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Stem Cell–Derived Photoreceptor Transplants Differentially Integrate Into Mouse Models of Cone-Rod Dystrophy
Author(s) -
Tiago SantosFerreira,
Manuela Völkner,
Oliver Borsch,
Jochen Haas,
Peter Cimalla,
Praveen Vasudevan,
Peter Carmeliet,
Denis Corbeil,
Stylianos Michalakis,
Edmund Koch,
Michael Karl,
Marius Ader
Publication year - 2016
Publication title -
investigative ophthalmology and visual science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.935
H-Index - 218
eISSN - 1552-5783
pISSN - 0146-0404
DOI - 10.1167/iovs.16-19087
Subject(s) - retinitis pigmentosa , photoreceptor cell , retinal degeneration , biology , transplantation , microbiology and biotechnology , retina , rhodopsin , retinal regeneration , induced pluripotent stem cell , stem cell , retinal , ribbon synapse , regeneration (biology) , visual phototransduction , embryonic stem cell , pathology , neuroscience , medicine , genetics , biochemistry , vesicle , membrane , gene , synaptic vesicle
Preclinical studies on photoreceptor transplantation provided evidence for restoration of visual function with pluripotent stem cells considered as a potential source for sufficient amounts of donor material. Adequate preclinical models representing retinal disease conditions of potential future patients are needed for translation research. Here we compared transplant integration in mouse models with mild (prominin1-deficient; Prom1-/-) or severe (cone photoreceptor function loss 1/rhodopsin-deficient double-mutant; Cpfl1/Rho-/-) cone-rod degeneration.

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