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Molecularly defined cortical astroglia subpopulation modulates neurons via secretion of Norrin
- Source :
- Nature neuroscience
- Publication Year :
- 2019
-
Abstract
- Despite expanding knowledge regarding the role of astroglia in regulating neuronal function, little is known about regional or functional subgroups of brain astroglia and how they may interact with neurons. We use an astroglia-specific promoter fragment in transgenic mice to identify an anatomically defined subset of adult gray matter astroglia. Using transcriptomic and histological analyses, we generate a combinatorial profile for the in vivo identification and characterization of this astroglia subpopulation. These astroglia are enriched in mouse cortical layer V; express distinct molecular markers, including Norrin and leucine-rich repeat-containing G-protein-coupled receptor 6 (LGR6), with corresponding layer-specific neuronal ligands; are found in the human cortex; and modulate neuronal activity. Astrocytic Norrin appears to regulate dendrites and spines; its loss, as occurring in Norrie disease, contributes to cortical dendritic spine loss. These studies provide evidence that human and rodent astroglia subtypes are regionally and functionally distinct, can regulate local neuronal dendrite and synaptic spine development, and contribute to disease.
- Subjects :
- 0301 basic medicine
Genetically modified mouse
Male
Dendritic spine
Transgene
Dendritic Spines
Mice, Transgenic
Nerve Tissue Proteins
Biology
Article
Receptors, G-Protein-Coupled
Transcriptome
03 medical and health sciences
0302 clinical medicine
Premovement neuronal activity
Animals
Humans
Secretion
Gray Matter
Receptor
Eye Proteins
Cells, Cultured
Cerebral Cortex
Neurons
LGR6
General Neuroscience
Motor Cortex
Mice, Inbred C57BL
030104 developmental biology
nervous system
Astrocytes
Neuroscience
030217 neurology & neurosurgery
Subjects
Details
- Language :
- English
- ISSN :
- 15461726 and 10976256
- Volume :
- 22
- Issue :
- 5
- Database :
- OpenAIRE
- Journal :
- Nature neuroscience
- Accession number :
- edsair.doi.dedup.....cf870c6bdaee8cb33cebcfc123833379