WE have investigated the expression and cellular localization of ciliary ne
urotrophic factor (CNTF) in the rat retina following ischemia induced by tr
ansiently increasing the intraocular pressure. In the normal retina, CNTF i
mmunoreactivity was restricted to profiles in the ganglion cell layer. Foll
owing ischemia and reperfusion, immunoreactivity appeared in Muller cell so
mata and processes and its intensity increased between 1 day and 2 weeks po
st-lesion. Quantitative evaluation by immunoblotting confirmed that CNTF ex
pression continuously increased up to 2 weeks after ischemic injury (to 600
% of control levels), but had declined again to 250% of controls at 4 weeks
post-lesion, Our findings suggest that CNTF supplied by Muller cells has a
protective function for lesioned neurons following transient ischemia. (C)
1999 Lippincott Williams & Wilkins.