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The Mechanism of Interleukin 33-Induced Stimulation of Interleukin 6 in MLO-Y4 Cells

The differentiation and function of osteocytes are controlled by surrounding cells and mechanical stress; however, the detailed mechanisms are unknown. Recent findings suggest that IL-33 is highly expressed in periodontal tissues in orthodontic tooth movement. The present study aimed to elucidate th...

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Autores principales: Noguchi, Sae, Yamasaki, Ryota, Nagai-Yoshioka, Yoshie, Sato, Tsuyoshi, Kuroishi, Kayoko, Gunjigake, Kaori, Ariyoshi, Wataru, Kawamoto, Tatsuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10573633/
https://www.ncbi.nlm.nih.gov/pubmed/37834290
http://dx.doi.org/10.3390/ijms241914842
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author Noguchi, Sae
Yamasaki, Ryota
Nagai-Yoshioka, Yoshie
Sato, Tsuyoshi
Kuroishi, Kayoko
Gunjigake, Kaori
Ariyoshi, Wataru
Kawamoto, Tatsuo
author_facet Noguchi, Sae
Yamasaki, Ryota
Nagai-Yoshioka, Yoshie
Sato, Tsuyoshi
Kuroishi, Kayoko
Gunjigake, Kaori
Ariyoshi, Wataru
Kawamoto, Tatsuo
author_sort Noguchi, Sae
collection PubMed
description The differentiation and function of osteocytes are controlled by surrounding cells and mechanical stress; however, the detailed mechanisms are unknown. Recent findings suggest that IL-33 is highly expressed in periodontal tissues in orthodontic tooth movement. The present study aimed to elucidate the effect of IL-33 on the expression of regulatory factors for bone remodeling and their molecular mechanisms in the osteocyte-like cell line MLO-Y4. MLO-Y4 cells were treated with IL-33, and the activation of intracellular signaling molecules and transcriptional factors was determined using Western blot analysis and chromatin immunoprecipitation assay. IL-33 treatment enhanced the expression of IL-6 in MLO-Y4 cells, which was suppressed by the knockdown of the IL-33 receptor ST2L. Additionally, IL-33 treatment induced activation of NF-κB, JNK/AP-1, and p38 MAPK signaling pathways in MLO-Y4 cells. Moreover, pretreatment with specific inhibitors of NF-κB, p38 MAPK, and JNK/AP-1 attenuated the IL-33-induced expression of IL-6. Furthermore, chromatin immunoprecipitation indicated that IL-33 increased c-Jun recruitment to the IL-6 promoter. Overall, these results suggest that IL-33 induces IL-6 expression and regulates osteocyte function via activation of the NF-κB, JNK/AP-1, and p38 MAPK pathways through interaction with ST2L receptors on the plasma membrane.
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spelling pubmed-105736332023-10-14 The Mechanism of Interleukin 33-Induced Stimulation of Interleukin 6 in MLO-Y4 Cells Noguchi, Sae Yamasaki, Ryota Nagai-Yoshioka, Yoshie Sato, Tsuyoshi Kuroishi, Kayoko Gunjigake, Kaori Ariyoshi, Wataru Kawamoto, Tatsuo Int J Mol Sci Article The differentiation and function of osteocytes are controlled by surrounding cells and mechanical stress; however, the detailed mechanisms are unknown. Recent findings suggest that IL-33 is highly expressed in periodontal tissues in orthodontic tooth movement. The present study aimed to elucidate the effect of IL-33 on the expression of regulatory factors for bone remodeling and their molecular mechanisms in the osteocyte-like cell line MLO-Y4. MLO-Y4 cells were treated with IL-33, and the activation of intracellular signaling molecules and transcriptional factors was determined using Western blot analysis and chromatin immunoprecipitation assay. IL-33 treatment enhanced the expression of IL-6 in MLO-Y4 cells, which was suppressed by the knockdown of the IL-33 receptor ST2L. Additionally, IL-33 treatment induced activation of NF-κB, JNK/AP-1, and p38 MAPK signaling pathways in MLO-Y4 cells. Moreover, pretreatment with specific inhibitors of NF-κB, p38 MAPK, and JNK/AP-1 attenuated the IL-33-induced expression of IL-6. Furthermore, chromatin immunoprecipitation indicated that IL-33 increased c-Jun recruitment to the IL-6 promoter. Overall, these results suggest that IL-33 induces IL-6 expression and regulates osteocyte function via activation of the NF-κB, JNK/AP-1, and p38 MAPK pathways through interaction with ST2L receptors on the plasma membrane. MDPI 2023-10-02 /pmc/articles/PMC10573633/ /pubmed/37834290 http://dx.doi.org/10.3390/ijms241914842 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Noguchi, Sae
Yamasaki, Ryota
Nagai-Yoshioka, Yoshie
Sato, Tsuyoshi
Kuroishi, Kayoko
Gunjigake, Kaori
Ariyoshi, Wataru
Kawamoto, Tatsuo
The Mechanism of Interleukin 33-Induced Stimulation of Interleukin 6 in MLO-Y4 Cells
title The Mechanism of Interleukin 33-Induced Stimulation of Interleukin 6 in MLO-Y4 Cells
title_full The Mechanism of Interleukin 33-Induced Stimulation of Interleukin 6 in MLO-Y4 Cells
title_fullStr The Mechanism of Interleukin 33-Induced Stimulation of Interleukin 6 in MLO-Y4 Cells
title_full_unstemmed The Mechanism of Interleukin 33-Induced Stimulation of Interleukin 6 in MLO-Y4 Cells
title_short The Mechanism of Interleukin 33-Induced Stimulation of Interleukin 6 in MLO-Y4 Cells
title_sort mechanism of interleukin 33-induced stimulation of interleukin 6 in mlo-y4 cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10573633/
https://www.ncbi.nlm.nih.gov/pubmed/37834290
http://dx.doi.org/10.3390/ijms241914842
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