art optical tools to monitor the local and remote effects of microvascular lesions on the brain in real-time in living mice. The results will improve our understanding of the mechanisms involved in small vessel disease and may also yield promising new targets to prevent vascular cognitive impairment and dementia.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Multi-Year Funded Research Project Grant (RF1)
Project #
3RF1NS110054-01S1
Application #
10241673
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Corriveau, Roderick A
Project Start
2018-09-30
Project End
2021-05-31
Budget Start
2020-09-01
Budget End
2021-05-31
Support Year
1
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
073130411
City
Boston
State
MA
Country
United States
Zip Code
02114