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Permeable endothelium and the interstitial space of brain
1Laboratory of Neurobiology, National Institutes of Health, Bethesda, Maryland 20892-4062, USA. milt@codon.nih.gov
Cellular and Molecular Neurobiology
|March 4, 2000
Summary
Brain fenestrated vessels can be induced by agents stimulating urokinase. The brain
Area of Science:
- Neuroscience
- Vascular Biology
- Cell Biology
Background:
- Fenestrated vessels in the brain are typically absent but can be induced.
- Understanding the mechanisms and implications of brain fenestrated vessels is crucial for neurobiology.
- The blood-brain barrier's permeability is dynamically regulated.
Purpose of the Study:
- To investigate the induction of fenestrated vessels in the brain.
- To explore the role of urokinase and other factors in fenestrated vessel formation.
- To understand the solute transport and signaling mechanisms within the brain's interstitial spaces.
Main Methods:
- Agents stimulating urokinase production were used to induce fenestrated vessels.
- Analysis of solute transport through interstitial clefts and ventricular systems.
- Investigation of astrocyte gap junctions in volume transmission.
Main Results:
- Fenestrated vessels can be reversibly induced in the brain by agents that stimulate urokinase production.
- The glycocalyx and basal lamina are likely responsible for solute filtering in fenestrated vessels.
- Interstitial clefts serve as conduits for nonsynaptic volume transmission of signals and cell migration.
Conclusions:
- Urokinase, vascular endothelial growth factor, and metalloproteinases secreted by tumor cells may induce fenestrated vessels.
- The brain's cerebrospinal fluid (CSF) and interstitial clefts facilitate nonsynaptic volume transmission.
- Interstitial cleft characteristics change with brain maturation, impacting cell migration and solute transport.