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ORIGINAL RESEARCH article

Front. Nutr.

Sec. Nutritional Immunology

Volume 12 - 2025 | doi: 10.3389/fnut.2025.1545720

This article is part of the Research Topic Immunonutrition: Bridging Precision Nutrition and Modern Medicine View all 9 articles

Retinoic Acid Modulates Peritoneal Macrophage Function and Distribution to Enhance Antib acterial Defense During Inflammation

Provisionally accepted
Yujuan Qin Yujuan Qin 1Xi Wang Xi Wang 2Xiamin Zhang Xiamin Zhang 1Lianting Nong Lianting Nong 3Qiyan Hou Qiyan Hou 3Chen Yuhong Chen Yuhong 3Yuting Li Yuting Li 3Wenxian Lin Wenxian Lin 3Xiuli Mao Xiuli Mao 3Kezhao Wu Kezhao Wu 3Wenqian Nong Wenqian Nong 3Tonghua Wang Tonghua Wang 1*Lingzhang Meng Lingzhang Meng 3*Jian Song Jian Song 4*
  • 1 Graduate School, Youjiang Medical College for Nationalities, Baise, China
  • 2 Guangxi University, Nanning, Guangxi Zhuang Region, China
  • 3 The People’s Hospital of Guangxi Zhuang Autonomous Region & Guangxi Academy of Medical Sciences, Nanning, China
  • 4 University Hospital Münster, Münster, Germany

The final, formatted version of the article will be published soon.

    Background:Peritoneal macrophages, comprising large peritoneal macrophages (LPMs) and small peritoneal macrophages (SPMs), play a vital role in maintaining immune defenses during inflammation. However, the molecular mechanisms governing their responses, particularly the impact of retinoic acid (RA), remain poorly understood. This study aims to elucidate the role of RA in modulating macrophage function, distribution, and immune responses during bacterial infections.Methods:A murine model of peritonitis was established using Escherichia coli expressing a tdTomato fluorescence marker. The effects of RA on macrophage phagocytic capacity, population dynamics, and transcriptomic profiles were assessed using immunofluorescence, flow cytometry, RNA sequencing, and quantitative PCR. Additionally, RA-loaded ZIF-8 nanoparticles were employed to investigate the sustained effects of RA delivery.Results:RA significantly enhanced macrophage phagocytic activity, delayed functional decline, and promoted the recruitment of SPMs in the peritoneal cavity. Transcriptomic analysis revealed upregulation of leukocyte migration and cell adhesion pathways in RA-treated SPMs. RA treatment also induced distinct gene expression profiles in macrophage subpopulations, reflecting its role in immune modulation. Notably, RA-loaded ZIF-8 nanoparticles prolonged RA retention within macrophages, sustaining its effects.Conclusions:RA enhances antibacterial defense by modulating macrophage activity, providing new insights into immune regulation. These findings underscore the therapeutic potential of RA and its nanoparticle formulations in managing bacterial infections and inflammation. 

    Keywords: Peritonitis, large peritoneal macrophages, small peritoneal macrophages, Retinoic acid, Nanoparticles

    Received: 15 Dec 2024; Accepted: 07 Apr 2025.

    Copyright: © 2025 Qin, Wang, Zhang, Nong, Hou, Yuhong, Li, Lin, Mao, Wu, Nong, Wang, Meng and Song. 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) or licensor 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.

    * Correspondence:
    Tonghua Wang, Graduate School, Youjiang Medical College for Nationalities, Baise, 533000, China
    Lingzhang Meng, The People’s Hospital of Guangxi Zhuang Autonomous Region & Guangxi Academy of Medical Sciences, Nanning, China
    Jian Song, University Hospital Münster, Münster, Germany

    Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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