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Late-Stage Neuronal Progenitors in the Retina Are Radial Müller Glia That Function as Retinal Stem Cells

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TLDR
It is concluded that zebrafish Müller glia function as multipotent retinal stem cells that generate retinal neurons by homeostatic and regenerative developmental mechanisms.
Abstract
Neuronal progenitors in the mammalian brain derive from radial glia or specialized astrocytes. In developing neural retina, radial glia-like Muller cells are generated late in neurogenesis and are not considered to be neuronal progenitors, but they do proliferate after injury and can express neuronal markers, suggesting a latent neurogenic capacity. To examine the neurogenic capacity of retinal glial cells, we used lineage tracing in transgenic zebrafish with a glial-specific promoter (gfap, for glial fibrillary acid protein) driving green fluorescent protein in differentiated Muller glia. We found that all Muller glia in the zebrafish retina express low levels of the multipotent progenitor marker Pax6 (paired box gene 6), and they proliferate at a low frequency in the intact, uninjured retina. Muller glia-derived progenitors express Crx (cone rod homeobox) and are late retinal progenitors that generate the rod photoreceptor lineage in the postembryonic retina. These Muller glia-derived progenitors also remain competent to produce earlier neuronal lineages, in that they respond to loss of cone photoreceptors by specifically regenerating the missing neurons. We conclude that zebrafish Muller glia function as multipotent retinal stem cells that generate retinal neurons by homeostatic and regenerative developmental mechanisms.

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The molecular basis of retinal ganglion cell death in glaucoma.

TL;DR: This body of work has considerably updated and expanded the view of how RGCs might die in glaucoma and has revealed novel, potential targets for neuroprotection.
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Cellular signaling and factors involved in Müller cell gliosis: neuroprotective and detrimental effects.

TL;DR: An overview of the neuroprotective and detrimental effects of Müller cell gliosis is provided, with accounts on the cellular signal transduction mechanisms and factors which are implicated in Müllercell-mediated neuroprotection, immunomodulation, regulation of Müllers cell proliferation, upregulation of intermediate filaments, glial scar formation, and the generation of neural progenitor/stem cells.
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New functions of Müller cells.

TL;DR: This review gives a survey of recently discoved new functions of Müller cells, living optical fibers that guide light through the inner retinal tissue that enhance the signal/noise ratio by minimizing intraretinal light scattering and conserve the spatial distribution of light patterns in the propagating image.
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Muller glial cell reprogramming and retina regeneration

TL;DR: In teleost fish, the response of Müller 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.
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The zebrafish as a model for complex tissue regeneration

TL;DR: Zebrafish studies have helped identify new mechanistic underpinnings of regeneration in multiple tissues and, in some cases, have served as a guide for contemplating regenerative strategies in mammals.
References
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Mode of cell migration to the superficial layers of fetal monkey neocortex.

TL;DR: Golgi and electronmicroscopic methods were used to define the shapes and intercellular relationships of cells migrating from their sites of origin near the ventricular surface across the intermediate zone to the superficial neocortical layers of the parietooccipital region in the brains of 75‐ to 97‐day monkey fetuses.
Journal ArticleDOI

Neurons derived from radial glial cells establish radial units in neocortex

TL;DR: The results support the concept that a lineage relationship between neurons and proliferative radial glia may underlie the radial organization of neocortex.
Journal ArticleDOI

The cell biology of neurogenesis.

TL;DR: In this paper, the authors discuss how these features change during development from neuroepithelial to radial glial cells, and how this transition affects cell fate and neurogenesis.
Book

Müller Cells in the Healthy and Diseased Retina

TL;DR: A proper understanding of the gliotic responses of Müller cells in the diseased retina, and of their protective vs. detrimental effects, is essential for the development of efficient therapeutic strategies that use and stimulate the neuron-supportive/protective-and prevent the destructive-mechanisms of gliosis.
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