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Critical Examination of Muller Glia-Derived in vivo Neurogenesis in the Mouse Retina

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出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fcell.2022.830382

关键词

Muller glia; neurogenesis; mice; retina; fate mapping

资金

  1. National Institutes of Health [R01 EY024986, R01 EY028921]
  2. Research to Prevent Blindness
  3. Family Foundation for Vision Research

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This article discusses the regenerative potential of Muller glia (MG) in the mouse retina, focusing on the progress made in the de novo regeneration of retinal neurons through the reprogramming of MG.
Muller glia (MG) are a potential source of stem cells in the mammalian retina that could replenish lost retinal neurons for vision restoration. Unlike their counterpart in zebrafish, mammalian MG are quiescent and they do not spontaneously generate new retinal neurons. In recent years, extensive research efforts have been made to unlock the regenerative capabilities of Muller glia (MG) for de novo regeneration of retinal neurons in mice. Here, we discuss current research progress on MG-derived in vivo neurogenesis in the mouse retina, focusing on the use of stringent fate mapping techniques to evaluate and validate de novo regeneration of retinal neurons through the reprogramming of endogenous MG. Establishing stringent experimental criteria is critical for examining current and future studies on MG-derived regeneration of photoreceptors, retinal inter-neurons, and retinal ganglion cells.

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