Prostate cancer cell-derived exosomes inhibit macrophage phagocytosis through EIF3B-mediated exosomal sorting of miR-100-5p

Abstract Exosomes play significant roles in the tumor microenvironment (TME). In particular, some exosomal microRNAs (miRNAs) have the ability to mediate macrophage polarization. However, the mechanism underlying the selective enrichment of miRNAs into exosomes remains largely unknown. Herein, we co...

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Main Authors: Yanyan Zhang, Yinying Hu, Hongyan Guo, Min Zhao, Shiqi Liu, Jing Liu, Yanqin Huang, Zhigang Wang
Format: Article
Language:English
Published: Nature Portfolio 2025-07-01
Series:Scientific Reports
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Online Access:https://doi.org/10.1038/s41598-025-11799-w
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author Yanyan Zhang
Yinying Hu
Hongyan Guo
Min Zhao
Shiqi Liu
Jing Liu
Yanqin Huang
Zhigang Wang
author_facet Yanyan Zhang
Yinying Hu
Hongyan Guo
Min Zhao
Shiqi Liu
Jing Liu
Yanqin Huang
Zhigang Wang
author_sort Yanyan Zhang
collection DOAJ
description Abstract Exosomes play significant roles in the tumor microenvironment (TME). In particular, some exosomal microRNAs (miRNAs) have the ability to mediate macrophage polarization. However, the mechanism underlying the selective enrichment of miRNAs into exosomes remains largely unknown. Herein, we compared the expression of miR-100-5p in exosomes derived from normal prostate epithelial cells and PC-3 cells. Subsequently, macrophages were treated with the aforementioned exosomes separately. Our results demonstrate that prostate cancer (PC)-derived exosomes can transfer miRNA-100-5p to macrophages and significantly increase miR-100-5p expression. To explore the role and mechanisms of exosomal miR-100-5p in macrophages, we performed phagocytosis assay and reactive oxygen species (ROS) detection experiment. Knockdown of miR-100-5p markedly promoted ROS generation in macrophages induced with PC-3 exosomes through the NADPH oxidase 4 (NOX4) pathway, leading to the increased phagocytosis of macrophages. Importantly, our results confirmed that eukaryotic translation initiation factor 3 subunit B (EIF3B) was highly expressed in PC cells and specifically bound to miR-100-5p by pull-down assay, and EIF3B knockdown decreased the enrichment of miR-100-5p in PC-3 exosomes. Collectively, our data showed that EIF3B-mediated selective sorting of miR-100-5p into PC exosomes reduced the generation of ROS by targeting NOX4 in macrophages, thus inhibiting macrophage phagocytosis. These findings reveal a new role for EIF3B in regulating the sorting of miR-100-5p into PC-3-derived exosomes, and identify an important new mode of TME regulation.
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spelling doaj-art-81b0366b4b6a466e90f553af168c02bb2025-08-20T03:05:17ZengNature PortfolioScientific Reports2045-23222025-07-0115111510.1038/s41598-025-11799-wProstate cancer cell-derived exosomes inhibit macrophage phagocytosis through EIF3B-mediated exosomal sorting of miR-100-5pYanyan Zhang0Yinying Hu1Hongyan Guo2Min Zhao3Shiqi Liu4Jing Liu5Yanqin Huang6Zhigang Wang7Medical College of Nanchang UniversityJiangxi Academy of Medical SciencesJiangxi Academy of Medical SciencesMedical College of Nanchang UniversityMedical College of Nanchang UniversityMedical College of Nanchang UniversityJiangxi Academy of Medical SciencesJiangxi Academy of Medical SciencesAbstract Exosomes play significant roles in the tumor microenvironment (TME). In particular, some exosomal microRNAs (miRNAs) have the ability to mediate macrophage polarization. However, the mechanism underlying the selective enrichment of miRNAs into exosomes remains largely unknown. Herein, we compared the expression of miR-100-5p in exosomes derived from normal prostate epithelial cells and PC-3 cells. Subsequently, macrophages were treated with the aforementioned exosomes separately. Our results demonstrate that prostate cancer (PC)-derived exosomes can transfer miRNA-100-5p to macrophages and significantly increase miR-100-5p expression. To explore the role and mechanisms of exosomal miR-100-5p in macrophages, we performed phagocytosis assay and reactive oxygen species (ROS) detection experiment. Knockdown of miR-100-5p markedly promoted ROS generation in macrophages induced with PC-3 exosomes through the NADPH oxidase 4 (NOX4) pathway, leading to the increased phagocytosis of macrophages. Importantly, our results confirmed that eukaryotic translation initiation factor 3 subunit B (EIF3B) was highly expressed in PC cells and specifically bound to miR-100-5p by pull-down assay, and EIF3B knockdown decreased the enrichment of miR-100-5p in PC-3 exosomes. Collectively, our data showed that EIF3B-mediated selective sorting of miR-100-5p into PC exosomes reduced the generation of ROS by targeting NOX4 in macrophages, thus inhibiting macrophage phagocytosis. These findings reveal a new role for EIF3B in regulating the sorting of miR-100-5p into PC-3-derived exosomes, and identify an important new mode of TME regulation.https://doi.org/10.1038/s41598-025-11799-wProstate cancerExosomemiRNA-100-5pEIF3BMacrophage
spellingShingle Yanyan Zhang
Yinying Hu
Hongyan Guo
Min Zhao
Shiqi Liu
Jing Liu
Yanqin Huang
Zhigang Wang
Prostate cancer cell-derived exosomes inhibit macrophage phagocytosis through EIF3B-mediated exosomal sorting of miR-100-5p
Scientific Reports
Prostate cancer
Exosome
miRNA-100-5p
EIF3B
Macrophage
title Prostate cancer cell-derived exosomes inhibit macrophage phagocytosis through EIF3B-mediated exosomal sorting of miR-100-5p
title_full Prostate cancer cell-derived exosomes inhibit macrophage phagocytosis through EIF3B-mediated exosomal sorting of miR-100-5p
title_fullStr Prostate cancer cell-derived exosomes inhibit macrophage phagocytosis through EIF3B-mediated exosomal sorting of miR-100-5p
title_full_unstemmed Prostate cancer cell-derived exosomes inhibit macrophage phagocytosis through EIF3B-mediated exosomal sorting of miR-100-5p
title_short Prostate cancer cell-derived exosomes inhibit macrophage phagocytosis through EIF3B-mediated exosomal sorting of miR-100-5p
title_sort prostate cancer cell derived exosomes inhibit macrophage phagocytosis through eif3b mediated exosomal sorting of mir 100 5p
topic Prostate cancer
Exosome
miRNA-100-5p
EIF3B
Macrophage
url https://doi.org/10.1038/s41598-025-11799-w
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