3 research outputs found
Distribution of nerve fibers and nerve-immune cell association in mouse spleen revealed by immunofluorescent staining
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
Immunofluorescent characterization of innervation and nerve-immune cell neighborhood in mouse thymus
The central nervous system impacts the immune system mainly by regulating the systemic concentration of humoral substances, whereas the peripheral nervous system (PNS) communicates with the immune system specifically according to local “hardwiring” of sympathetic/parasympathetic (efferent) and sensory (afferent) nerves to the primary and secondary lymphoid tissue/organs (e.g., thymus spleen and lymph nodes). In the present study, we use immunofluorescent staining of neurofilament-heavy to reveal the distribution of nerve fibers and the nerve-immune cell neighborhood inside the mouse thymus. Our results demonstrate (a) the presence of an extensive meshwork of nerve fibers in all thymic compartments, including the capsule, subcapsular region, cortex, cortico-medullary junction and medulla; (b) close associations of nerve fibers with blood vessels (including the postcapillary venules), indicating the neural control of blood circulation and immune cell dynamics inside the thymus; (c) the close proximity of nerve fibers to various subsets of thymocytes (e.g., CD4+, CD8+ and CD4+CD8+), dendritic cells (e.g., B220+, CD4+, CD8+ and F4/80+), macrophages (Mac1+ and F4/80+) and B cells. Our novel findings concerning thymic innervation and the nerve-immune cell neighborhood in situ should facilitate the understanding of bi-directional communications between the PNS and primary lymphoid organs. Since the innervation of lymphoid organs, including the thymus, may play essential roles in the pathogenesis and progression of some neuroimmune, infectious and autoimmune diseases, better knowledge of PNS-immune system crosstalk should benefit the development of potential therapies for these diseases
Innervation and nerve-immune cell contacts in mouse Peyer's patches
Neural regulation of the function of the
gastrointestinal tract (GIT) relies on a delicate balance of
the two divisions of its nervous system, namely, the
intrinsic and extrinsic divisions. The intrinsic
innervation is provided by the enteric nervous system
(ENS), whereas the extrinsic innervation includes
sympathetic/parasympathetic nerve fibers and extrinsic
sensory nerve fibers. In the present study, we used
immunofluorescent staining of neurofilament-heavy
(NF-H) to reveal the distribution of nerve fibers and
their associations with immune cells inside mouse
Peyer’s patches (PP), an essential part of gut-associated
lymphoid tissue (GALT). Our results demonstrate (1) the
presence of an extensive meshwork of NF-H-
immunoreactive presumptive nerve fibers in all PP
compartments including the lymphoid nodules,
interfollicular region, follicle-associated epithelium, and
subepithelial dome; (2) close associations/contacts of
nerve fibers with blood vessels including high
endothelial venules, indicating neural control of blood
flow and immune cell dynamics inside the PP; (3) close
contacts between nerve fibers/endings and B/T cells and
various subsets of dendritic cells (e.g., B220 - , B220 + ,
CD4 - , CD4 + , CD8 - , and CD8 + ). Our novel findings
concerning PP innervation and nerve-immune cell
contacts in situ should facilitate our understanding of bi-
directional communications between the PNS and
GALT. Since the innervation of the gut, including PP,
might be important in the pathogenesis and progression
of some neurological, infectious, and autoimmune
diseases, e.g., prion diseases and inflammatory bowel
disease, better knowledge of PNS-immune system
interactions in the GALT (including PP) should benefit
the development of potential treatments for these
diseases via neuroimmune manipulations