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Transcriptional Profiling Identifies Upregulation of Neuroprotective Pathways in Retinitis Pigmentosa
Hereditary retinal degenerations like retinitis pigmentosa (RP) are among the leading causes of blindness in younger patients. To enable in vivo investigation of cellular and molecular mechanisms responsible for photoreceptor cell death and to allow testing of therapeutic strategies that could preve...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8231189/ https://www.ncbi.nlm.nih.gov/pubmed/34208383 http://dx.doi.org/10.3390/ijms22126307 |
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author | Bielmeier, Christina B. Roth, Saskia Schmitt, Sabrina I. Boneva, Stefaniya K. Schlecht, Anja Vallon, Mario Tamm, Ernst R. Ergün, Süleyman Neueder, Andreas Braunger, Barbara M. |
author_facet | Bielmeier, Christina B. Roth, Saskia Schmitt, Sabrina I. Boneva, Stefaniya K. Schlecht, Anja Vallon, Mario Tamm, Ernst R. Ergün, Süleyman Neueder, Andreas Braunger, Barbara M. |
author_sort | Bielmeier, Christina B. |
collection | PubMed |
description | Hereditary retinal degenerations like retinitis pigmentosa (RP) are among the leading causes of blindness in younger patients. To enable in vivo investigation of cellular and molecular mechanisms responsible for photoreceptor cell death and to allow testing of therapeutic strategies that could prevent retinal degeneration, animal models have been created. In this study, we deeply characterized the transcriptional profile of mice carrying the transgene rhodopsin V20G/P23H/P27L (VPP), which is a model for autosomal dominant RP. We examined the degree of photoreceptor degeneration and studied the impact of the VPP transgene-induced retinal degeneration on the transcriptome level of the retina using next generation RNA sequencing (RNASeq) analyses followed by weighted correlation network analysis (WGCNA). We furthermore identified cellular subpopulations responsible for some of the observed dysregulations using in situ hybridizations, immunofluorescence staining, and 3D reconstruction. Using RNASeq analysis, we identified 9256 dysregulated genes and six significantly associated gene modules in the subsequently performed WGCNA. Gene ontology enrichment showed, among others, dysregulation of genes involved in TGF-β regulated extracellular matrix organization, the (ocular) immune system/response, and cellular homeostasis. Moreover, heatmaps confirmed clustering of significantly dysregulated genes coding for components of the TGF-β, G-protein activated, and VEGF signaling pathway. 3D reconstructions of immunostained/in situ hybridized sections revealed retinal neurons and Müller cells as the major cellular population expressing representative components of these signaling pathways. The predominant effect of VPP-induced photoreceptor degeneration pointed towards induction of neuroinflammation and the upregulation of neuroprotective pathways like TGF-β, G-protein activated, and VEGF signaling. Thus, modulation of these processes and signaling pathways might represent new therapeutic options to delay the degeneration of photoreceptors in diseases like RP. |
format | Online Article Text |
id | pubmed-8231189 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-82311892021-06-26 Transcriptional Profiling Identifies Upregulation of Neuroprotective Pathways in Retinitis Pigmentosa Bielmeier, Christina B. Roth, Saskia Schmitt, Sabrina I. Boneva, Stefaniya K. Schlecht, Anja Vallon, Mario Tamm, Ernst R. Ergün, Süleyman Neueder, Andreas Braunger, Barbara M. Int J Mol Sci Article Hereditary retinal degenerations like retinitis pigmentosa (RP) are among the leading causes of blindness in younger patients. To enable in vivo investigation of cellular and molecular mechanisms responsible for photoreceptor cell death and to allow testing of therapeutic strategies that could prevent retinal degeneration, animal models have been created. In this study, we deeply characterized the transcriptional profile of mice carrying the transgene rhodopsin V20G/P23H/P27L (VPP), which is a model for autosomal dominant RP. We examined the degree of photoreceptor degeneration and studied the impact of the VPP transgene-induced retinal degeneration on the transcriptome level of the retina using next generation RNA sequencing (RNASeq) analyses followed by weighted correlation network analysis (WGCNA). We furthermore identified cellular subpopulations responsible for some of the observed dysregulations using in situ hybridizations, immunofluorescence staining, and 3D reconstruction. Using RNASeq analysis, we identified 9256 dysregulated genes and six significantly associated gene modules in the subsequently performed WGCNA. Gene ontology enrichment showed, among others, dysregulation of genes involved in TGF-β regulated extracellular matrix organization, the (ocular) immune system/response, and cellular homeostasis. Moreover, heatmaps confirmed clustering of significantly dysregulated genes coding for components of the TGF-β, G-protein activated, and VEGF signaling pathway. 3D reconstructions of immunostained/in situ hybridized sections revealed retinal neurons and Müller cells as the major cellular population expressing representative components of these signaling pathways. The predominant effect of VPP-induced photoreceptor degeneration pointed towards induction of neuroinflammation and the upregulation of neuroprotective pathways like TGF-β, G-protein activated, and VEGF signaling. Thus, modulation of these processes and signaling pathways might represent new therapeutic options to delay the degeneration of photoreceptors in diseases like RP. MDPI 2021-06-11 /pmc/articles/PMC8231189/ /pubmed/34208383 http://dx.doi.org/10.3390/ijms22126307 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Bielmeier, Christina B. Roth, Saskia Schmitt, Sabrina I. Boneva, Stefaniya K. Schlecht, Anja Vallon, Mario Tamm, Ernst R. Ergün, Süleyman Neueder, Andreas Braunger, Barbara M. Transcriptional Profiling Identifies Upregulation of Neuroprotective Pathways in Retinitis Pigmentosa |
title | Transcriptional Profiling Identifies Upregulation of Neuroprotective Pathways in Retinitis Pigmentosa |
title_full | Transcriptional Profiling Identifies Upregulation of Neuroprotective Pathways in Retinitis Pigmentosa |
title_fullStr | Transcriptional Profiling Identifies Upregulation of Neuroprotective Pathways in Retinitis Pigmentosa |
title_full_unstemmed | Transcriptional Profiling Identifies Upregulation of Neuroprotective Pathways in Retinitis Pigmentosa |
title_short | Transcriptional Profiling Identifies Upregulation of Neuroprotective Pathways in Retinitis Pigmentosa |
title_sort | transcriptional profiling identifies upregulation of neuroprotective pathways in retinitis pigmentosa |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8231189/ https://www.ncbi.nlm.nih.gov/pubmed/34208383 http://dx.doi.org/10.3390/ijms22126307 |
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