nervous system
• in newborn homozygotes, a fraction of neuronal progenitors fail to colonize their target cortical layers III and II during cerebral cortex development; as a result, a greater number (~17%) of BrdU-labeled cells remain in the deeper cortical layers (VI-IV) and the corpus callosum relative to wild-type mice (~8.8%)
• this defect is variable, as many more BrdU-positive cells (25-36%) are found in the corpus callosum and deep layers of severely affected homozygotes, whereas a few others are indistinguishable from wild-type
• adult homozygotes display varying degrees of ectopic parvalbumin-positive neurons in the hippocampal commissure
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• adult homozygotes display varying degrees of ectopic parvalbumin-positive neurons in the hippocampal commissure located beneath the cerebral cortex
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• at birth, homozygotes show defects in organization and differentiation of the cerebral cortex
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• at birth, only a few differentiated, large pyramidal neurons are detected in the cerebral cortex
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• at birth, all differentiating cortical layers appear compressed and less distinct
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• an average reduction of ~25% in parvalbumin-positive neurons is observed in all cortical layers
• however, no differences in the distribution of astroglial cells are observed
• no significant differences are noted in cell survival in either embryonic (E16), newborn or adult cerebral cortex, as shown by TUNEL analysis
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• at birth, the thickness of the cerebral cortex is reduced by ~10%
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• adult homozygotes show neuronal abnormalities throughout the mantle layer of the cervical spinal cord, with only a few differentiated large neurons while all other neural cell types appear normal
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• adult homozygotes respond normally to chronic angiotensin II infusion but show an impaired baroreceptor reflex
• in response to an acute vasodilatory stimulus (isoproterenol), all homozygotes, but no wild-type mice, display a significant drop in blood pressure along with an impaired increase in heart rates, indicating autonomic dysfunction
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cardiovascular system
hypotension
(
J:49141
)
• on average, the blood pressure of adult homozygotes is reduced by ~10 mmHg relative to wild-type littermates
• however, no differences in baseline plasma renin values, heart rates or body weights are observed
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behavior/neurological
N |
• homozygotes do NOT develop seizures or reeler-like phenotypes
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hearing/vestibular/ear
N |
• homozygotes exhibit normal inner ear morphogenesis with no detectable abnormalities at the adult stage
• in addition, homozygotes show no significant differences in hearing thresholds before and after noise-induced cochlear damage relative to wild-type littermates
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cellular
• in newborn homozygotes, a fraction of neuronal progenitors fail to colonize their target cortical layers III and II during cerebral cortex development; as a result, a greater number (~17%) of BrdU-labeled cells remain in the deeper cortical layers (VI-IV) and the corpus callosum relative to wild-type mice (~8.8%)
• this defect is variable, as many more BrdU-positive cells (25-36%) are found in the corpus callosum and deep layers of severely affected homozygotes, whereas a few others are indistinguishable from wild-type
• adult homozygotes display varying degrees of ectopic parvalbumin-positive neurons in the hippocampal commissure
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