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miRNA Changes in Retinal Ganglion Cells after Optic Nerve Crush and Glaucomatous Damage
The purpose of this study was to characterize the miRNA profile of purified retinal ganglion cells (RGC) from healthy and diseased rat retina. Diseased retina includes those after a traumatic optic nerve crush (ONC), and after ocular hypertension/glaucoma. Rats were separated into four groups: healt...
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/PMC8305746/ https://www.ncbi.nlm.nih.gov/pubmed/34206213 http://dx.doi.org/10.3390/cells10071564 |
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author | Mead, Ben Kerr, Alicia Nakaya, Naoki Tomarev, Stanislav I. |
author_facet | Mead, Ben Kerr, Alicia Nakaya, Naoki Tomarev, Stanislav I. |
author_sort | Mead, Ben |
collection | PubMed |
description | The purpose of this study was to characterize the miRNA profile of purified retinal ganglion cells (RGC) from healthy and diseased rat retina. Diseased retina includes those after a traumatic optic nerve crush (ONC), and after ocular hypertension/glaucoma. Rats were separated into four groups: healthy/intact, 7 days after laser-induced ocular hypertension, 2 days after traumatic ONC, and 7 days after ONC. RGC were purified from rat retina using microbeads conjugated to CD90.1/Thy1. RNA were sequenced using Next Generation Sequencing. Over 100 miRNA were identified that were significantly different in diseased retina compared to healthy retina. Considerable differences were seen in the miRNA expression of RGC 7 days after ONC, whereas after 2 days, few changes were seen. The miRNA profiles of RGC 7 days after ONC and 7 days after ocular hypertension were similar, but discrete miRNA differences were still seen. Candidate mRNA showing different levels of expression after retinal injury were manipulated in RGC cultures using mimics/AntagomiRs. Of the five candidate miRNA identified and subsequently tested for therapeutic efficacy, miR-194 inhibitor and miR-664-2 inhibitor elicited significant RGC neuroprotection, whereas miR-181a mimic and miR-181d-5p mimic elicited significant RGC neuritogenesis. |
format | Online Article Text |
id | pubmed-8305746 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83057462021-07-25 miRNA Changes in Retinal Ganglion Cells after Optic Nerve Crush and Glaucomatous Damage Mead, Ben Kerr, Alicia Nakaya, Naoki Tomarev, Stanislav I. Cells Article The purpose of this study was to characterize the miRNA profile of purified retinal ganglion cells (RGC) from healthy and diseased rat retina. Diseased retina includes those after a traumatic optic nerve crush (ONC), and after ocular hypertension/glaucoma. Rats were separated into four groups: healthy/intact, 7 days after laser-induced ocular hypertension, 2 days after traumatic ONC, and 7 days after ONC. RGC were purified from rat retina using microbeads conjugated to CD90.1/Thy1. RNA were sequenced using Next Generation Sequencing. Over 100 miRNA were identified that were significantly different in diseased retina compared to healthy retina. Considerable differences were seen in the miRNA expression of RGC 7 days after ONC, whereas after 2 days, few changes were seen. The miRNA profiles of RGC 7 days after ONC and 7 days after ocular hypertension were similar, but discrete miRNA differences were still seen. Candidate mRNA showing different levels of expression after retinal injury were manipulated in RGC cultures using mimics/AntagomiRs. Of the five candidate miRNA identified and subsequently tested for therapeutic efficacy, miR-194 inhibitor and miR-664-2 inhibitor elicited significant RGC neuroprotection, whereas miR-181a mimic and miR-181d-5p mimic elicited significant RGC neuritogenesis. MDPI 2021-06-22 /pmc/articles/PMC8305746/ /pubmed/34206213 http://dx.doi.org/10.3390/cells10071564 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 Mead, Ben Kerr, Alicia Nakaya, Naoki Tomarev, Stanislav I. miRNA Changes in Retinal Ganglion Cells after Optic Nerve Crush and Glaucomatous Damage |
title | miRNA Changes in Retinal Ganglion Cells after Optic Nerve Crush and Glaucomatous Damage |
title_full | miRNA Changes in Retinal Ganglion Cells after Optic Nerve Crush and Glaucomatous Damage |
title_fullStr | miRNA Changes in Retinal Ganglion Cells after Optic Nerve Crush and Glaucomatous Damage |
title_full_unstemmed | miRNA Changes in Retinal Ganglion Cells after Optic Nerve Crush and Glaucomatous Damage |
title_short | miRNA Changes in Retinal Ganglion Cells after Optic Nerve Crush and Glaucomatous Damage |
title_sort | mirna changes in retinal ganglion cells after optic nerve crush and glaucomatous damage |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8305746/ https://www.ncbi.nlm.nih.gov/pubmed/34206213 http://dx.doi.org/10.3390/cells10071564 |
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