학술논문

Excessive vascular sprouting underlies cerebral hemorrhage in mice lacking αVβ8-TGFβ signaling in the brain.
Document Type
article
Source
Development (Cambridge, England). 141(23)
Subject
Blood-Brain Barrier
Brain
Endothelial Cells
Animals
Mice
Cerebral Hemorrhage
Neovascularization
Pathologic
Transforming Growth Factor beta
Integrins
Microscopy
Confocal
Cell Count
Immunohistochemistry
Analysis of Variance
Signal Transduction
Angiogenesis
CNS
Hemorrhage
Integrin αVβ8
Mouse
Sprouting
TGFβ
Integrin alpha V beta 8
TGF beta
Neovascularization
Pathologic
Microscopy
Confocal
Stroke
Neurosciences
Stem Cell Research
Stem Cell Research - Nonembryonic - Non-Human
Brain Disorders
1.1 Normal biological development and functioning
2.1 Biological and endogenous factors
Cardiovascular
Biological Sciences
Medical and Health Sciences
Language
Abstract
Vascular development of the central nervous system and blood-brain barrier (BBB) induction are closely linked processes. The role of factors that promote endothelial sprouting and vascular leak, such as vascular endothelial growth factor A, are well described, but the factors that suppress angiogenic sprouting and their impact on the BBB are poorly understood. Here, we show that integrin αVβ8 activates angiosuppressive TGFβ gradients in the brain, which inhibit endothelial cell sprouting. Loss of αVβ8 in the brain or downstream TGFβ1-TGFBR2-ALK5-Smad3 signaling in endothelial cells increases vascular sprouting, branching and proliferation, leading to vascular dysplasia and hemorrhage. Importantly, BBB function in Itgb8 mutants is intact during early stages of vascular dysgenesis before hemorrhage. By contrast, Pdgfb(ret/ret) mice, which exhibit severe BBB disruption and vascular leak due to pericyte deficiency, have comparatively normal vascular morphogenesis and do not exhibit brain hemorrhage. Our data therefore suggest that abnormal vascular sprouting and patterning, not BBB dysfunction, underlie developmental cerebral hemorrhage.