Interleukin-17 Indirectly Promotes M2 Macrophage Differentiation through Stimulation of COX-2/PGE2 Pathway in the Cancer Cells.
- Author:
Qingli LI
1
;
Lunxu LIU
;
Qiuyang ZHANG
;
Sen LIU
;
Dongxia GE
;
Zongbing YOU
Author Information
1. Departments of Structural and Cellular Biology and Orthopaedic Surgery, Tulane Cancer Center and Louisiana Cancer Research Consortium, Tulane Center for Stem Cell Research and Regenerative Medicine, and Tulane Center for Aging, Tulane University Health Sc
- Publication Type:Original Article
- Keywords:
Interleukin-17;
Cyclooxygenase-2;
Dinoprostone;
Neoplasms;
Macrophages;
Tumor microenvironment
- MeSH:
Animals;
Autoimmunity;
Blotting, Western;
Cell Line;
Cyclooxygenase 2;
Dinoprostone;
Enzyme-Linked Immunosorbent Assay;
Humans;
Inflammation;
Interleukin-10;
Interleukin-17*;
Lung Neoplasms;
Macrophages*;
Mice;
Monocytes;
Nitric Oxide Synthase Type II;
Prostatic Neoplasms;
Real-Time Polymerase Chain Reaction;
RNA, Messenger;
Tumor Microenvironment;
Tumor Necrosis Factor-alpha;
Up-Regulation;
Uterine Cervical Neoplasms
- From:Cancer Research and Treatment
2014;46(3):297-306
- CountryRepublic of Korea
- Language:English
-
Abstract:
PURPOSE: Interleukin-17 (IL-17) is a proinflammatory cytokine that plays important roles in inflammation, autoimmunity, and cancer. The purpose of this study was to determine if IL-17 indirectly regulates macrophage differentiation through up-regulation of cyclooxygenase-2 (COX-2) expression in the cancer cell lines. MATERIALS AND METHODS: Human cervical cancer HeLa, human lung cancer A549, and mouse prostate cancer Myc-CaP/CR cell lines were treated with recombinant IL-17; Western blot analysis, enzyme-linked immunosorbent assay, and quantitative real-time polymerase chain reaction analysis were utilized to examine the cellular responses. RESULTS: IL-17 up-regulated expression of COX-2 mRNA and protein in HeLa, A549, and Myc-CaP/CR cell lines. IL-17's effects were mediated through nuclear factor-kappaB and ERK1/2 signaling pathways as the inhibitors of these pathways could inhibit IL-17-induced COX-2 expression. The conditional medium obtained from the cancer cells contained prostaglandin E2, the levels of which were increased by IL-17 treatment. When treated with the conditional medium, particularly with the IL-17-induced conditional medium, mouse RAW264.7 macrophages and human THP-1 monocytes expressed higher levels of IL-10 (a marker of M2 macrophages) than inducible nitric oxide synthase or tumor necrosis factor alpha (markers of M1 macrophages). In contrast, when RAW264.7 and THP-1 cells were treated directly with IL-17, expression of these marker genes was not markedly changed. CONCLUSION: The results of this study suggest that IL-17 indirectly promotes M2 macrophage differentiation through stimulation of the COX-2/PGE2 pathway in the cancer cells, thus IL-17 plays an indirect role in regulating the tumor immune microenvironment.
