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Candidate proteins from predegenerated nerve exert time-specific protection of retinal ganglion cells in glaucoma
Glaucoma is thought to be the main cause of severe visual impairment or permanent loss of vision. Current therapeutic strategies are not sufficient to protect against glaucoma. Thus, new therapies and potential novel therapeutic targets must be developed to achieve progress in the treatment of this...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5673995/ https://www.ncbi.nlm.nih.gov/pubmed/29109409 http://dx.doi.org/10.1038/s41598-017-14860-5 |
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author | Pietrucha-Dutczak, Marita Smedowski, Adrian Liu, Xiaonan Matuszek, Iwona Varjosalo, Markku Lewin-Kowalik, Joanna |
author_facet | Pietrucha-Dutczak, Marita Smedowski, Adrian Liu, Xiaonan Matuszek, Iwona Varjosalo, Markku Lewin-Kowalik, Joanna |
author_sort | Pietrucha-Dutczak, Marita |
collection | PubMed |
description | Glaucoma is thought to be the main cause of severe visual impairment or permanent loss of vision. Current therapeutic strategies are not sufficient to protect against glaucoma. Thus, new therapies and potential novel therapeutic targets must be developed to achieve progress in the treatment of this insidious disease. This study was undertaken to verify whether the time of administration of an extract from predegenerated rat sciatic nerves as well as exposure time of this extract onto retinal ganglion cells (RGCs) influences the survival of RGCs in a rat glaucoma model. We have demonstrated that extract obtained from the predegenerated sciatic nerves protects RGCs in a rat glaucoma model. The neuroprotective effect depends mostly on the time of administration of the extract and less clearly on the time of exposure to the extract and is associated with stimulation of endogenous BDNF expression both in RGCs and glial cells. The 14(th) day following glaucoma induction represents a therapeutic window for effective treatment in a glaucoma model. Mass Spectrometry analysis demonstrated that metallothionein 2 (MT2) may be a key molecule responsible for neuroprotective effects on RGC survival. |
format | Online Article Text |
id | pubmed-5673995 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56739952017-11-15 Candidate proteins from predegenerated nerve exert time-specific protection of retinal ganglion cells in glaucoma Pietrucha-Dutczak, Marita Smedowski, Adrian Liu, Xiaonan Matuszek, Iwona Varjosalo, Markku Lewin-Kowalik, Joanna Sci Rep Article Glaucoma is thought to be the main cause of severe visual impairment or permanent loss of vision. Current therapeutic strategies are not sufficient to protect against glaucoma. Thus, new therapies and potential novel therapeutic targets must be developed to achieve progress in the treatment of this insidious disease. This study was undertaken to verify whether the time of administration of an extract from predegenerated rat sciatic nerves as well as exposure time of this extract onto retinal ganglion cells (RGCs) influences the survival of RGCs in a rat glaucoma model. We have demonstrated that extract obtained from the predegenerated sciatic nerves protects RGCs in a rat glaucoma model. The neuroprotective effect depends mostly on the time of administration of the extract and less clearly on the time of exposure to the extract and is associated with stimulation of endogenous BDNF expression both in RGCs and glial cells. The 14(th) day following glaucoma induction represents a therapeutic window for effective treatment in a glaucoma model. Mass Spectrometry analysis demonstrated that metallothionein 2 (MT2) may be a key molecule responsible for neuroprotective effects on RGC survival. Nature Publishing Group UK 2017-11-06 /pmc/articles/PMC5673995/ /pubmed/29109409 http://dx.doi.org/10.1038/s41598-017-14860-5 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Pietrucha-Dutczak, Marita Smedowski, Adrian Liu, Xiaonan Matuszek, Iwona Varjosalo, Markku Lewin-Kowalik, Joanna Candidate proteins from predegenerated nerve exert time-specific protection of retinal ganglion cells in glaucoma |
title | Candidate proteins from predegenerated nerve exert time-specific protection of retinal ganglion cells in glaucoma |
title_full | Candidate proteins from predegenerated nerve exert time-specific protection of retinal ganglion cells in glaucoma |
title_fullStr | Candidate proteins from predegenerated nerve exert time-specific protection of retinal ganglion cells in glaucoma |
title_full_unstemmed | Candidate proteins from predegenerated nerve exert time-specific protection of retinal ganglion cells in glaucoma |
title_short | Candidate proteins from predegenerated nerve exert time-specific protection of retinal ganglion cells in glaucoma |
title_sort | candidate proteins from predegenerated nerve exert time-specific protection of retinal ganglion cells in glaucoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5673995/ https://www.ncbi.nlm.nih.gov/pubmed/29109409 http://dx.doi.org/10.1038/s41598-017-14860-5 |
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