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BMP-induced reprogramming of the neural retina into retinal pigment epithelium requires Wnt signalling

Steinfeld, Jörg ; Steinfeld, Ichie ; Bausch, Alexander ; Coronato, Nicola ; Hampel, Meggi-Lee ; Depner, Heike ; Layer, Paul G. ; Vogel-Höpker, A. (2017)
BMP-induced reprogramming of the neural retina into retinal pigment epithelium requires Wnt signalling.
In: Biology open, 6 (7)
Article, Bibliographie

Abstract

In vertebrates, the retinal pigment epithelium (RPE) and photoreceptors of the neural retina (NR) comprise a functional unit required for vision. During vertebrate eye development, a conversion of the RPE into NR can be induced by growth factors in vivo at optic cup stages, but the reverse process, the conversion of NR tissue into RPE has not been reported. Here, we show that bone morphogenetic proteins (BMP) signalling can reprogram the NR into RPE at optic cup stages in chick. Shortly after BMP application, expression of Microphthalmia associated transcription factor (Mitf) is induced in the NR and selective cell death on the basal side of the NR induces an RPE-like morphology. The newly induced RPE differentiates and expresses Melanosomalmatrix protein 115 (Mmp115) and RPE65. BMP-induced Wnt2b expression is observed in regions of the NR that become pigmented. Loss of function studies show that conversion of the NR into RPE requires both BMP and WNT signalling. Simultanousely to the appearance of ectopic RPE tissue, BMP application induced ectopic retinal tissue in the proximal RPE of the chick optic cup. The newly induced NR is multi-layered and expresses the Visual segment homeobox-containing gene (Vsx2) and the ganglion- and photoreceptor cell markers Brn3α and Visinin are detected. Our results show that high BMP concentrations are required to induce the conversion of NR into RPE, while low BMP concentrations can still induce transdifferentiation of the RPE into NR. This knowledge may contribute to the development of efficient standardized protocols for RPE- and NR generation for cell replacement therapies.

Item Type: Article
Erschienen: 2017
Creators: Steinfeld, Jörg ; Steinfeld, Ichie ; Bausch, Alexander ; Coronato, Nicola ; Hampel, Meggi-Lee ; Depner, Heike ; Layer, Paul G. ; Vogel-Höpker, A.
Type of entry: Bibliographie
Title: BMP-induced reprogramming of the neural retina into retinal pigment epithelium requires Wnt signalling
Language: English
Date: 15 July 2017
Journal or Publication Title: Biology open
Volume of the journal: 6
Issue Number: 7
Abstract:

In vertebrates, the retinal pigment epithelium (RPE) and photoreceptors of the neural retina (NR) comprise a functional unit required for vision. During vertebrate eye development, a conversion of the RPE into NR can be induced by growth factors in vivo at optic cup stages, but the reverse process, the conversion of NR tissue into RPE has not been reported. Here, we show that bone morphogenetic proteins (BMP) signalling can reprogram the NR into RPE at optic cup stages in chick. Shortly after BMP application, expression of Microphthalmia associated transcription factor (Mitf) is induced in the NR and selective cell death on the basal side of the NR induces an RPE-like morphology. The newly induced RPE differentiates and expresses Melanosomalmatrix protein 115 (Mmp115) and RPE65. BMP-induced Wnt2b expression is observed in regions of the NR that become pigmented. Loss of function studies show that conversion of the NR into RPE requires both BMP and WNT signalling. Simultanousely to the appearance of ectopic RPE tissue, BMP application induced ectopic retinal tissue in the proximal RPE of the chick optic cup. The newly induced NR is multi-layered and expresses the Visual segment homeobox-containing gene (Vsx2) and the ganglion- and photoreceptor cell markers Brn3α and Visinin are detected. Our results show that high BMP concentrations are required to induce the conversion of NR into RPE, while low BMP concentrations can still induce transdifferentiation of the RPE into NR. This knowledge may contribute to the development of efficient standardized protocols for RPE- and NR generation for cell replacement therapies.

Identification Number: pmid:28546339
Divisions: 10 Department of Biology
10 Department of Biology > Regulation of Early Eye Development
10 Department of Biology > Developmental Biology and Neurogenetics
Date Deposited: 30 May 2017 07:10
Last Modified: 27 Sep 2017 12:20
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