Articles by Johanne Egge Rinholm in JoVE
Visualisierung und Live Imaging Oligodendrozyt Organellen in organotypischen Gehirnscheiben mit Adeno-assoziierten Virus und konfokale Mikroskopie Lauritz Hagen Kennedy1, Johanne Egge Rinholm1,2 1Division of Anatomy, Institute of Basic Medical Sciences, University of Oslo, 2Department of Microbiology, Oslo University Hospital Myelinating Oligodendrozyten fördern schnelle Aktionspotential Ausbreitung und neuronale überleben. Hier beschriebene ist ein Protokoll für Oligodendrozyt-spezifischen Ausdruck der fluoreszierende Proteine in organotypischen Gehirnscheiben mit nachfolgenden Zeitraffer Bildgebung. Darüber hinaus wird ein einfaches Verfahren zur Visualisierung von ungefärbten Myelin vorgestellt.
Other articles by Johanne Egge Rinholm on PubMed
LOC689986, a Unique Gene Showing Specific Expression in Restricted Areas of the Rodent Neocortex BMC Neuroscience. Jul, 2013 | Pubmed ID: 23844656 The neocortex is a highly specialised and complex brain structure, involved in numerous tasks, ranging from processing and interpretation of somatosensory information, to control of motor functions. The normal function linked to distinct neocortical areas might involve control of highly specific gene expression, and in order to identify such regionally enriched genes, we previously analysed the global gene expression in three different cortical regions (frontomedial, temporal and occipital cortex) from the adult rat brain. We identified distinct sets of differentially expressed genes. One of these genes, namely the hypothetical protein LOC689986 (LOC689986), was of particular interest, due to an almost exclusive expression in the temporal cortex.
Localisation of N-acetylaspartate in Oligodendrocytes/myelin Brain Structure & Function. Mar, 2015 | Pubmed ID: 24379086 The role of N-acetylaspartate in the brain is unclear. Here we used specific antibodies against N-acetylaspartate and immunocytochemistry of carbodiimide-fixed adult rodent brain to show that, besides staining of neuronal cell bodies in the grey matter, N-acetylaspartate labelling was present in oligodendrocytes/myelin in white matter tracts. Immunoelectron microscopy of the rat hippocampus showed that N-acetylaspartate was concentrated in the myelin. Also neuronal cell bodies and axons contained significant amounts of N-acetylaspartate, while synaptic elements and astrocytes were low in N-acetylaspartate. Mitochondria in axons and neuronal cell bodies contained higher levels of N-acetylaspartate compared to the cytosol, compatible with synthesis of N-acetylaspartate in mitochondria. In aspartoacylase knockout mice, in which catabolism of N-acetylaspartate is blocked, the levels of N-acetylaspartate were largely increased in oligodendrocytes/myelin. In these mice, the highest myelin concentration of N-acetylaspartate was found in the cerebellum, a region showing overt dysmyelination. In organotypic cortical slice cultures there was no evidence for N-acetylaspartate-induced myelin toxicity, supporting the notion that myelin damage is induced by the lack of N-acetylaspartate for lipid production. Our findings also implicate that N-acetylaspartate signals on magnetic resonance spectroscopy reflect not only vital neurons but also vital oligodendrocytes/myelin.