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WZ3146 inhibits mast cell Lyn and Fyn to reduce IgE-mediated allergic responses in vitro and in vivo.
Park, Young Hwan; Kim, Do Kyun; Kim, Hyuk Soon; Lee, Dajeong; Lee, Min Bum; Min, Keun Young; Jo, Min Geun; Lee, Ji Eon; Kim, Young Mi; Choi, Wahn Soo.
Afiliação
  • Park YH; Department of Immunology, College of Medicine, Konkuk University, Chungju 27478, Republic of Korea.
  • Kim DK; Department of Immunology, College of Medicine, Konkuk University, Chungju 27478, Republic of Korea.
  • Kim HS; Department of Immunology, College of Medicine, Konkuk University, Chungju 27478, Republic of Korea.
  • Lee D; Department of Immunology, College of Medicine, Konkuk University, Chungju 27478, Republic of Korea.
  • Lee MB; Department of Immunology, College of Medicine, Konkuk University, Chungju 27478, Republic of Korea.
  • Min KY; Department of Immunology, College of Medicine, Konkuk University, Chungju 27478, Republic of Korea.
  • Jo MG; Department of Immunology, College of Medicine, Konkuk University, Chungju 27478, Republic of Korea.
  • Lee JE; Department of Immunology, College of Medicine, Konkuk University, Chungju 27478, Republic of Korea.
  • Kim YM; College of Pharmacy, Duksung Women's University, Seoul 01369, Republic of Korea.
  • Choi WS; Department of Immunology, College of Medicine, Konkuk University, Chungju 27478, Republic of Korea. Electronic address: wahnchoi@kku.ac.kr.
Toxicol Appl Pharmacol ; 383: 114763, 2019 11 15.
Article em En | MEDLINE | ID: mdl-31526816
ABSTRACT
Mast cells (MCs) play an important role as effector cells that cause allergic responses in allergic diseases. For these reasons, MC is considered an attractive therapeutic target for allergic disease treatment. In this study, we investigated the inhibitory effect of WZ3146, N-[3-[5-chloro-2-[4-(4-methylpiperazin-1-yl)anilino]pyrimidin-4-yl]oxyphenyl]prop-2-enamide, and the mechanisms of its actions on the MC activation and IgE-mediated allergic response by using three types of MCs such as rat basophilic leukemia (RBL)-2H3 cells, mouse bone marrow mast cells (BMMCs), and human Laboratory of Allergic Diseases 2 (LAD2) cells. WZ3146 inhibited antigen-stimulated degranulation in a dose-dependent manner (IC50, ~ 0.35 µM for RBL-2H3 cells; ~ 0.39 µM for BMMCs; ~ 0.41 for LAD2 cells). WZ3146 also suppressed the production of histamine, tumor necrosis factor (TNF)-α and interleukin (IL)-6, which mediate various allergic responses, in a dose-dependent manner. As the mechanism of WZ3146 to inhibit MCs, it inhibited the activation of spleen tyrosine kinase (Syk) and the downstream signaling proteins of Syk such as linker for activation of T cell (LAT) and phospholipase (PL) Cγ1 in the signaling pathway of FcεRI. In addition, WZ3146 inhibited the activation of Akt, extracellular signal-regulated kinase (ERK)1/2, p38, and c-Jun N-terminal kinase (JNK). However, WZ3146 did not inhibit degranulation of MCs by thapsigargin or ionomycin, which increase calcium concentration in cytosol. Notably, WZ3146 inhibited the activity of Lyn and Fyn, but not Syk. In an following animal experiment, WZ3146 inhibited IgE-dependent passive cutaneous anaphylaxis (PCA) in a dose-dependent manner (ED50, ~ 20 mg/kg). Taken together, in this study we show that the pyrimidine derivative, WZ3146, inhibits the IgE-mediated allergic response by inhibiting Lyn and Fyn Src-family kinases, which are initially activated by antigen stimulation in MCs. Therefore, we propose that WZ3146 could be used as a new therapeutic agent for the treatment of allergic diseases.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pirimidinas / Imunoglobulina E / Quinases da Família src / Proteínas Proto-Oncogênicas c-fyn / Hipersensibilidade / Mastócitos Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pirimidinas / Imunoglobulina E / Quinases da Família src / Proteínas Proto-Oncogênicas c-fyn / Hipersensibilidade / Mastócitos Idioma: En Ano de publicação: 2019 Tipo de documento: Article