Abstract

BackgroundThe neonatal Fc receptor (FcRn) plays a crucial role in transporting IgG and associated antigens across polarized epithelial barriers in mucosal immunity. However, it was not clear that FcRn expression in aggregated lymphoid nodules area (ALNA) in abomasum, a unique and important mucosal immune structure discovered only in Bactrian camels. In the present study, 27 Alashan Bactrian camels were divided into the following five age groups: fetus (10–13 months of gestation), young (1–2 years), pubertal (3–5 years), middle-aged (6–16 years) and old (17–20 years). The FcRn expressions were observed and analyzed in detail with histology, immunohistochemistry, micro-image analysis and statistical methods.ResultsThe results showed that the FcRn was expressed in mucosal epithelial cells of ALNA from the fetus to the old group, although the expression level rapidly declined in old group; moreover, after the ALNA maturated, the FcRn expression level in the non-follicle-associated epithelium (non-FAE) was significantly higher than that in FAE (P < 0.05). In addition, the FcRn was also expressed in the vessel endothelium, smooth muscle tissue, and macrophages and dendritic cells (DCs) of secondary lymphoid follicles (sLFs).ConclusionsIt was demonstrated that FcRn was mainly expressed in non-FAE, the effector sites, although which was expressed in FAE, the inductive sites for mucosal immunity. And it was also expressed in DCs and macrophages in sLFs of all ages of Bactrian camels. The results provided a powerful evidence that IgG (including HCAb) could participate in mucosal immune response and tolerance in ALNA of Bactrian camels through FcRn transmembrane transport.

Highlights

  • The neonatal Fc receptor (FcRn) plays a crucial role in transporting IgG and associated antigens across polarized epithelial barriers in mucosal immunity

  • (1') In reticular mucosal folds region (RMFR), a plenty of primary lymphatic follicles were primary densely-distributed in the lamina propria (LP) (Fig. 1)

  • Typical macrophages and dendritic cells (DCs) with high Neonatal Fc receptor (FcRn) expression were not observed in the primary lymphatic follicles (pLFs) (Fig. 2c)

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Summary

Introduction

The neonatal Fc receptor (FcRn) plays a crucial role in transporting IgG and associated antigens across polarized epithelial barriers in mucosal immunity. The neonatal Fc receptor (FcRn) plays a crucial role in transporting IgG and associated antigens across polarized barriers [6,7,8,9,10,11] In human intestinal epithelial cells, FcRn is expressed in both fetus and adult [15, 26] By contrast, it is only highly in newborns and the level rapidly declines after weaning in mouse [27, 28]. The range of animals in which FcRn orthologs have been identified includes rabbit [29], pig [30], sheep [31], bovine [32], Egyptian water buffalo [33], and dromedary [34]

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