ID | 112813 |
Title Alternative | TGF-β1 and IL-4 induce CCL11 production
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Author |
Hosokawa, Yoshitaka
Tokushima University
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Hosokawa, Ikuko
Tokushima University
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Ozaki, Kazumi
Tokushima University
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Keywords | CCL11
IL‐4
periodontal ligament cells
STAT6
TGF‐β1
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Content Type |
Journal Article
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Description | Transforming growth factor (TGF)-β1 is a multifunctional cytokine, which can control certain functions of various kinds of cells. However, it is unclear whether TGF-β1 affects T-cell migration in periodontal lesions. The aim of this study was to examine the effects of TGF-β1 on the production of C-C chemokine ligand (CCL)11, which is a T-helper 2-type chemokine, in human periodontal ligament cells (HPDLC). Interleukin (IL)-4 induced CCL11 production, but TGF-β1 did not, in HPDLC. However, TGF-β1 enhanced CCL11 production in IL-4-stimulated HPDLC. Western blot analysis showed that the signal transducer and activator of transcription 6 (STAT6) pathway was highly activated in HPDLC that had been stimulated with both IL-4 and TGF-β1. Mitogen-activated protein kinase activation did not differ between the HPDLC treated with a combination of IL-4 and TGF-β1 and those treated with IL-4 or TGF-β1 alone. Moreover, a STAT6 inhibitor significantly inhibited CCL11 production in HPDLC that had been stimulated with IL-4 and TGF-β1. The current study clearly demonstrated that TGF-β1 enhanced IL-4-induced CCL11 production in HPDLC. The STAT6 pathway is important for CCL11 production in IL-4- and TGF-β1-treated HPDLC.
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Journal Title |
Cell Biology International
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ISSN | 10656995
10958355
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NCID | AA10882014
AA11544414
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Publisher | International Federation for Cell Biology|Wiley
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Volume | 42
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Issue | 10
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Start Page | 1395
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End Page | 1400
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Published Date | 2018-07-24
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Remark | This is the peer reviewed version of the following article: Hosokawa, Y. , Hosokawa, I. , Ozaki, K. and Matsuo, T. (2018), Transforming growth factor‐β1 increases C‐C chemokine ligand 11 production in interleukin 4‐stimulated human periodontal ligament cells. Cell Biol Int, 42: 1395-1400, which has been published in final form at https://doi.org/10.1002/cbin.11030.
This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. |
Rights | © 2018 International Federation for Cell Biology
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DOI (Published Version) | |
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language |
eng
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Author
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departments |
Oral Sciences
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