Biology and therapy of inherited retinal degenerative disease: insights from mouse models

Retinal neurodegeneration associated with the dysfunction or death of photoreceptors is a major cause of incurable vision loss. Tremendous progress has been made over the last two decades in discovering genes and genetic defects that lead to retinal diseases. The primary focus has now shifted to unc...

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Vydáno v:	Disease models & mechanisms Ročník 8; číslo 2; s. 109 - 129
Hlavní autoři:	Veleri, Shobi, Lazar, Csilla H., Chang, Bo, Sieving, Paul A., Banin, Eyal, Swaroop, Anand
Médium:	Journal Article
Jazyk:	angličtina
Vydáno:	England The Company of Biologists Ltd 01.02.2015 The Company of Biologists Limited The Company of Biologists
Témata:	Animals Disease Disease Models, Animal Genes Genetic Diseases, Inborn - therapy Humans Light Signal Transduction Macular degeneration Mice Mouse mutants Mutation Photoreceptor Photoreceptor Cells, Vertebrate - pathology Photoreceptors Proteins Retina Retina - pathology Retina - physiopathology Retinal Degeneration - therapy Retinal development Retinal disease Review Retinal development Mouse mutants Retinal disease Photoreceptor
ISSN:	1754-8403, 1754-8411, 1754-8411
On-line přístup:	Získat plný text
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Popis
Shrnutí:	Retinal neurodegeneration associated with the dysfunction or death of photoreceptors is a major cause of incurable vision loss. Tremendous progress has been made over the last two decades in discovering genes and genetic defects that lead to retinal diseases. The primary focus has now shifted to uncovering disease mechanisms and designing treatment strategies, especially inspired by the successful application of gene therapy in some forms of congenital blindness in humans. Both spontaneous and laboratory-generated mouse mutants have been valuable for providing fundamental insights into normal retinal development and for deciphering disease pathology. Here, we provide a review of mouse models of human retinal degeneration, with a primary focus on diseases affecting photoreceptor function. We also describe models associated with retinal pigment epithelium dysfunction or synaptic abnormalities. Furthermore, we highlight the crucial role of mouse models in elucidating retinal and photoreceptor biology in health and disease, and in the assessment of novel therapeutic modalities, including gene- and stem-cell-based therapies, for retinal degenerative diseases.
Bibliografie:	ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Review-3 content type line 23
ISSN:	1754-8403 1754-8411 1754-8411
DOI:	10.1242/dmm.017913