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Transduced Tat-CIAPIN1 reduces the inflammatory response on LPS− and TPA-induced damages
Cytokine-induced apoptosis inhibitor 1 (CIAPIN1), known as an anti-apoptotic and signal-transduction protein, plays a pivotal role in a variety of biological processes. However, the role of CIAPIN1 in inflammation is unclear. We investigated the protective effects of CIAPIN1 in lipopolysaccharide (L...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society for Biochemistry and Molecular Biology
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6941760/ https://www.ncbi.nlm.nih.gov/pubmed/31722779 http://dx.doi.org/10.5483/BMBRep.2019.52.12.245 |
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author | Yeo, Hyeon Ji Shin, Min Jea You, Ji Ho Kim, Jeong Su Kim, Min Young Kim, Dae Won Kim, Duk-Soo Eum, Won Sik Choi, Soo Young |
author_facet | Yeo, Hyeon Ji Shin, Min Jea You, Ji Ho Kim, Jeong Su Kim, Min Young Kim, Dae Won Kim, Duk-Soo Eum, Won Sik Choi, Soo Young |
author_sort | Yeo, Hyeon Ji |
collection | PubMed |
description | Cytokine-induced apoptosis inhibitor 1 (CIAPIN1), known as an anti-apoptotic and signal-transduction protein, plays a pivotal role in a variety of biological processes. However, the role of CIAPIN1 in inflammation is unclear. We investigated the protective effects of CIAPIN1 in lipopolysaccharide (LPS)-exposed Raw 264.7 cells and against inflammatory damage induced by 12-O-tetradecanoylphorbol-13-acetate (TPA) in a mouse model using cell-permeable Tat-CIAPIN1. Transduced Tat-CIAPIN1 significantly reduced ROS production and DNA fragmentation in LPS-exposed Raw 264.7 cells. Also, Tat-CIAPIN1 inhibited MAPKs and NF-κB activation, reduced the expression of Bax, and cleaved caspase-3, COX-2, iNOS, IL-6, and TNF-α in LPS-exposed cells. In a TPA-induced animal model, transduced Tat-CIAPIN1 drastically decreased inflammation damage and inhibited COX-2, iNOS, IL-6, and TNF-α expression. Therefore, these findings suggest that Tat-CIAPIN1 might lead to a new strategy for the treatment of inflammatory skin disorders. |
format | Online Article Text |
id | pubmed-6941760 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Korean Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-69417602020-01-08 Transduced Tat-CIAPIN1 reduces the inflammatory response on LPS− and TPA-induced damages Yeo, Hyeon Ji Shin, Min Jea You, Ji Ho Kim, Jeong Su Kim, Min Young Kim, Dae Won Kim, Duk-Soo Eum, Won Sik Choi, Soo Young BMB Rep Articles Cytokine-induced apoptosis inhibitor 1 (CIAPIN1), known as an anti-apoptotic and signal-transduction protein, plays a pivotal role in a variety of biological processes. However, the role of CIAPIN1 in inflammation is unclear. We investigated the protective effects of CIAPIN1 in lipopolysaccharide (LPS)-exposed Raw 264.7 cells and against inflammatory damage induced by 12-O-tetradecanoylphorbol-13-acetate (TPA) in a mouse model using cell-permeable Tat-CIAPIN1. Transduced Tat-CIAPIN1 significantly reduced ROS production and DNA fragmentation in LPS-exposed Raw 264.7 cells. Also, Tat-CIAPIN1 inhibited MAPKs and NF-κB activation, reduced the expression of Bax, and cleaved caspase-3, COX-2, iNOS, IL-6, and TNF-α in LPS-exposed cells. In a TPA-induced animal model, transduced Tat-CIAPIN1 drastically decreased inflammation damage and inhibited COX-2, iNOS, IL-6, and TNF-α expression. Therefore, these findings suggest that Tat-CIAPIN1 might lead to a new strategy for the treatment of inflammatory skin disorders. Korean Society for Biochemistry and Molecular Biology 2019-12 2019-12-31 /pmc/articles/PMC6941760/ /pubmed/31722779 http://dx.doi.org/10.5483/BMBRep.2019.52.12.245 Text en Copyright © 2019 by the The Korean Society for Biochemistry and Molecular Biology This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Yeo, Hyeon Ji Shin, Min Jea You, Ji Ho Kim, Jeong Su Kim, Min Young Kim, Dae Won Kim, Duk-Soo Eum, Won Sik Choi, Soo Young Transduced Tat-CIAPIN1 reduces the inflammatory response on LPS− and TPA-induced damages |
title | Transduced Tat-CIAPIN1 reduces the inflammatory response on LPS− and TPA-induced damages |
title_full | Transduced Tat-CIAPIN1 reduces the inflammatory response on LPS− and TPA-induced damages |
title_fullStr | Transduced Tat-CIAPIN1 reduces the inflammatory response on LPS− and TPA-induced damages |
title_full_unstemmed | Transduced Tat-CIAPIN1 reduces the inflammatory response on LPS− and TPA-induced damages |
title_short | Transduced Tat-CIAPIN1 reduces the inflammatory response on LPS− and TPA-induced damages |
title_sort | transduced tat-ciapin1 reduces the inflammatory response on lps− and tpa-induced damages |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6941760/ https://www.ncbi.nlm.nih.gov/pubmed/31722779 http://dx.doi.org/10.5483/BMBRep.2019.52.12.245 |
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