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Compensation of cATSCs-derived TGFβ1 and IL10 expressions was effectively modulated atopic dermatitis

In this study, we found an effective and novel therapeutic approach to atopic dermatitis (AD) therapy via treatment with a canine adipose tissue stem cell (cATSC) extract. We determined that the therapeutic application of cATSC-derived interleukin 10 (IL10) and transforming growth factor β1 (TGFβ1)...

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Autores principales: Jee, M K, Im, Y B, Choi, J I, Kang, S K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3734835/
https://www.ncbi.nlm.nih.gov/pubmed/23412382
http://dx.doi.org/10.1038/cddis.2013.4
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author Jee, M K
Im, Y B
Choi, J I
Kang, S K
author_facet Jee, M K
Im, Y B
Choi, J I
Kang, S K
author_sort Jee, M K
collection PubMed
description In this study, we found an effective and novel therapeutic approach to atopic dermatitis (AD) therapy via treatment with a canine adipose tissue stem cell (cATSC) extract. We determined that the therapeutic application of cATSC-derived interleukin 10 (IL10) and transforming growth factor β1 (TGFβ1) effectively modulated the overloaded immune response after the induction of AD. In addition, we investigated the molecular role of the cATSC extract during AD treatment. Dogs with naturally occurring AD that was treated at Seoul National University Veterinary Teaching Hospital was enrolled in this study. Owner consent was obtained for privately owned dogs before enrollment. We prepared a primary fat-derived cATSC extract that contained various functional factors, including IL10 and TGFβ1, as a treatment for AD. We found that the cATSC extract significantly ameliorated the pathological symptoms of canine AD. The cATSC extract secreted the immunomodulatory cytokines IL10 and TGFβ1, which modulated the overloaded immune response after the induction of AD. Moreover, these immunomodulatory cytokines modulated AD-induced inflammation and inactivated the pathological signals IL6, INFγ, iNOS, eNOS and Nox4. Additionally, these cytokines protected against apoptotic keratinocyte degeneration. This study demonstrated the novel therapeutic efficacy of the cATSC extract during successive AD treatments, which suggests a potential therapeutic use for human AD patients.
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spelling pubmed-37348352013-08-06 Compensation of cATSCs-derived TGFβ1 and IL10 expressions was effectively modulated atopic dermatitis Jee, M K Im, Y B Choi, J I Kang, S K Cell Death Dis Original Article In this study, we found an effective and novel therapeutic approach to atopic dermatitis (AD) therapy via treatment with a canine adipose tissue stem cell (cATSC) extract. We determined that the therapeutic application of cATSC-derived interleukin 10 (IL10) and transforming growth factor β1 (TGFβ1) effectively modulated the overloaded immune response after the induction of AD. In addition, we investigated the molecular role of the cATSC extract during AD treatment. Dogs with naturally occurring AD that was treated at Seoul National University Veterinary Teaching Hospital was enrolled in this study. Owner consent was obtained for privately owned dogs before enrollment. We prepared a primary fat-derived cATSC extract that contained various functional factors, including IL10 and TGFβ1, as a treatment for AD. We found that the cATSC extract significantly ameliorated the pathological symptoms of canine AD. The cATSC extract secreted the immunomodulatory cytokines IL10 and TGFβ1, which modulated the overloaded immune response after the induction of AD. Moreover, these immunomodulatory cytokines modulated AD-induced inflammation and inactivated the pathological signals IL6, INFγ, iNOS, eNOS and Nox4. Additionally, these cytokines protected against apoptotic keratinocyte degeneration. This study demonstrated the novel therapeutic efficacy of the cATSC extract during successive AD treatments, which suggests a potential therapeutic use for human AD patients. Nature Publishing Group 2013-02 2013-02-14 /pmc/articles/PMC3734835/ /pubmed/23412382 http://dx.doi.org/10.1038/cddis.2013.4 Text en Copyright © 2013 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Original Article
Jee, M K
Im, Y B
Choi, J I
Kang, S K
Compensation of cATSCs-derived TGFβ1 and IL10 expressions was effectively modulated atopic dermatitis
title Compensation of cATSCs-derived TGFβ1 and IL10 expressions was effectively modulated atopic dermatitis
title_full Compensation of cATSCs-derived TGFβ1 and IL10 expressions was effectively modulated atopic dermatitis
title_fullStr Compensation of cATSCs-derived TGFβ1 and IL10 expressions was effectively modulated atopic dermatitis
title_full_unstemmed Compensation of cATSCs-derived TGFβ1 and IL10 expressions was effectively modulated atopic dermatitis
title_short Compensation of cATSCs-derived TGFβ1 and IL10 expressions was effectively modulated atopic dermatitis
title_sort compensation of catscs-derived tgfβ1 and il10 expressions was effectively modulated atopic dermatitis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3734835/
https://www.ncbi.nlm.nih.gov/pubmed/23412382
http://dx.doi.org/10.1038/cddis.2013.4
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