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A Novel Therapeutic Target in Inflammatory Uveitis: Transglutaminase 2 Inhibitor

PURPOSE: Our goal was to investigate the effects of inhibition of transglutaminase 2 (TGase 2) on endotoxin-induced uveitis (EIU) METHODS: EIU was induced in female Lewis rats by single footpad injections of 200 µg of lipopolysaccharide (LPS). TGase 2 inhibitors were administered intraperitoneally 3...

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Autores principales: Sohn, Joonhong, Chae, Ju Byung, Lee, Sun Young, Kim, Soo-Youl, Kim, June-Gone
Formato: Texto
Lenguaje:English
Publicado: The Korean Ophthalmological Society 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2817820/
https://www.ncbi.nlm.nih.gov/pubmed/20157411
http://dx.doi.org/10.3341/kjo.2010.24.1.29
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author Sohn, Joonhong
Chae, Ju Byung
Lee, Sun Young
Kim, Soo-Youl
Kim, June-Gone
author_facet Sohn, Joonhong
Chae, Ju Byung
Lee, Sun Young
Kim, Soo-Youl
Kim, June-Gone
author_sort Sohn, Joonhong
collection PubMed
description PURPOSE: Our goal was to investigate the effects of inhibition of transglutaminase 2 (TGase 2) on endotoxin-induced uveitis (EIU) METHODS: EIU was induced in female Lewis rats by single footpad injections of 200 µg of lipopolysaccharide (LPS). TGase 2 inhibitors were administered intraperitoneally 30 minutes before and at the time of LPS administration. Rats were sacrificed 24 hours after injection, and the effects of the TGase 2 inhibitors were evaluated by the number of intraocular inflammatory cells present on histologic sections and by measuring the TGase 2 activity and TGase products in the aqueous humor (AqH). TGase 2 substrates were also assayed in AqH from uveitis patients. RESULTS: Clinical indications of EIU, the number of cells present on histologic sections, and TGase 2 activity in AqH increased in a time-dependent manner, peaking 24 hours after LPS injection. Inflammation in EIU was significantly reversed by treatment with TGase inhibitors. A 23-kDa cross-linked TGase substrate was identified in the AqH from EIU rats and uveitis patients. MALDI-TOF analysis showed that this substrate in uveitis patients was human Ig kappa chain C region. CONCLUSIONS: TGase 2 activity and its catalytic product were increased in the AqH of EIU rats. TGase 2 inhibition attenuated the degree of inflammation in EIU. Safe and stable TGase inhibitors may have great potential for the treatment of inflammatory uveitis.
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spelling pubmed-28178202010-02-12 A Novel Therapeutic Target in Inflammatory Uveitis: Transglutaminase 2 Inhibitor Sohn, Joonhong Chae, Ju Byung Lee, Sun Young Kim, Soo-Youl Kim, June-Gone Korean J Ophthalmol Original Article PURPOSE: Our goal was to investigate the effects of inhibition of transglutaminase 2 (TGase 2) on endotoxin-induced uveitis (EIU) METHODS: EIU was induced in female Lewis rats by single footpad injections of 200 µg of lipopolysaccharide (LPS). TGase 2 inhibitors were administered intraperitoneally 30 minutes before and at the time of LPS administration. Rats were sacrificed 24 hours after injection, and the effects of the TGase 2 inhibitors were evaluated by the number of intraocular inflammatory cells present on histologic sections and by measuring the TGase 2 activity and TGase products in the aqueous humor (AqH). TGase 2 substrates were also assayed in AqH from uveitis patients. RESULTS: Clinical indications of EIU, the number of cells present on histologic sections, and TGase 2 activity in AqH increased in a time-dependent manner, peaking 24 hours after LPS injection. Inflammation in EIU was significantly reversed by treatment with TGase inhibitors. A 23-kDa cross-linked TGase substrate was identified in the AqH from EIU rats and uveitis patients. MALDI-TOF analysis showed that this substrate in uveitis patients was human Ig kappa chain C region. CONCLUSIONS: TGase 2 activity and its catalytic product were increased in the AqH of EIU rats. TGase 2 inhibition attenuated the degree of inflammation in EIU. Safe and stable TGase inhibitors may have great potential for the treatment of inflammatory uveitis. The Korean Ophthalmological Society 2010-02 2010-02-05 /pmc/articles/PMC2817820/ /pubmed/20157411 http://dx.doi.org/10.3341/kjo.2010.24.1.29 Text en © 2010 The Korean Ophthalmological Society http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Sohn, Joonhong
Chae, Ju Byung
Lee, Sun Young
Kim, Soo-Youl
Kim, June-Gone
A Novel Therapeutic Target in Inflammatory Uveitis: Transglutaminase 2 Inhibitor
title A Novel Therapeutic Target in Inflammatory Uveitis: Transglutaminase 2 Inhibitor
title_full A Novel Therapeutic Target in Inflammatory Uveitis: Transglutaminase 2 Inhibitor
title_fullStr A Novel Therapeutic Target in Inflammatory Uveitis: Transglutaminase 2 Inhibitor
title_full_unstemmed A Novel Therapeutic Target in Inflammatory Uveitis: Transglutaminase 2 Inhibitor
title_short A Novel Therapeutic Target in Inflammatory Uveitis: Transglutaminase 2 Inhibitor
title_sort novel therapeutic target in inflammatory uveitis: transglutaminase 2 inhibitor
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2817820/
https://www.ncbi.nlm.nih.gov/pubmed/20157411
http://dx.doi.org/10.3341/kjo.2010.24.1.29
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