Inherited retinal degenerations such as retinitis pigmentosa (RP) are chara
cterized by progressive loss of photoreceptors, apparently by apoptosis, an
d our recent report of increased secreted Frizzed-related protein-2 (SFRP2)
in RP retinas suggests altered Wnt signalling may be a component of the de
generative process. The present study shows that levels of SFRP1, SFRP3 and
SFRP5 mRNAs are also abnormal in RP, giving rise to idiosyncratic expressi
on patterns. In highly degenerative retinas, the SFRP proteins localize mai
nly to the inner limiting membrane, but in a well-preserved retina SFRP1 an
d SFRP5 are notably localized to the surviving photoreceptors. Together wit
h increased c-jun mRNA expression in all cases examined, these results supp
ort the notion that disruptions of Wnt network signalling are involved in r
etinal neurodegeneration. NeuroReport 11:3963-3967 (C) 2000 Lippincott Will
iams & Wilkins.