4.6 Article

Cutting Edge: LL-37-Mediated Formyl Peptide Receptor-2 Signaling in Follicular Dendritic Cells Contributes to B Cell Activation in Peyer's Patch Germinal Centers

期刊

JOURNAL OF IMMUNOLOGY
卷 198, 期 2, 页码 629-633

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AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.1600886

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资金

  1. National Research Foundation - Korean Ministry of Science, ICT, and Future Planning [2014K1B1A1073861, 2014R1A1A3051207]
  2. Korea Health Industry Development Institute - Korean Ministry of Health and Welfare [HI15C3039]
  3. Research Base Construction Fund Support Program - Chonbuk National University
  4. Program of National University for Innovation and Transformation
  5. BK21 PLUS program in the Department of Bioactive Material Sciences
  6. National Research Foundation of Korea [2014K1B1A1073861, 2014R1A1A3051207] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

Peyer's patches (PPs) are the major mucosal immune-inductive site, and germinal centers (GCs) in PPs determine the quality of the Abs produced. PP GCs are continuously induced by the gut microbiota, and their maintenance contributes to the induction of strong IgA responses to Ags. In this study, we investigated the role of formyl peptide receptor (FPR)-mediated signaling in the maintenance of PP GCs, because FPRs recognize the microbiota and initiate an innate immune response by chemotaxis. We found that follicular dendritic cells (FDCs), a key organizer of B cell follicles and GCs in mucosal immunity, express Fpr2. Additionally, Fpr2-mediated signaling in PP FDCs promoted Cxcl13 and B cell activating factor expression, as well as B cell proliferation and activation. Therefore, we suggest that Fpr2-mediated signaling in FDCs plays a key role in GC maintenance in PPs and results in an Ag-specific IgA response in the gut mucosal immune compartment.

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