vision/eye
• outer retinal thickness is already reduced at P15 and thereafter declines
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• activated Muller cell processes are seen across the outer nuclear layer
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• retinal schisis is apparent until later adult stages when it becomes less apparent
• schisis severity peaks at P15
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• cone pedicles are malformed
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• cone outer segments are shortened
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• dark-adapted ERG is reduced in amplitude
• the light-adapted cone ERG is reduced in amplitude at P15, P24, and 10 weeks of age
• the b-wave is reduced more than the a-wave, indicating a negative ERG waveform
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• dark-adapted a-wave amplitude is reduced at P15, P24, and 10 weeks of age
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• dark-adapted b-wave amplitude is reduced at P15, P24, and 10 weeks of age with the greatest ERG b-wave reduction at P15 and P24
• light-adapted b-wave amplitude is reduced at P15, P24, and 10 weeks of age
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• retinal ganglion cell electrophysiology shows elevated activity in the absence of a visual stimulus and reduced signal-to-noise ratios in response to light stimuli
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nervous system
• activated Muller cell processes are seen across the outer nuclear layer
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• density of astrocyte processes is increased, reflecting either increased numbers or activation of the cells
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• numerous dendritic processes of synaptotagmin II+ bipolar cells invade the outer nuclear layer indicating aberrant sprouting
• ectopic outer nuclear layer sprouting of cone bipolar cells
• cone bipolar cell projections into the inner nuclear layer are seen
• aberrant sprouting is also seen in rod bipolar cells and PKC+ rod bipolar cell dendrites are seen to extend toward and into the outer nuclear layer
• calbindin+ horizontal cells extend their neurites into the outer nuclear layer compared to their normal termination in the outer plexiform layer in wild-type mice
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• cone pedicles are malformed
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• cone outer segments are shortened
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• retinal ganglion cells (RGCs) show an increase in spontaneous firing rate, in both ON- and OFF-type RGCs
• both excitatory and inhibitory inputs show aberrant activity in retinal ganglion cells
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Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
X-linked juvenile retinoschisis 1 | DOID:0060763 |
OMIM:312700 |
J:285517 |