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Abstract
Mice lacking intrinsically photosensitive retinal ganglion cells (ipRGCs) retain pattern vision but show significant deficits in both pupillary light reflex (PLR) and circadian photoentrainment.
- Animals without ipRGCs demonstrate impairments in PLR and circadian photoentrainment that exceed those seen in melanopsin knockout mice.
- Deficits in these non-image-forming functions resemble those in animals lacking phototransduction across all three photoreceptor types.
- Retinal ganglion cells dissociate light signals for detecting light intensity from those used for pattern vision.
- Despite the inability to detect light for non-image-forming functions, these animals can still form images.
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