Apolipoprotein A-I Mimetic Peptide L-4F Suppresses Granulocytic-Myeloid-Derived Suppressor Cells in Mouse Pancreatic Cancer

L-4F is an apolipoprotein A-I (ApoA-I) mimetic peptide, it was engineered to imitate the anti-inflammatory and anti-oxidative activity of ApoA-I. In this paper, H7 cell was used to construct a mouse model of pancreatic cancer in situ, and the mice were treated with L-4F. Then, the development of pan...

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Veröffentlicht in:Frontiers in pharmacology 2020-04, Vol.11, p.576-576
Hauptverfasser: Peng, Meiyu, Zhang, Qi, Liu, Yanqing, Guo, Xiangdong, Ju, Jiyu, Xu, Lingzhi, Gao, Yuanyuan, Chen, Daquan, Mu, Dongzhen, Zhang, Rongxin
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Sprache:eng
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Zusammenfassung:L-4F is an apolipoprotein A-I (ApoA-I) mimetic peptide, it was engineered to imitate the anti-inflammatory and anti-oxidative activity of ApoA-I. In this paper, H7 cell was used to construct a mouse model of pancreatic cancer in situ, and the mice were treated with L-4F. Then, the development of pancreatic cancer and myeloid-derived suppressor cells (MDSCs) infiltration were investigated . After L-4F treatment, the differentiation, proliferation and apoptosis of MDSCs were detected . Moreover, we test its effects on the immunosuppressive function of MDSCs ex vivo. The results show that L-4F significantly reduced the tumorigenicity of H7 cells. L-4F suppressed granulocytic myeloid-derived suppressor cells (PMN-MDSCs) differentiation and inhibited the accumulation of PMN-MDSCs in the mouse spleen and tumor tissue. L-4F weakened the immunosuppressive function of MDSCs, resulting in decreased production of ROS and H O by MDSCs, and increased T cell proliferation, interferon γ and tumor necrosis factor β secretion, and CD3 CD4 T and CD3 CD8 T cell infiltration into the mouse spleen and pancreatic cancer tissue. Furthermore, L-4F significantly down regulated the STAT3 signaling pathway in PMN-MDSCs. These results indicated that L-4F exerts an effective anti-tumor and immunomodulatory effect in pancreatic cancer by inhibiting PMN-MDSCs.
ISSN:1663-9812
1663-9812
DOI:10.3389/fphar.2020.00576