Cordycepin Suppresses Thymic Stromal Lymphopoietin Expression via Blocking Caspase-1 and Receptor-Interacting Protein 2 Signaling Pathways in Mast Cells
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- Yoou Myoung-schook
- Department of Pharmacology, College of Korean Medicine, Kyung Hee University
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- Jin Mu Hyun
- Skin Research Center, Research Park, LG Household & Healthcare Ltd.
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- Lee So Young
- Skin Research Center, Research Park, LG Household & Healthcare Ltd.
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- Lee Sang Hwa
- Skin Research Center, Research Park, LG Household & Healthcare Ltd.
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- Kim Byunghyun
- Skin Research Center, Research Park, LG Household & Healthcare Ltd.
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- Roh Seok Seon
- Whoo Oriental Herb & Skin Research Society College of Korean Medicine, Daejeon University
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- Choi In Hwa
- Whoo Oriental Herb & Skin Research Society Department of Oriental Dermatology, College of Korean Medicine, Kyung Hee University
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- Lee Myeong Soo
- Whoo Oriental Herb & Skin Research Society Korea Institute of Oriental Medicine
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- Kim Hyung-Min
- Department of Pharmacology, College of Korean Medicine, Kyung Hee University Whoo Oriental Herb & Skin Research Society
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- Jeong Hyun-Ja
- Department of Food Technology and Biochip Research Center, Hoseo University
書誌事項
- タイトル別名
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- Cordycepin Suppresses Thymic Stromal Lymphopoietin Expression <i>via</i> Blocking Caspase-1 and Receptor-Interacting Protein 2 Signaling Pathways in Mast Cells
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抄録
Cordycepin (3′-deoxyadenosine) is one of the active components isolated from Cordyceps militaris, and has been shown to have anti-inflammatory, anti-oxidant, anti-aging, and anti-cancer effects. Mast cell-derived thymic stromal lymphopoietin (TSLP) plays an important role in the pathogenesis of allergic inflammatory reactions. Here, we investigated the regulatory effect and mechanisms of cordycepin on the expression of TSLP in the human mast cell line, HMC-1 cells, and in the human keratinocyte cell line, HaCaT cells. Cordycepin significantly decreased the production and mRNA expression of TSLP through the inhibition of caspase-1 and nuclear factor-κB activation. Cordycepin also significantly reduced the phosphorylation of receptor-interacting protein 2 and inhibitory kappa B (IκB) kinase β. Cordycepin significantly decreased the production and mRNA expression of interleukin (IL)-8, IL-1β, IL-6, and tumor necrosis factor-α in activated HMC-1 cells. Moreover, cordycepin significantly decreased the levels of TSLP in activated HaCaT cells. Our studies suggest that cordycepin can be applied to the treatment of allergic inflammatory diseases exacerbated by TSLP.
収録刊行物
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- Biological & Pharmaceutical Bulletin
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Biological & Pharmaceutical Bulletin 39 (1), 90-96, 2016
公益社団法人 日本薬学会
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詳細情報 詳細情報について
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- CRID
- 1390282679609053696
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- NII論文ID
- 130005116499
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- NII書誌ID
- AA10885497
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- ISSN
- 13475215
- 09186158
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- NDL書誌ID
- 027013092
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- PubMed
- 26725432
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- NDL
- Crossref
- PubMed
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可