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Bral1: its role in diffusion barrier formation and conduction velocity in the CNS
Y Bekku, L Vargova, Y Goto, I Vorisek, L Dmytrenko, M Narasaki, A Ohtsuka, R Fassler, Y Ninomiya, E Sykova, T Oohashi
Language English Country United States
Document type Research Support, Non-U.S. Gov't
Grant support
NS9915
MZ0
CEP Register
Digital library NLK
Full text - Article
Source
NLK
Free Medical Journals
from 1981 to 6 months ago
PubMed Central
from 1981 to 6 months ago
Europe PubMed Central
from 1981 to 6 months ago
Open Access Digital Library
from 1981-01-01
Open Access Digital Library
from 1981-01-01
- MeSH
- Action Potentials * physiology MeSH
- Cell Membrane metabolism MeSH
- Central Nervous System * metabolism ultrastructure MeSH
- Diffusion MeSH
- Diffusion Magnetic Resonance Imaging MeSH
- Extracellular Matrix metabolism MeSH
- Ion Channel Gating physiology MeSH
- Ion Channels metabolism MeSH
- Cations metabolism MeSH
- Hyaluronic Acid metabolism MeSH
- Mice, Inbred ICR MeSH
- Mice, Knockout MeSH
- Mice MeSH
- Nerve Fibers, Myelinated * metabolism ultrastructure MeSH
- Neural Conduction * physiology MeSH
- Nerve Tissue Proteins genetics metabolism MeSH
- Proteoglycans genetics metabolism MeSH
- Ranvier's Nodes * metabolism ultrastructure MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Mice MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Research Support, Non-U.S. Gov't MeSH
At the nodes of Ranvier, excitable axon membranes are exposed directly to the extracellular fluid. Cations are accumulated and depleted in the local extracellular nodal region during action potential propagation, but the impact of the extranodal micromilieu on signal propagation still remains unclear. Brain-specific hyaluronan-binding link protein, Bral1, colocalizes and forms complexes with negatively charged extracellular matrix (ECM) proteins, such as versican V2 and brevican, at the nodes of Ranvier in the myelinated white matter. The link protein family, including Bral1, appears to be the linchpin of these hyaluronan-bound ECM complexes. Here we report that the hyaluronan-associated ECM no longer shows a nodal pattern and that CNS nerve conduction is markedly decreased in Bral1-deficient mice even though there were no differences between wild-type and mutant mice in the clustering or transition of ion channels at the nodes or in the tissue morphology around the nodes of Ranvier. However, changes in the extracellular space diffusion parameters, measured by the real-time iontophoretic method and diffusion-weighted magnetic resonance imaging (MRI), suggest a reduction in the diffusion hindrances in the white matter of mutant mice. These findings provide a better understanding of the mechanisms underlying the accumulation of cations due to diffusion barriers around the nodes during saltatory conduction, which further implies the importance of the Bral1-based extramilieu for neuronal conductivity.
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Literatura
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- $a At the nodes of Ranvier, excitable axon membranes are exposed directly to the extracellular fluid. Cations are accumulated and depleted in the local extracellular nodal region during action potential propagation, but the impact of the extranodal micromilieu on signal propagation still remains unclear. Brain-specific hyaluronan-binding link protein, Bral1, colocalizes and forms complexes with negatively charged extracellular matrix (ECM) proteins, such as versican V2 and brevican, at the nodes of Ranvier in the myelinated white matter. The link protein family, including Bral1, appears to be the linchpin of these hyaluronan-bound ECM complexes. Here we report that the hyaluronan-associated ECM no longer shows a nodal pattern and that CNS nerve conduction is markedly decreased in Bral1-deficient mice even though there were no differences between wild-type and mutant mice in the clustering or transition of ion channels at the nodes or in the tissue morphology around the nodes of Ranvier. However, changes in the extracellular space diffusion parameters, measured by the real-time iontophoretic method and diffusion-weighted magnetic resonance imaging (MRI), suggest a reduction in the diffusion hindrances in the white matter of mutant mice. These findings provide a better understanding of the mechanisms underlying the accumulation of cations due to diffusion barriers around the nodes during saltatory conduction, which further implies the importance of the Bral1-based extramilieu for neuronal conductivity.
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