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Muller glial cell reprogramming and retina regeneration

Journal

NATURE REVIEWS NEUROSCIENCE
Volume 15, Issue 7, Pages 431-442

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nrn3723

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Funding

  1. NEI, US National Institute of Health [RO1 EY 018132, 1R21 EY022707]
  2. Research to Prevent Blindness

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Muller glia are the major glial component of the retina. They are one of the last retinal cell types to be born during development, and they function to maintain retinal homeostasis and integrity. In mammals, Muller glia respond to retinal injury in various ways that can be either protective or detrimental to retinal function. Although these cells can be coaxed to proliferate and generate neurons under special circumstances, these responses are meagre and insufficient for repairing a damaged retina. By contrast, in teleost fish (such as zebrafish), the response of Muller glia to retinal injury involves a reprogramming event that imparts retinal stem cell characteristics and enables them to produce a proliferating population of progenitors that can regenerate all major retinal cell types and restore vision. Recent studies have revealed several important mechanisms underlying Muller glial cell reprogramming and retina regeneration in fish that may lead to new strategies for stimulating retina regeneration in mammals.

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