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      NOX2-derived ROS-mediated surface translocation of BLT1 is essential for exocytosis in human eosinophils induced by LTB4.

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          Abstract

          Leukotriene B4 (LTB4) is a proinflammatory lipid mediator that elicits eosinophil exocytosis, leading to allergic inflammation. However, the detailed intracellular signaling mechanisms of eosinophil exocytosis induced by LTB4 are poorly understood. Herein, we report that NADPH oxidase (NOX)2-derived reactive oxygen species (ROS)-mediated BLT1 migration to the cell surface is required for exocytosis in human eosinophils induced by LTB4.

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          Author and article information

          Journal
          Int. Arch. Allergy Immunol.
          International archives of allergy and immunology
          S. Karger AG
          1423-0097
          1018-2438
          2014
          : 165
          : 1
          Affiliations
          [1 ] Department of Environmental Medical Biology, Yonsei University College of Medicine, Seoul, Republic of Korea.
          Article
          000366277
          10.1159/000366277
          25323785
          0d194e06-8e8d-4995-97b5-badf082a566f
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