mortality/aging
• mice die between E16.5 and P0 with a number of defects including intraamniotic hemorrhage, hydrops fetalis and frequent exencephaly
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nervous system
• aberrant extensions of radial processes into ectopic growths are observed
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• mice lack uDTI staining in the intermediate zone (IZ) indicating an absence of organized axon tracts
• the IZ is thinner than in wild-type mice
• IZ cortices are nearly devoid of neurofilament protein + axons
Tau-1 staining is reduced
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• the cortices show cortical neurons pouring through gaps in the pial membrane and spreading tangentially within the subarachnoid space compared to the well organized cortical plate and intact pial membrane in wild-type mice
• however, laminin staining surrounding ectopias is normal and in regions without ectopias cortical plate architecture is preserved
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hydrocephaly
(
J:127447
)
• mice display hydrocephalus ex vacuo
|
• at E18.5, mice display enlarged ventricle size
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• all cortical fiber tracts are missing from the brain, including all major forebrain commissures and the internal capsule
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• gaps in the pial membrane allow spread of cortical neurons into the subarachnoid space
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• contains ectopic cortical neurons
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exencephaly
(
J:127447
)
• between E16.5 and P0, mice frequently display exenchephaly
|
• after 48 hours in culture, 74% of neuritis are at stage 2 of neuritogenesis with only 2% at stage 3 compared to 10% of wild-type cells at stage 1 and 69% at stage 3
• however, axonal polarization is normal
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• at E18.5, mice exhibit cortical ectopias
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homeostasis/metabolism
• between E16.5 and P0
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cardiovascular system
hemorrhage
(
J:127447
)
• between E16.5 and P0 mice exhibit intraaminotic hemorrhage
|
cellular
• aberrant extensions of radial processes into ectopic growths are observed
|