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The influence of regulatory T cells on dendritic cells in mice with hepatocellular carcinoma |
DU Yong1, HUANG Zhiming2, LIN Xiuqing2, CHEN Xin2. |
1.Department of Pediatrics, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325015; 2.Department of Gastroenterology and Hepatology, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325015 |
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Cite this article: |
DU Yong,HUANG Zhiming,LIN Xiuqing, et al. The influence of regulatory T cells on dendritic cells in mice with hepatocellular carcinoma[J]. JOURNAL OF WEZHOU MEDICAL UNIVERSITY, 2017, 47(10): 718-722.
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Abstract Objective: To investigate how CD4+CD25+ regulatory T cells (Tregs)impacted on dendritic cells which were separated from BALB/c mice with hepatocellular carcinoma. Methods: BALB/c mice with hepatocellular carcinoma were established in laboratory. Twenty-five days after the models, the tumor-bearing mice were sacrificed and fresh spleen tissues were separated. Tregs, CD4+CD25-T cells and dendritic cells were separated from the mice’s spleen and purified by immuno-magnetic beads according to the manufacturers’ instructions. Tregs were co-cultured with CD4+CD25-T cells and the proliferation experiment was measured with CCK8. Tregs were directly co-cultured with dendritic cells and then the expression of CD80/CD86 on dendritic cells was detected by flow cytometry. The levels of TNF-α and IL-12 in supernatants were detected by ELISA. Results: We successfully established the tumor model of hepatocellular carcinoma and obtained high purity of Tregs, CD4+CD25-T cells and dendritic cells. Tregs could suppress the proliferation of CD4+CD25-T cells in vitro. Tregs could down-regulate the expression of CD80/CD86 on dendritic cells and inhibit the expression of TNF-α and IL-12. Conclusion: Tregs play an important role in the establishment and persistence of tumor immune suppression. Tregs can inhibit the function of dendritic cells in tumor-bearing mice. So Tregs may be a promising therapeutic target for cancer.
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Received: 14 March 2017
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