Previous studies have shown that the fetal retina not only survives transpl
antation but also continues to develop and differentiate in the host eye. S
everal structural and functional proteins have been demonstrated in the tra
nsplanted retinas, and the presence of such proteins has been taken as evid
ence for the capability of retinal transplants to function. Glycine is an i
mportant inhibitory neurotransmitter and is found in a large number of the
retinal neurons. Uptake of glycine rather than de novo synthesis is the mai
n source of glycine in glycinergic neurons. The present study examined whet
her glycine-accumulating neurons develop normally in rabbit retina transpla
nts. Embryonic day (E) 15 rabbit retinas were transplanted into the eyes of
adult rabbits of the same strain. Transplants were allowed to survive for
various times so that the grafts attained the equivalent ages of (donor age
+ survival time) E 19, 22 and 29 and postnatal days (PN) 2, 5, 9, 12, 19 a
nd 58. On formaldehyde-fixed cryostat sections of these transplants, glycin
e-accumulating neurons were demonstrated by immunohistochemistry by using a
n antibody against one of the glycine transporters: GLYT1. Immunoreactivity
was first detected 2 days before birth and increased with age until it rea
ched its mature level at PN 19. The immunoreactivity was found in cells bel
onging to the inner retinal layers, and in plexiform layers of the transpla
nt equivalent to the normal inner and the outer plexiform layers. in places
these cells integrated well with similar cells in the host. In the host re
tina, the immunoreactivity was found in proximal cell layers of the inner n
uclear layer, in certain bipolar cells, and in the inner and the outer plex
iform layers. The immunoreactivity was preserved even in the degenerated re
tina overlying the retinal graft. In conclusion, the present study demonstr
ates that glycine-accumulating neurons develop, integrate and survive in re
tinal transplants.
Copyright (C) 2000 S. Karger AG, Basel.