Neuronal Dystroglycan Is Necessary for Formation and Maintenance of Functional CCK-Positive Basket Cell Terminals on Pyramidal Cells.
Simon FrühJennifer RomanosPatrizia PanzanelliDaniela BürgisserShiva K TyagarajanKevin P CampbellMirko SantelloJean-Marc FritschyPublished in: The Journal of neuroscience : the official journal of the Society for Neuroscience (2017)
Dystroglycan, an extracellular and transmembrane protein of the dystrophin-glycoprotein complex, is at the center of molecular studies of muscular dystrophies. Although its synaptic distribution in cortical brain regions is long established, function of dystroglycan in the synapse remained obscure. Using mice that selectively lack neuronal dystroglycan, we provide evidence that a subset of GABAergic interneurons requires dystroglycan for formation and maintenance of axonal terminals on pyramidal cells. As such, dystroglycan is the first postsynaptic GABAergic protein for which an interneuron terminal-specific function could be shown. Our findings also offer a new perspective on the mechanisms that lead to intellectual disability in muscular dystrophies without associated brain malformations.
Keyphrases
- intellectual disability
- induced apoptosis
- cell cycle arrest
- cerebral ischemia
- autism spectrum disorder
- resting state
- white matter
- resistance training
- single cell
- protein protein
- spinal cord injury
- oxidative stress
- signaling pathway
- functional connectivity
- metabolic syndrome
- amino acid
- duchenne muscular dystrophy
- type diabetes
- stem cells
- cell death
- cell therapy
- cell proliferation
- skeletal muscle