Brain abnormalities in immune defective mice
Mouse strains with or without disorders were examined in order to further assess the incidence of brain anomalities in immune-disordered strains. The brain was examined in Nissl-stained serial sections under a light microscope for the presence of abnormalities, with specific attention to ectopic col...
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Veröffentlicht in: | Brain research 1990-11, Vol.532 (1), p.25-33 |
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Sprache: | eng |
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Zusammenfassung: | Mouse strains with or without disorders were examined in order to further assess the incidence of brain anomalities in immune-disordered strains. The brain was examined in Nissl-stained serial sections under a light microscope for the presence of abnormalities, with specific attention to ectopic collections of neurons in layer I of the neocortex, as reported in the autoimmune New Zealand Black (NZB) and BXSB strains. The present study was designed to survey additional strains with immune disorders (Snell dwarf, C57BL/6J-
nu/nu, BALB/cByJ-
nu/nu, and SJL) and 7 control strains without immune disorders. In addition, we attempted to replicate past findings in the higly affected BXSB strain and the MRL/1 strain, which develops autoimmune disease, but has a low incidence of brain abnormalities. The largest number of brain abnormalities (20–40%) were seen in the C57BL/6J-
nu/nu, Snell dwarf and BXSB strains. The anomalies in the C57BL/6J-
nu/nu and BXSB mice consisted of ectopic neurons in layer I of the neocortex, whereas the Snell dwarf mice had either neuron-free areas in the cortex, or rippling of cortical layers II-IV, and one case had agenesis of the corpus callosum. Between 4% and 8% of the mice from the SJL, MRL/1, and MRL +/+ strains had either neuron-free areas in the cortex or ectopic neurons in layer I. The BALB/cByJ-
nu/nu and control strains did not have any cortical abnormalities. Future studies will be designed to determine whether immune-based alterations to the developing brain are responsible for the brain anomalies present in immune-disordered strains. |
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ISSN: | 0006-8993 1872-6240 |
DOI: | 10.1016/0006-8993(90)91737-2 |