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The Regulating Effect of CII-3 and Its Active Components from Periplaneta americana on M1/M2 Macrophage Polarization

CII-3 is the effective part of Periplaneta americana for application in oncotherapy. This study investigated its main chemical components for macrophage polarization regulation activity. Compounds were separated and purified, and their structures were elucidated based on NMR and HR-ESI-MS analyses....

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Autores principales: Xu, Jinglei, Che, Yihao, Liu, Xinyue, Liu, Chaohe, Meng, Di, Pang, Xiuqin, He, Miao, Liu, Guangming, Zhang, Chenggui, Yang, Dasong, Xiao, Huai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9323847/
https://www.ncbi.nlm.nih.gov/pubmed/35889289
http://dx.doi.org/10.3390/molecules27144416
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author Xu, Jinglei
Che, Yihao
Liu, Xinyue
Liu, Chaohe
Meng, Di
Pang, Xiuqin
He, Miao
Liu, Guangming
Zhang, Chenggui
Yang, Dasong
Xiao, Huai
author_facet Xu, Jinglei
Che, Yihao
Liu, Xinyue
Liu, Chaohe
Meng, Di
Pang, Xiuqin
He, Miao
Liu, Guangming
Zhang, Chenggui
Yang, Dasong
Xiao, Huai
author_sort Xu, Jinglei
collection PubMed
description CII-3 is the effective part of Periplaneta americana for application in oncotherapy. This study investigated its main chemical components for macrophage polarization regulation activity. Compounds were separated and purified, and their structures were elucidated based on NMR and HR-ESI-MS analyses. After inducing the M1 and M2 phenotype macrophages, CII-3 and testing components were added and co-incubated to evaluate their effects on the relevant markers of macrophages. Then, gradient concentrations of CII-3 and active monomers were further investigated for their effects on M2 macrophages. The effects were detected by RT-PCR, ELISA, flow cytometry, and immunofluorescence. Twelve compounds were identified from CII-3. CII-3 and pericanaside (5) had no obvious effect on M1 macrophages, while they significantly reduced the expression levels of M2 macrophage markers. Specifically, they significantly reduced the levels of TGF-β and IL-10 and the mRNA expression levels of ARG-1 and CD206 in the M2 phenotypes of RAW264.7 and Ana-1 macrophages. The conditioned medium of CII-3 and pericanaside (5) could inhibit the migration capacity of CT26.WT tumor cells. Macrophage M1/M2 polarization is a dynamic equilibrium, and the M2 phenotype, which can promote the growth of tumor cells, is relatively highly expressed in the tumor microenvironment. CII-3 and pericanaside could significantly reduce the phenotype of M2-type macrophages, indicating that the anti-tumor activity of CII-3 could be related to the inhibitory effect on M2 polarization, and pericanaside was one of the active components.
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spelling pubmed-93238472022-07-27 The Regulating Effect of CII-3 and Its Active Components from Periplaneta americana on M1/M2 Macrophage Polarization Xu, Jinglei Che, Yihao Liu, Xinyue Liu, Chaohe Meng, Di Pang, Xiuqin He, Miao Liu, Guangming Zhang, Chenggui Yang, Dasong Xiao, Huai Molecules Article CII-3 is the effective part of Periplaneta americana for application in oncotherapy. This study investigated its main chemical components for macrophage polarization regulation activity. Compounds were separated and purified, and their structures were elucidated based on NMR and HR-ESI-MS analyses. After inducing the M1 and M2 phenotype macrophages, CII-3 and testing components were added and co-incubated to evaluate their effects on the relevant markers of macrophages. Then, gradient concentrations of CII-3 and active monomers were further investigated for their effects on M2 macrophages. The effects were detected by RT-PCR, ELISA, flow cytometry, and immunofluorescence. Twelve compounds were identified from CII-3. CII-3 and pericanaside (5) had no obvious effect on M1 macrophages, while they significantly reduced the expression levels of M2 macrophage markers. Specifically, they significantly reduced the levels of TGF-β and IL-10 and the mRNA expression levels of ARG-1 and CD206 in the M2 phenotypes of RAW264.7 and Ana-1 macrophages. The conditioned medium of CII-3 and pericanaside (5) could inhibit the migration capacity of CT26.WT tumor cells. Macrophage M1/M2 polarization is a dynamic equilibrium, and the M2 phenotype, which can promote the growth of tumor cells, is relatively highly expressed in the tumor microenvironment. CII-3 and pericanaside could significantly reduce the phenotype of M2-type macrophages, indicating that the anti-tumor activity of CII-3 could be related to the inhibitory effect on M2 polarization, and pericanaside was one of the active components. MDPI 2022-07-10 /pmc/articles/PMC9323847/ /pubmed/35889289 http://dx.doi.org/10.3390/molecules27144416 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Xu, Jinglei
Che, Yihao
Liu, Xinyue
Liu, Chaohe
Meng, Di
Pang, Xiuqin
He, Miao
Liu, Guangming
Zhang, Chenggui
Yang, Dasong
Xiao, Huai
The Regulating Effect of CII-3 and Its Active Components from Periplaneta americana on M1/M2 Macrophage Polarization
title The Regulating Effect of CII-3 and Its Active Components from Periplaneta americana on M1/M2 Macrophage Polarization
title_full The Regulating Effect of CII-3 and Its Active Components from Periplaneta americana on M1/M2 Macrophage Polarization
title_fullStr The Regulating Effect of CII-3 and Its Active Components from Periplaneta americana on M1/M2 Macrophage Polarization
title_full_unstemmed The Regulating Effect of CII-3 and Its Active Components from Periplaneta americana on M1/M2 Macrophage Polarization
title_short The Regulating Effect of CII-3 and Its Active Components from Periplaneta americana on M1/M2 Macrophage Polarization
title_sort regulating effect of cii-3 and its active components from periplaneta americana on m1/m2 macrophage polarization
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9323847/
https://www.ncbi.nlm.nih.gov/pubmed/35889289
http://dx.doi.org/10.3390/molecules27144416
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