Nagisa Yoshida, Anna Appios, Qian Li, Joseph P. Hutton, George Wood, Martin Potts, Julia Aleksandrowicz, Enrico R. Barrozo, Freya Dover, Holly Anderson, Katie Stephens, Irving L. M. H. Aye, Jake R. Thomas, Hannah C. M. Schenk, Adam M. Bourke, Catherine E. Aiken, Ashley Moffett, Andrew Sharkey, Anna V. Protasio, Kjersti M. Aagaard, James R. Edgar, Betty Y. W. Chung, Naomi McGovern
{"title":"Interactions between placental Hofbauer cells and L. monocytogenes change throughout gestation","authors":"Nagisa Yoshida, Anna Appios, Qian Li, Joseph P. Hutton, George Wood, Martin Potts, Julia Aleksandrowicz, Enrico R. Barrozo, Freya Dover, Holly Anderson, Katie Stephens, Irving L. M. H. Aye, Jake R. Thomas, Hannah C. M. Schenk, Adam M. Bourke, Catherine E. Aiken, Ashley Moffett, Andrew Sharkey, Anna V. Protasio, Kjersti M. Aagaard, James R. Edgar, Betty Y. W. Chung, Naomi McGovern","doi":"10.1126/sciimmunol.adq3066","DOIUrl":null,"url":null,"abstract":"<div >Hofbauer cells (HBCs) are extraembryonic macrophages generated de novo within the human placenta. In this study, we explored how the properties of HBCs change throughout gestation. Our analysis revealed transcriptomic differences between first-trimester and term HBCs, with many of the altered genes linked to immune responses. As pregnancy progresses, HBCs exhibit a marked decrease in phagosome maturation and acidification. We show that the differences between first-trimester and term HBCs are important in the context of infection with <i>Listeria monocytogenes</i>, a pathogen that crosses the placenta and replicates within macrophages. Specifically, we observed reduced colony-forming units and diminished actin recruitment by <i>L. monocytogenes</i> in first-trimester HBCs compared with term HBCs. Our findings indicate that the ability of <i>L. monocytogenes</i> to escape from vacuoles is impaired within first-trimester HBCs. Thus, the changes in HBC biology across pregnancy are important in shaping their interactions with <i>L. monocytogenes.</i></div>","PeriodicalId":21734,"journal":{"name":"Science Immunology","volume":"10 109","pages":""},"PeriodicalIF":17.6000,"publicationDate":"2025-07-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.science.org/doi/reader/10.1126/sciimmunol.adq3066","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science Immunology","FirstCategoryId":"3","ListUrlMain":"https://www.science.org/doi/10.1126/sciimmunol.adq3066","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Hofbauer cells (HBCs) are extraembryonic macrophages generated de novo within the human placenta. In this study, we explored how the properties of HBCs change throughout gestation. Our analysis revealed transcriptomic differences between first-trimester and term HBCs, with many of the altered genes linked to immune responses. As pregnancy progresses, HBCs exhibit a marked decrease in phagosome maturation and acidification. We show that the differences between first-trimester and term HBCs are important in the context of infection with Listeria monocytogenes, a pathogen that crosses the placenta and replicates within macrophages. Specifically, we observed reduced colony-forming units and diminished actin recruitment by L. monocytogenes in first-trimester HBCs compared with term HBCs. Our findings indicate that the ability of L. monocytogenes to escape from vacuoles is impaired within first-trimester HBCs. Thus, the changes in HBC biology across pregnancy are important in shaping their interactions with L. monocytogenes.
期刊介绍:
Science Immunology is a peer-reviewed journal that publishes original research articles in the field of immunology. The journal encourages the submission of research findings from all areas of immunology, including studies on innate and adaptive immunity, immune cell development and differentiation, immunogenomics, systems immunology, structural immunology, antigen presentation, immunometabolism, and mucosal immunology. Additionally, the journal covers research on immune contributions to health and disease, such as host defense, inflammation, cancer immunology, autoimmunity, allergy, transplantation, and immunodeficiency. Science Immunology maintains the same high-quality standard as other journals in the Science family and aims to facilitate understanding of the immune system by showcasing innovative advances in immunology research from all organisms and model systems, including humans.