BRAIN ABNORMALITIES IN IMMUNE DEFECTIVE MICE

被引:85
作者
SHERMAN, GF
MORRISON, L
ROSEN, GD
BEHAN, PO
GALABURDA, AM
机构
[1] HARVARD UNIV, SCH MED, DEPT NEUROL, BOSTON, MA 02115 USA
[2] BETH ISRAEL HOSP, CHARLES A DANA RES INST, BOSTON, MA 02215 USA
[3] UNIV GLASGOW, DEPT NEUROL, GLASGOW G12 8QQ, SCOTLAND
[4] SO GEN HOSP, INST NEUROL SCI, GLASGOW G51 4TF, SCOTLAND
关键词
Autoimmunity; Cerebral cortex; Developmental dyslexia; Dysplasia; Ectopia; Neuronal migration;
D O I
10.1016/0006-8993(90)91737-2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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. © 1990.
引用
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页码:25 / 33
页数:9
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