EFFECTS OF BASIC FIBROBLAST GROWTH-FACTOR ON THE RETINAL DEGENERATIONOF THE MI(VIT) MI(VIT) (VITILIGO) MOUSE - A MORPHOLOGIC AND ELECTROPHYSIOLOGIC STUDY/
Sb. Smith et al., EFFECTS OF BASIC FIBROBLAST GROWTH-FACTOR ON THE RETINAL DEGENERATIONOF THE MI(VIT) MI(VIT) (VITILIGO) MOUSE - A MORPHOLOGIC AND ELECTROPHYSIOLOGIC STUDY/, Experimental Eye Research, 63(5), 1996, pp. 565-577
Basic fibroblast growth factor (bFGE) has been shown to rescue dying p
hotoreceptor cells in the RCS rat, a model with a genetic defect of th
e RPE that impairs outer segment phagocytosis. The purpose of the pres
ent study was to determine whether intravitreal injection of bFGF woul
d have a similar effect on photoreceptor cell death in the vitiligo (C
57BL/6-mi(vit)/mi(vit)) mouse. This mutant mouse loses photoreceptor c
ells slowly over many months. Experimental evidence suggests that the
primary cellular site of the defect is the RPE. In the present study,
bFGF was prepared with and without heparin in PBS and injected intravi
treally into vitiligo mice at ages 2, 4, 6, 8 and 13 weeks, surroundin
g the onset of photoreceptor cell death. Non-injected, PBS-injected an
d heparin/PBS injected mice served as controls. Scotopic ERG's were pe
rformed on one group of mice prior to killing. Mice were killed 4, 6 o
r 10 weeks following the injection and the eyes were processed for his
tology and analysed. The amplitude of the b-wave was significantly sma
ller in mice injected with bFGP/PBS than in PBS-injected and non-injec
ted eyes regardless of the time of injection or duration following inj
ection. Histological examination revealed that the number of rows of p
hotoreceptor cells did not differ significantly between bFGF-injected,
vehicle- or non-injected mice. Although slight improvement in the att
achment of outer segments to RPE was observed in 4 week mutants inject
ed with bFGF/heparin/PBS, a similar result was obtained in heparin/PBS
injected mutants. In mice injected with bFGF without heparin, detachm
ent was severe and gross disruption of neural retina was observed. The
re were significantly more macrophages and photoreceptor cells in the
subretinal space in bFGF injected mice. It appears that at the dosages
and times administered, bPGF does not improve the electrophysiologica
l functioning of the retina nor retard the degeneration of the retina
in the vitiligo mouse as it does in the RCS rat. (C) 1996 Academic Pre
ss Limited