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Silencing SOCS3 Markedly Deteriorates Spondyloarthritis in Mice Induced by Minicircle DNA Expressing IL23

Objective: Despite extensive studies, the precise mechanism underlying spondyloarthritis, especially ankylosing spondylitis, remains elusive. This study aimed to develop an ideal animal model for an insight into mechanism of spondyloarthritis and functional relevance of SOCS3 in spondyloarthritis. M...

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Autores principales: Chen, Yuhai, Ouyang, Jing, Yan, Ruoxiang, Maarouf, Mohamed Hassan, Wang, Xuefei, Chen, Biao, Liu, Shasha, Hu, Jiayue, Guo, Guijie, Zhang, Jing, Dai, Sheng-Ming, Xu, Huji, Chen, Ji-Long
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6246747/
https://www.ncbi.nlm.nih.gov/pubmed/30487798
http://dx.doi.org/10.3389/fimmu.2018.02641
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author Chen, Yuhai
Ouyang, Jing
Yan, Ruoxiang
Maarouf, Mohamed Hassan
Wang, Xuefei
Chen, Biao
Liu, Shasha
Hu, Jiayue
Guo, Guijie
Zhang, Jing
Dai, Sheng-Ming
Xu, Huji
Chen, Ji-Long
author_facet Chen, Yuhai
Ouyang, Jing
Yan, Ruoxiang
Maarouf, Mohamed Hassan
Wang, Xuefei
Chen, Biao
Liu, Shasha
Hu, Jiayue
Guo, Guijie
Zhang, Jing
Dai, Sheng-Ming
Xu, Huji
Chen, Ji-Long
author_sort Chen, Yuhai
collection PubMed
description Objective: Despite extensive studies, the precise mechanism underlying spondyloarthritis, especially ankylosing spondylitis, remains elusive. This study aimed to develop an ideal animal model for an insight into mechanism of spondyloarthritis and functional relevance of SOCS3 in spondyloarthritis. Methods: Since SOCS3 is a major regulator of IL23-STAT3 signaling, we generated SOCS3 knockdown transgenic (TG) mice for development of an animal model of spondyloarthritis. A hydrodynamic delivery method was employed to deliver minicircle DNA expressing IL23 (mc-IL23) into wild-type (WT) and the TG mice. Knockdown/overexpression systems mediated by lentivirus and retrovirus were used to determine whether SOCS3 regulated osteoblast differentiation. Results: Forced expression of IL23 induced severe joint destruction and extensive bone loss in SOCS3 knockdown TG mice, while this treatment only caused moderate symptoms in WT mice. Furthermore, severe spondyloarthritis was found in IL23-injected TG mice as compared to mild disease observed in WT controls under same condition. Moreover, our studies showed that IL23 promoted osteoblast differentiation via activation of STAT3 pathway and disruption of SOCS3 expression greatly increased phosphorylation of STAT3. In addition, silencing SOCS3 resulted in enhanced osteoblast differentiation through activation of Smad1/5/9 signaling, as evidenced by elevated phosphorylation level of Smad1/5/9. Experiments further demonstrated that SOCS3 interacted with Smad1 and thus suppressed the BMP2-Smad signaling. Conclusions: The results reveal that SOCS3 is involved in IL23-induced spondyloarthritis and acts as a key regulator of osteoblast differentiation, and suggest that SOCS3 knockdown TG mice may be an ideal animal model for further studies of spondyloarthritis.
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spelling pubmed-62467472018-11-28 Silencing SOCS3 Markedly Deteriorates Spondyloarthritis in Mice Induced by Minicircle DNA Expressing IL23 Chen, Yuhai Ouyang, Jing Yan, Ruoxiang Maarouf, Mohamed Hassan Wang, Xuefei Chen, Biao Liu, Shasha Hu, Jiayue Guo, Guijie Zhang, Jing Dai, Sheng-Ming Xu, Huji Chen, Ji-Long Front Immunol Immunology Objective: Despite extensive studies, the precise mechanism underlying spondyloarthritis, especially ankylosing spondylitis, remains elusive. This study aimed to develop an ideal animal model for an insight into mechanism of spondyloarthritis and functional relevance of SOCS3 in spondyloarthritis. Methods: Since SOCS3 is a major regulator of IL23-STAT3 signaling, we generated SOCS3 knockdown transgenic (TG) mice for development of an animal model of spondyloarthritis. A hydrodynamic delivery method was employed to deliver minicircle DNA expressing IL23 (mc-IL23) into wild-type (WT) and the TG mice. Knockdown/overexpression systems mediated by lentivirus and retrovirus were used to determine whether SOCS3 regulated osteoblast differentiation. Results: Forced expression of IL23 induced severe joint destruction and extensive bone loss in SOCS3 knockdown TG mice, while this treatment only caused moderate symptoms in WT mice. Furthermore, severe spondyloarthritis was found in IL23-injected TG mice as compared to mild disease observed in WT controls under same condition. Moreover, our studies showed that IL23 promoted osteoblast differentiation via activation of STAT3 pathway and disruption of SOCS3 expression greatly increased phosphorylation of STAT3. In addition, silencing SOCS3 resulted in enhanced osteoblast differentiation through activation of Smad1/5/9 signaling, as evidenced by elevated phosphorylation level of Smad1/5/9. Experiments further demonstrated that SOCS3 interacted with Smad1 and thus suppressed the BMP2-Smad signaling. Conclusions: The results reveal that SOCS3 is involved in IL23-induced spondyloarthritis and acts as a key regulator of osteoblast differentiation, and suggest that SOCS3 knockdown TG mice may be an ideal animal model for further studies of spondyloarthritis. Frontiers Media S.A. 2018-11-14 /pmc/articles/PMC6246747/ /pubmed/30487798 http://dx.doi.org/10.3389/fimmu.2018.02641 Text en Copyright © 2018 Chen, Ouyang, Yan, Maarouf, Wang, Chen, Liu, Hu, Guo, Zhang, Dai, Xu and Chen. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Chen, Yuhai
Ouyang, Jing
Yan, Ruoxiang
Maarouf, Mohamed Hassan
Wang, Xuefei
Chen, Biao
Liu, Shasha
Hu, Jiayue
Guo, Guijie
Zhang, Jing
Dai, Sheng-Ming
Xu, Huji
Chen, Ji-Long
Silencing SOCS3 Markedly Deteriorates Spondyloarthritis in Mice Induced by Minicircle DNA Expressing IL23
title Silencing SOCS3 Markedly Deteriorates Spondyloarthritis in Mice Induced by Minicircle DNA Expressing IL23
title_full Silencing SOCS3 Markedly Deteriorates Spondyloarthritis in Mice Induced by Minicircle DNA Expressing IL23
title_fullStr Silencing SOCS3 Markedly Deteriorates Spondyloarthritis in Mice Induced by Minicircle DNA Expressing IL23
title_full_unstemmed Silencing SOCS3 Markedly Deteriorates Spondyloarthritis in Mice Induced by Minicircle DNA Expressing IL23
title_short Silencing SOCS3 Markedly Deteriorates Spondyloarthritis in Mice Induced by Minicircle DNA Expressing IL23
title_sort silencing socs3 markedly deteriorates spondyloarthritis in mice induced by minicircle dna expressing il23
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6246747/
https://www.ncbi.nlm.nih.gov/pubmed/30487798
http://dx.doi.org/10.3389/fimmu.2018.02641
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