Abstract

The central nervous system regulates the immune system through the secretion of hormones from the pituitary gland and other endocrine organs, while the peripheral nervous system (PNS) communicates with the immune system through local nerve-immune cell interactions, including sympathetic/parasympathetic (efferent) and sensory (afferent) innervation to lymphoid tissue/organs. However, the precise mechanisms of this bi-directional crosstalk of the PNS and immune system remain mysterious. To study this kind of bi-directional crosstalk, we performed immunofluorescent staining of neurofilament and confocal microscopy to reveal the distribution of nerve fibers and nerve-immune cell associations inside mouse spleen. Our study demonstrates (i) extensive nerve fibers in all splenic compartments including the splenic nodules, periarteriolar lymphoid sheath, marginal zones, trabeculae, and red pulp; (ii) close associations of nerve fibers with blood vessels (including central arteries, marginal sinuses, penicillar arterioles, and splenic sinuses); (iii) close associations of nerve fibers with various subsets of dendritic cells, macrophages (Mac1+ and F4/80+), and lymphocytes (B cells, T helper cells, and cytotoxic T cells). Our data concerning the extensive splenic innervation and nerve-immune cell communication will enrich our knowledge of the mechanisms through which the PNS affects the cellular- and humoral-mediated immune responses in healthy and infectious/non-infectious states.

Highlights

  • The central nervous system regulates the immune system through the secretion of hormones from the pituitary gland and other endocrine organs, while the peripheral nervous system (PNS) communicates with the immune system through local nerve-immune cell interactions, including sympathetic/parasympathetic and sensory innervation to lymphoid tissue/organs

  • By using immunofluorescent staining and confocal microscopy/three-dimensional (3D) reconstruction, we have investigated the distribution of nerve fibers and PNS-immune cell relationship in situ in the mouse spleen to improve our knowledge of the microanatomical basis of bi-directional communication of the PNS and secondary lymphoid tissue/organs

  • We found an extensive meshwork of nerve fibers in splenic compartments including the capsule, splenic nodules (B cell follicles), marginal zones, periarteriolar lymphoid sheath (PALS), and red pulps (Figs. 1 and 2)

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Summary

Introduction

The central nervous system regulates the immune system through the secretion of hormones from the pituitary gland and other endocrine organs, while the peripheral nervous system (PNS) communicates with the immune system through local nerve-immune cell interactions, including sympathetic/parasympathetic (efferent) and sensory (afferent) innervation to lymphoid tissue/organs. The precise mechanisms of this bi-directional crosstalk of the PNS and immune system remain mysterious To study this kind of bi-directional crosstalk, we performed immunofluorescent staining of neurofilament and confocal microscopy to reveal the distribution of nerve fibers and nerveimmune cell associations inside mouse spleen. The PNS can regulate the development, deployment, and homeostatic regulation of the immune system[3] This type of local neuroimmune interaction involves the “hardwiring” of sympathetic/parasympathetic (efferent) and visceral sensory (afferent) nerves to primary and secondary lymphoid tissue/organs[4,5,6]. In the adult nervous system, NFs in small unmyelinated axons contain more peripherin and less NF-H, whereas NFs in large myelinated axons contain more NF-H and less peripherin

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