The distribution of the proteoglycan FORSE-1 in the developing mouse central nervous system.
Albert KellyAisling O'MalleyMohammad RedhaGerard W O'KeeffeDenis S BarryPublished in: Journal of anatomy (2018)
Glycosylation is a major post-translational modification in which a carbohydrate known as a glycan is enzymatically attached to target proteins which regulate protein folding and stability. Glycans are strongly expressed in the developing nervous system where they play multiple roles during development. The importance of these glycan epitopes in neural development is highlighted by a group of conditions known as congenital disorders of glycosylation which lead to psychomotor difficulties, mental retardation, lissencephaly, microencephaly and epilepsy. One of these glycan epitopes, known as Lewis X, is recognised by the FORSE-1 antibody and is regionally expressed in the developing nervous system. In this study, we report the regional and temporal expression patterns of FORSE-1 immunolabelling during the periods of neurogenesis, gliogenesis and axonogenesis in developing mouse nervous system. We demonstrate the localisation of FORSE-1 on subsets of neuroepithelial cells and radial glial cells, and in compartments corresponding to axon tract formation. These spatial, temporal and regional expression patterns are suggestive of roles in the determination of different cell lineages and in the patterning of white matter during development, and help provide insights into the neuroanatomical regions affected by congenital disorders of glycosylation.
Keyphrases
- induced apoptosis
- poor prognosis
- white matter
- cell cycle arrest
- cell surface
- binding protein
- mental health
- multiple sclerosis
- cell death
- stem cells
- endoplasmic reticulum stress
- single cell
- small molecule
- single molecule
- oxidative stress
- molecular dynamics simulations
- mesenchymal stem cells
- long non coding rna
- cell proliferation
- protein protein
- peripheral blood
- mass spectrometry
- cerebrospinal fluid
- simultaneous determination
- tandem mass spectrometry