“…GFAP is the major compo nent of glial intermediate filaments found in astrocytes and has been generally accepted as an astrocyte-specific cell marker [1], In the retina of land vertebrates, GFAP is only present in the end-foot of Müller cells, if at all [2], However, Müller cells accumulate GFAP in response to retinopathy of prematurity [3], penetrating ocular injury [4], lensectomy-vitrectomy [5], light damage [6][7][8][9][10], aging [11], glaucoma [12], gliosis [13], experimental reti nal detachment [12,14], reduced ocular blood flow [15,16] and inherited retinal dystrophy [6,17], and elaborate an extensive network of glial filaments throughout their cytoplasm. This increase in intermediate filament is in herent in the reactive gliosis process and is thought to stabilise the new and enlarged glial processes which extend into the space left by the degenerating photoreceptors [14], Both focused laser irradiation of short du ration (milliseconds) [8,9] and prolonged ex posure (hours) to diffuse light of low energy [6,7,10] induce retinal lesions. In our labora tory, low intensity diffuse white fluorescent light (1,000 lx for 2 h) is used to induce retinal photoreceptor damage in albino rats.…”