Stroke is the third leading cause of death and the leading cause of serious, long-term disability in the U.S. However, while advances have been made in acute stroke treatment, our understanding of the mechanisms underlying brain self-repair after stroke remains poor. Therefore, the problem of brain repair and stroke rehabilitation is an emerging research priority, with the underlying goal of identifying and improving brain reparative processes. Brain repair reportedly occurs in a close temporal-spatial neurovascular niche of revascularization (angiogenesis) and neuronal repopulation (neurogenesis). We hypothesize that the post-stroke brain stimulates angiogenesis and neurovascular niche formation in part by generating a bioactive fragment of the extracellular matrix (ECM), perlecan. Our hypothesis is based on several key observations including our preliminary data: Stroke results in proteolytic generation of bioactive fragments of perlecan, the most protease-sensitive ECM component studied, and perlecan is required for both angiogenesis and neurogenesis. Our preliminary studies indicate that the C-terminal fragment of perlecan, domain V (DV), a previously identified modifier of angiogenesis, 1) is upregulated in the brain after stroke, 2) enhances brain angiogenesis in vitro and in vivo, 3) increases brain endothelial cell secretion of brain derived neurotrophic factor (BDNF), an important pro-angiogenic, neuroprotective and migration promoting factor in the neurovascular niche, and 4) may exert these effects through the pro-angiogenic (5(1 integrin. Empowered by this new knowledge, we now plan to 1) Determine the role of DV in brain angiogenesis and neurovascular niche formation, 2) Determine the integrin-related signaling pathway by which DV affects brain angiogenesis and neurovascular niche formation, and 3) Determine the importance and therapeutic potential of DV to post-stroke brain repair. Specifically, we plan to demonstrate that DV stimulates brain angiogenesis and neurovascular niche formation via interaction with the (5(1 integrin and subsequent release of BDNF, and demonstrate that DV enhances post-stroke brain repair. The proposed studies are significant in that they investigates differences between brain and nonbrain angiogenesis, seek to establish a novel mechanism of post-stroke brain self-repair for therapeutic exploitation, and suggests a significantly longer therapeutic window than currently employed stroke therapies. Our investigation is innovative because it suggests that ECM fragments generated by brain injury could possess beneficial effects and identifies a novel cause of brain endothelial cell BDNF release. Our long term goal is to develop DV as a human stroke therapy.

Public Health Relevance

Stroke is the third leading cause of death and the leading cause of serious, long-term disability in the U.S. However, while advances have been made in trying to minimize brain injury after stroke, little is known about how to stimulate repair of injured brain tissue. Therefore, we propose to study the potential benefits of a stroke-generated protein fragment in a stroke animal model, with the goal of developing a new type of human stroke therapy.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS065842-06
Application #
8583355
Study Section
Brain Injury and Neurovascular Pathologies Study Section (BINP)
Program Officer
Bosetti, Francesca
Project Start
2010-04-01
Project End
2015-03-31
Budget Start
2013-04-01
Budget End
2014-03-31
Support Year
6
Fiscal Year
2013
Total Cost
$307,205
Indirect Cost
$100,333
Name
University of Kentucky
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
939017877
City
Lexington
State
KY
Country
United States
Zip Code
40506
Jullienne, Amandine; Roberts, Jill M; Pop, Viorela et al. (2014) Juvenile traumatic brain injury induces long-term perivascular matrix changes alongside amyloid-beta accumulation. J Cereb Blood Flow Metab 34:1637-45
Parham, Christi; Auckland, Lisa; Rachwal, Jessica et al. (2014) Perlecan domain V inhibits amyloid-* induced brain endothelial cell toxicity and restores angiogenic function. J Alzheimers Dis 38:415-23
Saini, Maxim G; Bix, Gregory J (2012) Oxygen-glucose deprivation (OGD) and interleukin-1 (IL-1) differentially modulate cathepsin B/L mediated generation of neuroprotective perlecan LG3 by neurons. Brain Res 1438:65-74
Saini, Maxim G; Pinteaux, Emmanuel; Lee, Boyeon et al. (2011) Oxygen-glucose deprivation and interleukin-1ýý trigger the release of perlecan LG3 by cells of neurovascular unit. J Neurochem 119:760-71
Lee, Boyeon; Clarke, Douglas; Al Ahmad, Abraham et al. (2011) Perlecan domain V is neuroprotective and proangiogenic following ischemic stroke in rodents. J Clin Invest 121:3005-23