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by Bill Snyder<\/em><\/p>\n The tiny zebrafish may hold the secret to regenerating damaged retinas in humans, Vanderbilt University researchers reported last week in the journal Cell Reports<\/em>.<\/p>\n Currently there are few effective treatments for retinal degenerative diseases such as age-related macular degeneration (AMD), the most common cause of blindness in millions of Americans over age 55. The prognosis is equally dim for another 100,000 Americans with retinitis pigmentosa. Many of them are legally blind by age 40.<\/p>\n Mammals cannot spontaneously regenerate retinal neurons that are lost or damaged by disease. But in bony fish like the 1-inch-long zebrafish, which is widely used as a \u201cmodel organism\u201d in biological and medical research studies, retinal damage triggers a spontaneous regenerative response that restores both retinal structure and function.<\/p>\n Since the cells and structure of the retina are highly conserved among vertebrates, from fish to humans, understanding how zebrafish regenerate damaged retinas could lead to new ways to enhance retinal regeneration in people.<\/p>\n One key factor explored by James Patton, PhD, and colleagues in the Department of Biological Sciences at Vanderbilt University is a microRNA, miR-216a<\/em>, which regulates the expression of Dot1l, an enzyme involved in regulating gene expression.<\/p>\n Suppressing miR-216a<\/em>, they showed, initiates the differentiation and proliferation of M\u00fcller glia (MG)<\/em>, the source of regenerated neurons in the zebrafish retina, in part by releasing inhibition of Dot1l. A next step is to test whether suppressing miR-216a<\/em> can induce MG reprogramming and proliferation in mammals.<\/p>\n \u201cM\u00fcller glia constitute an adult stem cell in the zebrafish retina and our goal is to identify pathways and genes that could be activated to induce similar behavior in the human retina,\u201d said Patton, Stevenson Professor of Biological Sciences and director of the Interdisciplinary Graduate Program at Vanderbilt.<\/p>\n Patton\u2019s co-authors were graduate students Nergis Kara, Matthew Kent and Kamya Rajaram, Dominic Didiano, PhD, research associate professor of Biological Sciences, and undergraduate students Anna Zhao and Emily Summerbell.<\/p>\n The research was supported by National Eye Institute (NEI) grants EY024354 and EY019759, by Vanderbilt Vision Research Center Core Grant EY008126 and by an \u201cAudacious Goals Initiative\u201d grant (EY027265) aimed at finding ways to restore vision by regenerating neurons and their connections in the eye and visual system.<\/p>\n \u00a0<\/p>\n<\/div>\n