Macro‐ and Microanatomy of the Sympathetic Innervation of the Spleen in Rodents

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.

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Publication Details

Journal
The Journal of Comparative Neurology
Published
2025-08-29
DOI
https://doi.org/10.1002/cne.70086
Primary Topic
Vagus Nerve Stimulation Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Macro‐ and Microanatomy of the Sympathetic Innervation of the Spleen in Rodents

Susana Monteiro, Alice Miranda, Andreia G. Pinho, Maria Ivete de Moura et al.
The Journal of Comparative Neurology
Vagus Nerve Stimulation Research
article

Macro‐ and Microanatomy of the Sympathetic Innervation of the Spleen in Rodents

Susana Monteiro, Alice Miranda, Andreia G. Pinho, Maria Ivete de Moura, Carina Soares‐Cunha, Sara R. M. Fernandes, António José Salgado, Jonas Campos, Nuno André Silva
article en

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.

The Journal of Comparative NeurologyVol. 533(9)
University of Minho (PT)
Wings for Life, “la Caixa” Foundation, Wings for Life, Santa Casa da Misericórdia de Lisboa, Fundação para a Ciência e a Tecnologia
Openalex Percentile: Top 72%
Vagus Nerve Stimulation Research
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