Monolayer properties of nervous system lipids.
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Biomedical subjects
Publications and source records attributed to M L Cuzner.
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1. The turnover of lipids, of myelin and other brain subcellular particles has been studied in double-labelling experiments on intact rats. 2. Overall metabolism of brain mitochondrial lipids was three times slower than that of the liver. 3. Individual lipids of brain mitochondria and myelin were also separated and their metabolism was studied. 4. All myelin lipids examined undergo very slow turnover. Two pools of brain mitochondrial lipid were identified. The slowly metabolized lipids were cholesterol, cardiolipin plus phosphatidic acid and possibly sphingomyelin; the remaining phosphatides underwent more rapid turnover. 5. The possible significance of these results is discussed.
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As there is evidence of early biochemical and histological changes in the normal-appearing white matter in MS, which appear to be independent of or precede demyelination, the formation of plaques may be incidental to a more primary lesion. The finding of persistently increased levels of IgG in the CSF of patients with MS points to an ongoing immune reaction in the CNS, possible against an infective agent; but virus-specific antibodies account for only a small proportion of IgG in the CSF. Furthermore, in vitro assays of T cell function suggest that there may be a regulator T cell defect in MS. Salk and colleagues (1980) have postulated that MS may be a disorder, attributable to multiple inducing agents, which is potentiated through deregulation of lymphocyte function.
Primary cultures were established from autopsy or biopsy samples of normal adult human brain and characterized by immunocytochemical techniques. Initially, macrophages were the predominant cell type adhering to the substratum, but as their number fell that of glial cells increased. Oligodendrocytes comprised 30% of the glial population in white matter cultures, and their perikarya and elongated processes were immunostained with antibodies directed against galactocerebroside and four myelin proteins. In white and grey matter cultures, process-bearing astrocytes and small numbers of polygonal astrocytes were stained with antibodies against glial fibrillary acidic protein and glutamine synthetase. Fibroblasts started to appear at 3 weeks and proliferated to form a monolayer beneath glial cells by 5 weeks. Glia began to die in the 6th week. These primary cell cultures of white or grey matter can be used to study the properties of glial cells from normal or pathological adult human brain.