Cordycepin Suppresses Thymic Stromal Lymphopoietin Expression via Blocking Caspase-1 and Receptor-Interacting Protein 2 Signaling Pathways in Mast Cells

  • Yoou Myoung-schook
    Department of Pharmacology, College of Korean Medicine, Kyung Hee University
  • Jin Mu Hyun
    Skin Research Center, Research Park, LG Household & Healthcare Ltd.
  • Lee So Young
    Skin Research Center, Research Park, LG Household & Healthcare Ltd.
  • Lee Sang Hwa
    Skin Research Center, Research Park, LG Household & Healthcare Ltd.
  • Kim Byunghyun
    Skin Research Center, Research Park, LG Household & Healthcare Ltd.
  • Roh Seok Seon
    Whoo Oriental Herb & Skin Research Society College of Korean Medicine, Daejeon University
  • Choi In Hwa
    Whoo Oriental Herb & Skin Research Society Department of Oriental Dermatology, College of Korean Medicine, Kyung Hee University
  • Lee Myeong Soo
    Whoo Oriental Herb & Skin Research Society Korea Institute of Oriental Medicine
  • Kim Hyung-Min
    Department of Pharmacology, College of Korean Medicine, Kyung Hee University Whoo Oriental Herb & Skin Research Society
  • Jeong Hyun-Ja
    Department of Food Technology and Biochip Research Center, Hoseo University

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タイトル別名
  • 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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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.

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