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Unilateral acute anterior uveitis is associated with ipsilateral changes in the tear fluid proteome that involves the LXR/RXR pathway
PURPOSE: To determine whether unilateral acute anterior uveitis (AAU) induces ipsilateral changes in the tear fluid proteome. METHODS: Five patients (25–77 years old) with unilateral AAU were included. Tear fluid samples were obtained using Schirmer’s test strips. The healthy eye served as control....
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7250997/ https://www.ncbi.nlm.nih.gov/pubmed/32458144 http://dx.doi.org/10.1186/s12348-020-00204-4 |
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author | Eidet, Jon Roger Jørstad, Øystein Kalsnes Fostad, Ida G. Olstad, Ole K. Sørland, Ragnhild Ø. Moe, Morten C. Petrovski, Goran Pepaj, Milaim |
author_facet | Eidet, Jon Roger Jørstad, Øystein Kalsnes Fostad, Ida G. Olstad, Ole K. Sørland, Ragnhild Ø. Moe, Morten C. Petrovski, Goran Pepaj, Milaim |
author_sort | Eidet, Jon Roger |
collection | PubMed |
description | PURPOSE: To determine whether unilateral acute anterior uveitis (AAU) induces ipsilateral changes in the tear fluid proteome. METHODS: Five patients (25–77 years old) with unilateral AAU were included. Tear fluid samples were obtained using Schirmer’s test strips. The healthy eye served as control. Proteins were identified by liquid chromatography tandem mass spectrometry. RESULTS: Two hundred forty-two tear fluid sample proteins were identified, of which 75 were present in at least three patients. Nine proteins were at least 1.5-fold increased, whereas eight were at least 1.5-fold decreased in tears from the diseased eye compared with the healthy eye. APOBEC3A was significantly increased (1.43-fold; P = 0.04), whereas TGM2 was significantly decreased (− 1.21-fold; P = 0.03) in tears from the diseased eye relative to the healthy eye. Ingenuity Pathway Analysis identified LXR/RXR (P < 1.02E−4) as a top canonical pathway. CONCLUSION: Unilateral AAU induced detectable changes in the ipsilateral tear fluid proteome and involvement of the inflammation-associated LXR/RXR pathway. |
format | Online Article Text |
id | pubmed-7250997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-72509972020-06-05 Unilateral acute anterior uveitis is associated with ipsilateral changes in the tear fluid proteome that involves the LXR/RXR pathway Eidet, Jon Roger Jørstad, Øystein Kalsnes Fostad, Ida G. Olstad, Ole K. Sørland, Ragnhild Ø. Moe, Morten C. Petrovski, Goran Pepaj, Milaim J Ophthalmic Inflamm Infect Brief Report PURPOSE: To determine whether unilateral acute anterior uveitis (AAU) induces ipsilateral changes in the tear fluid proteome. METHODS: Five patients (25–77 years old) with unilateral AAU were included. Tear fluid samples were obtained using Schirmer’s test strips. The healthy eye served as control. Proteins were identified by liquid chromatography tandem mass spectrometry. RESULTS: Two hundred forty-two tear fluid sample proteins were identified, of which 75 were present in at least three patients. Nine proteins were at least 1.5-fold increased, whereas eight were at least 1.5-fold decreased in tears from the diseased eye compared with the healthy eye. APOBEC3A was significantly increased (1.43-fold; P = 0.04), whereas TGM2 was significantly decreased (− 1.21-fold; P = 0.03) in tears from the diseased eye relative to the healthy eye. Ingenuity Pathway Analysis identified LXR/RXR (P < 1.02E−4) as a top canonical pathway. CONCLUSION: Unilateral AAU induced detectable changes in the ipsilateral tear fluid proteome and involvement of the inflammation-associated LXR/RXR pathway. Springer Berlin Heidelberg 2020-05-27 /pmc/articles/PMC7250997/ /pubmed/32458144 http://dx.doi.org/10.1186/s12348-020-00204-4 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Brief Report Eidet, Jon Roger Jørstad, Øystein Kalsnes Fostad, Ida G. Olstad, Ole K. Sørland, Ragnhild Ø. Moe, Morten C. Petrovski, Goran Pepaj, Milaim Unilateral acute anterior uveitis is associated with ipsilateral changes in the tear fluid proteome that involves the LXR/RXR pathway |
title | Unilateral acute anterior uveitis is associated with ipsilateral changes in the tear fluid proteome that involves the LXR/RXR pathway |
title_full | Unilateral acute anterior uveitis is associated with ipsilateral changes in the tear fluid proteome that involves the LXR/RXR pathway |
title_fullStr | Unilateral acute anterior uveitis is associated with ipsilateral changes in the tear fluid proteome that involves the LXR/RXR pathway |
title_full_unstemmed | Unilateral acute anterior uveitis is associated with ipsilateral changes in the tear fluid proteome that involves the LXR/RXR pathway |
title_short | Unilateral acute anterior uveitis is associated with ipsilateral changes in the tear fluid proteome that involves the LXR/RXR pathway |
title_sort | unilateral acute anterior uveitis is associated with ipsilateral changes in the tear fluid proteome that involves the lxr/rxr pathway |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7250997/ https://www.ncbi.nlm.nih.gov/pubmed/32458144 http://dx.doi.org/10.1186/s12348-020-00204-4 |
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