The retina consists of various cell types arranged in eight cell layers and two membranes
that originate from the neuroectodermal cells. In this study, the timing of differentiation
and distribution of the cellular components and the layers of the rabbit
retina are investigated using light and electron microscopy and immunohistochemical
techniques. There were 32 rabbit embryos and 12 rabbits used. The rabbit retina
begins its prenatal development on the 10th day of gestation in the form of optic
cup. The process of neuro- and gliogenesis occurs in several stages: In the first stage,
the ganglionic cells are differentiated at the 15th day. The second stage includes the
differentiation of Muller, amacrine, and cone cells on the 23rd day. The differentiation
of bipolar, horizontal, and rod cells and formation of the inner segments of the
photoreceptors consider the late stage that occurs by the 27th and 30th day of gestation.
On the first week of age postnatally, the outer segments of the photoreceptors
are developed. S100 protein is expressed by the Muller cells and its processes
that traverse the retina from the outer to the inner limiting membranes. Calretinin is
intensely labeled within the amacrine and displaced amacrine cells. Ganglionic cells
exhibited moderate immunoreactivity for calretinin confined to their cytoplasm and
dendrites. In conclusion, all stages of neuro- and gliogenesis of the rabbit retina occur
during the embryonic period. Then, the retina continues its development postnatally
by formation of the photoreceptor outer segments and all layers of the retina
become established.