Maria Moura, Alice Miranda, Jonas Campos, Andreia G. Pinho, Sara Rito-Fernandes, Carina Soares-Cunha, António J. Salgado, Nuno A. Silva, Susana Monteiro
{"title":"Macro- and Microanatomy of the Sympathetic Innervation of the Spleen in Rodents","authors":"Maria Moura, Alice Miranda, Jonas Campos, Andreia G. Pinho, Sara Rito-Fernandes, Carina Soares-Cunha, António J. Salgado, Nuno A. Silva, Susana Monteiro","doi":"10.1002/cne.70086","DOIUrl":null,"url":null,"abstract":"<p>In recent years, several studies have demonstrated the crucial role played by the sympathetic spleen innervation in regulating immune cell function involving fighting pathogens or tissue injury. These findings have sparked interest across different research fields with a common goal of understanding and manipulating splenic sympathetic activity to modulate immune function and inflammation. However, the anatomical identification of spleen-projecting neurons in rodents presents a considerable challenge, given the multi-compartmentalized location of their cellular components.</p><p>This article addresses this challenge by providing a detailed anatomical dissection guide of the mouse celiac ganglion and splenic nerve, harboring the cell body and projecting axons, respectively. By combining antero- and retrograde neuronal tracing, immunofluorescence, 3D reconstruction, and viral tracing techniques, we validate the connectivity between the celiac ganglion and the spleen and provide insights into their microanatomy. Importantly, we demonstrate the feasibility of viral transduction in these neurons. Additionally, we identified nerve-associated macrophages (NAMs) within the splenic nerve and demonstrated their responsiveness to inflammatory stimuli. Our findings offer a comprehensive anatomical framework for studying spleen-projecting neurons, paving the way for future investigations into their role in immune regulation and inflammation, as well as their manipulation using advanced neurobiological tools.</p>","PeriodicalId":15552,"journal":{"name":"Journal of Comparative Neurology","volume":"533 9","pages":""},"PeriodicalIF":2.1000,"publicationDate":"2025-08-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cne.70086","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Comparative Neurology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cne.70086","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
In recent years, several studies have demonstrated the crucial role played by the sympathetic spleen innervation in regulating immune cell function involving fighting pathogens or tissue injury. These findings have sparked interest across different research fields with a common goal of understanding and manipulating splenic sympathetic activity to modulate immune function and inflammation. However, the anatomical identification of spleen-projecting neurons in rodents presents a considerable challenge, given the multi-compartmentalized location of their cellular components.
This article addresses this challenge by providing a detailed anatomical dissection guide of the mouse celiac ganglion and splenic nerve, harboring the cell body and projecting axons, respectively. By combining antero- and retrograde neuronal tracing, immunofluorescence, 3D reconstruction, and viral tracing techniques, we validate the connectivity between the celiac ganglion and the spleen and provide insights into their microanatomy. Importantly, we demonstrate the feasibility of viral transduction in these neurons. Additionally, we identified nerve-associated macrophages (NAMs) within the splenic nerve and demonstrated their responsiveness to inflammatory stimuli. Our findings offer a comprehensive anatomical framework for studying spleen-projecting neurons, paving the way for future investigations into their role in immune regulation and inflammation, as well as their manipulation using advanced neurobiological tools.
期刊介绍:
Established in 1891, JCN is the oldest continually published basic neuroscience journal. Historically, as the name suggests, the journal focused on a comparison among species to uncover the intricacies of how the brain functions. In modern times, this research is called systems neuroscience where animal models are used to mimic core cognitive processes with the ultimate goal of understanding neural circuits and connections that give rise to behavioral patterns and different neural states.
Research published in JCN covers all species from invertebrates to humans, and the reports inform the readers about the function and organization of nervous systems in species with an emphasis on the way that species adaptations inform about the function or organization of the nervous systems, rather than on their evolution per se.
JCN publishes primary research articles and critical commentaries and review-type articles offering expert insight in to cutting edge research in the field of systems neuroscience; a complete list of contribution types is given in the Author Guidelines. For primary research contributions, only full-length investigative reports are desired; the journal does not accept short communications.