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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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Autores principales: Peng, Meiyu, Zhang, Qi, Liu, Yanqing, Guo, Xiangdong, Ju, Jiyu, Xu, Lingzhi, Gao, Yuanyuan, Chen, Daquan, Mu, Dongzhen, Zhang, Rongxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7204910/
https://www.ncbi.nlm.nih.gov/pubmed/32425796
http://dx.doi.org/10.3389/fphar.2020.00576
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author Peng, Meiyu
Zhang, Qi
Liu, Yanqing
Guo, Xiangdong
Ju, Jiyu
Xu, Lingzhi
Gao, Yuanyuan
Chen, Daquan
Mu, Dongzhen
Zhang, Rongxin
author_facet Peng, Meiyu
Zhang, Qi
Liu, Yanqing
Guo, Xiangdong
Ju, Jiyu
Xu, Lingzhi
Gao, Yuanyuan
Chen, Daquan
Mu, Dongzhen
Zhang, Rongxin
author_sort Peng, Meiyu
collection PubMed
description 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 in vivo. After L-4F treatment, the differentiation, proliferation and apoptosis of MDSCs were detected in vitro. 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(2)O(2) 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.
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spelling pubmed-72049102020-05-18 Apolipoprotein A-I Mimetic Peptide L-4F Suppresses Granulocytic-Myeloid-Derived Suppressor Cells in Mouse Pancreatic Cancer Peng, Meiyu Zhang, Qi Liu, Yanqing Guo, Xiangdong Ju, Jiyu Xu, Lingzhi Gao, Yuanyuan Chen, Daquan Mu, Dongzhen Zhang, Rongxin Front Pharmacol Pharmacology 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 in vivo. After L-4F treatment, the differentiation, proliferation and apoptosis of MDSCs were detected in vitro. 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(2)O(2) 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. Frontiers Media S.A. 2020-04-30 /pmc/articles/PMC7204910/ /pubmed/32425796 http://dx.doi.org/10.3389/fphar.2020.00576 Text en Copyright © 2020 Peng, Zhang, Liu, Guo, Ju, Xu, Gao, Chen, Mu and Zhang http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Peng, Meiyu
Zhang, Qi
Liu, Yanqing
Guo, Xiangdong
Ju, Jiyu
Xu, Lingzhi
Gao, Yuanyuan
Chen, Daquan
Mu, Dongzhen
Zhang, Rongxin
Apolipoprotein A-I Mimetic Peptide L-4F Suppresses Granulocytic-Myeloid-Derived Suppressor Cells in Mouse Pancreatic Cancer
title Apolipoprotein A-I Mimetic Peptide L-4F Suppresses Granulocytic-Myeloid-Derived Suppressor Cells in Mouse Pancreatic Cancer
title_full Apolipoprotein A-I Mimetic Peptide L-4F Suppresses Granulocytic-Myeloid-Derived Suppressor Cells in Mouse Pancreatic Cancer
title_fullStr Apolipoprotein A-I Mimetic Peptide L-4F Suppresses Granulocytic-Myeloid-Derived Suppressor Cells in Mouse Pancreatic Cancer
title_full_unstemmed Apolipoprotein A-I Mimetic Peptide L-4F Suppresses Granulocytic-Myeloid-Derived Suppressor Cells in Mouse Pancreatic Cancer
title_short Apolipoprotein A-I Mimetic Peptide L-4F Suppresses Granulocytic-Myeloid-Derived Suppressor Cells in Mouse Pancreatic Cancer
title_sort apolipoprotein a-i mimetic peptide l-4f suppresses granulocytic-myeloid-derived suppressor cells in mouse pancreatic cancer
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7204910/
https://www.ncbi.nlm.nih.gov/pubmed/32425796
http://dx.doi.org/10.3389/fphar.2020.00576
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