In humans, an increasing density of foveal cone
photoreceptors occurs slowly over several years after birth,
and accounts for a region that subserves high visual acuity.
Concurrently, inner retinal cells move centrifugally away
from the foveal center. Such developmental rearrangements
reflect complex cellular remodeling after the retinal neuronal
cells have differentiated and have formed synapses. Explaining
foveal morphogenesis is difficult, because differentiated
neuronal cells seem incapable of moving actively. Presented
here is a biomechanical explanation of how the above events
occur. This hypothesis assumes that the cellular movements
throughout the retinal layers occur passively as the eye
grows and the retina is stretched. Retinal stretch was
simulated using virtual engineering models that were analyzed
with finite element analysis. A pit combined with retinal
stretch causes the retinal layers to deform in a way that
accounts for both the centrifugal and centripetal movement
of various retinal cell types. Axially directed, tensile
forces associated with stretching the retinal tissue surrounding
the pit also accounts for the elongated morphology of foveal
cone photoreceptors. These simulations suggest that a pit
is required for both the centripetal displacement of cone
cells toward the center of the fovea, and for the elongated
foveal cone morphology. Since the primate fovea may have
minimal impact on acuity, its primary role may be to initiate
foveal morphogenesis in slowly developing eyes.