4.6 Article

Calcitonin Gene-Related Peptide and Cyclic Adenosine 5′-Monophosphate/Protein Kinase A Pathway Promote IL-9 Production in Th9 Differentiation Process

期刊

JOURNAL OF IMMUNOLOGY
卷 190, 期 8, 页码 4046-4055

出版社

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.1203102

关键词

-

资金

  1. Ministry of Education, Culture, Sports, Science, and Technology of Japan [22590062]
  2. Japan Chemical Industry Association Long-Range Research Initiative
  3. Osaka Foundation for Promotion of Clinical Immunology
  4. Japan Society for the Promotion of Science fellows
  5. Grants-in-Aid for Scientific Research [22590062] Funding Source: KAKEN

向作者/读者索取更多资源

Th9 cells are a novel Th cell subset that produces IL-9 and is involved in type I hypersensitivity such as airway inflammation. Although its critical roles in asthma have attracted interest, the physiological regulatory mechanisms of Th9 cell differentiation and function are largely unknown. Asthma is easily affected by psychological factors. Therefore, we investigated one of the physiological mediators derived from the nervous system, calcitonin gene-related peptide (CGRP), in asthma and Th9 cells because CGRP and activation of the cAMP/protein kinase A (PKA) pathway by CGRP are known to be important regulators in several immune responses and allergic diseases. In this study, we demonstrated that the CGRP/cAMP/PKA pathway promotes IL-9 production via NFATc2 activation by PKA-dependent glycogen synthase kinase-3 beta inactivation. Moreover, CGRP also induces the expression of PU.1, a critical transcriptional factor in Th9 cells, which depends on PKA, but not NFATc2. Additionally, we demonstrated the physiological importance of CGRP in IL-9 production and Th9 differentiation using an OVA-induced airway inflammation model and T cell-specific CGRP receptor-deficient mice. The present study revealed a novel regulatory mechanism comprising G protein-coupled receptor ligands and nervous system-derived substances in Th9 cell differentiation and type I hypersensitivity. The Journal of Immunology, 2013, 190: 4046-4055.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据