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Abstract
Some of the most common causes of blindness involve the degeneration of photoreceptors
in the neural retina; photoreceptor replacement therapy might restore some vision
in these individuals. Embryonic stem cells (ESCs) could, in principle, provide a source
of photoreceptors to repair the retina. We have previously shown that retinal progenitors
can be efficiently derived from human ESCs. We now show that retinal cells derived
from human ESCs will migrate into mouse retinas following intraocular injection, settle
into the appropriate layers, and express markers for differentiated cells, including
both rod and cone photoreceptor cells. After transplantation of the cells into the
subretinal space of adult Crx(-/-) mice (a model of Leber's Congenital Amaurosis),
the hESC-derived retinal cells differentiate into functional photoreceptors and restore
light responses to the animals. These results demonstrate that hESCs can, in principle,
be used for photoreceptor replacement therapies.