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一种吲哚酚化合物5-溴-4-氯-3-吲哚基1,3-二乙酸酯(CAC-0982)可抑制肥大细胞中Fyn激酶的激活以及小鼠体内IgE介导的过敏反应。

An indoxyl compound 5-bromo-4-chloro-3-indolyl 1,3-diacetate, CAC-0982, suppresses activation of Fyn kinase in mast cells and IgE-mediated allergic responses in mice.

作者信息

Lee Jun Ho, Kim Tae Hyung, Kim Hyuk Soon, Kim A-Ram, Kim Do-Kyun, Nam Seung Taek, Kim Hyun Woo, Park Young Hwan, Her Erk, Park Yeong Min, Kim Hyung Sik, Kim Young Mi, Choi Wahn Soo

机构信息

Department of Immunology, School of Medicine, Konkuk University, Chungju 380-701, Republic of Korea; College of Medicine, Korea University, Seoul 136-701, Republic of Korea.

College of Pharmacy, Sungkyunkwan University, Suwon 440-746, Republic of Korea.

出版信息

Toxicol Appl Pharmacol. 2015 Jun 15;285(3):179-86. doi: 10.1016/j.taap.2015.04.009. Epub 2015 Apr 19.

Abstract

Mast cells, constituents of virtually all organs and tissues, are critical cells in IgE-mediated allergic responses. The aim of this study was to investigate the effect and mechanism of an indoxyl chromogenic compound, 5-bromo-4-chloro-3-indolyl 1,3-diacetate, CAC-0982, on IgE-mediated mast cell activation and allergic responses in mice. CAC-0982 reversibly suppressed antigen-stimulated degranulation in murine mast cells (IC50, ~3.8μM) and human mast cells (IC50, ~3.0μM). CAC-0982 also inhibited the expression and secretion of IL-4 and TNF-α in mast cells. Furthermore, CAC-0982 suppressed the mast cell-mediated allergic responses in mice in a dose-dependent manner (ED50 27.9mg/kg). As for the mechanism, CAC-0982 largely suppressed the phosphorylation of Syk and its downstream signaling molecules, including LAT, Akt, Erk1/2, p38, and JNK. Notably, the tyrosine kinase assay of antigen-stimulated mast cells showed that CAC-0982 inhibited Fyn kinase, one of the upstream tyrosine kinases for Syk activation in mast cells. Taken together, these results suggest that CAC-0982 may be used as a new treatment for regulating IgE-mediated allergic diseases through the inhibition of the Fyn/Syk pathway in mast cells.

摘要

肥大细胞是几乎所有器官和组织的组成部分,是IgE介导的过敏反应中的关键细胞。本研究的目的是探讨吲哚显色化合物5-溴-4-氯-3-吲哚基1,3-二乙酸酯(CAC-0982)对小鼠IgE介导的肥大细胞活化和过敏反应的作用及机制。CAC-0982可逆性抑制小鼠肥大细胞(IC50,约3.8μM)和人肥大细胞(IC50,约3.0μM)中抗原刺激的脱颗粒。CAC-0982还抑制肥大细胞中IL-4和TNF-α的表达和分泌。此外,CAC-0982以剂量依赖性方式抑制小鼠肥大细胞介导的过敏反应(ED50 27.9mg/kg)。至于机制,CAC-0982在很大程度上抑制了Syk及其下游信号分子(包括LAT、Akt、Erk1/2、p38和JNK)的磷酸化。值得注意的是,抗原刺激的肥大细胞的酪氨酸激酶测定表明,CAC-0982抑制Fyn激酶,Fyn激酶是肥大细胞中Syk激活的上游酪氨酸激酶之一。综上所述,这些结果表明,CAC-0982可能通过抑制肥大细胞中的Fyn/Syk途径用作调节IgE介导的过敏性疾病的新疗法。

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