mortality/aging
N |
• unlike germline null mice, mice are viable
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nervous system
• elevated levels of apoptosis markers indicating increased Purkinje cell death
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• decrease in the amount of plasma membrane AMPA-type glutamate receptor subunits in the postsynaptic density fraction from the cerebellum
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• degeneration is first seen in lobules X and IX at 3 weeks of age and then spreads to other regions with age
• however, no degeneration of neurons is seen in the molecular or granule layers of the cerebellum
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• decrease in dendrite size and arborization at P30
• dendrites at P30 are smaller than those at P9 indicating both failure to grow and atrophy
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• loss of Purkinje cells beginning at 3 weeks of age
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• becomes thinner with age in correlation with loss of Purkinje cells
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• dramatically reduced in size
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cellular
• compaction of the Golgi apparatus at P14 and P28 in Purkinje cells and a similar disruption is seen in granule cells in the cerebellum
• absence of Golgi outposts in primary dendrites of Purkinje cells at P8
• Golgi apparatus is located on the opposite side of the soma to the primary dendrite and the apparatus is dissociated from the centrosome indicating a loss of Golgi polarity in Purkinje cells at P14 and P28
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• loss of cisternal stacking and cisternal length and an accumulation of vesicular profiles localized to the perinuclear region
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• elevated levels of apoptosis markers indicating increased Purkinje cell death
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• impaired secretory trafficking
• reduced soma to dendrite trafficking of GRIA2 in Purkinje cells
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behavior/neurological
• limp reflex when lifted by the tail
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• ataxic gait
• coordination defects are mild in young mice and progressively worsen with age
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• slight reduction in time spent on a rotarod at 3 weeks of age and this reduction becomes more profound with age (8 and 12 weeks)
• require more time to cross balance beams of multiple sizes
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growth/size/body
• growth retardation is less than that in germline null mice
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