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Updated: Aug 19, 2026

Artificial Antigen Presenting Cell (aAPC) Mediated Activation and Expansion of Natural Killer T Cells
Published on: December 29, 2012
The mannose receptor is expressed by subsets of APC in non-lymphoid organs
1Sir William Dunn School of Pathology, South Parks Road, Oxford, OX1 3RE, UK. s.a.linehan@imperial.ac.uk
Background:
The mannose receptor (MR) is an endocytic receptor of Mphi and endothelial cell subsets whose natural ligands include both self glycoproteins and microbial glycans. It is also expressed by immature cultured dendritic cells (DC), where it mediates high efficiency uptake of glycosylated antigens, yet its role in antigen handling in vivo is unknown. Knowledge of which APC subsets express MR will assist the design of experiments to address its immunological functions. Here the expression of MR by MHC class II positive APC in non-lymphoid organs of the mouse is described.
Results:
MR positive APC were identified in several peripheral organs: skin, liver, cardiac and skeletal muscle and tongue. MR positive cells in salivary gland, thyroid and pancreas coexpressed MHC class II and the myeloid markers macrosialin and sialoadhesin, but not the dendritic cell markers CD11c or DEC-205. MR and MHC class II colocalised in confocal microscope images, implying that antigen capture may be the primary role of MR in these cells. Distinct ligands of MR were found in salivary gland and pancreas tissue lysates that are candidate physiological ligands of MR positive APC in these organs.
Conclusions:
The tissue and subcellular distribution of MR suggest it is appropriately located to serve as a high efficiency antigen uptake receptor of APC.
Insights
The mannose receptor (MR) is expressed by antigen-presenting cells (APCs) in mouse peripheral organs, suggesting a role in high-efficiency antigen uptake. This finding aids in understanding MR
Area of Science:
- Immunology
- Cell Biology
- Glycobiology
Background:
- The mannose receptor (MR) is an endocytic receptor found on macrophages and endothelial cells, binding self and microbial glycans.
- Its role in antigen uptake by antigen-presenting cells (APCs) in vivo remains unclear, despite expression on immature dendritic cells (DCs).
- Identifying MR-expressing APC subsets is crucial for investigating its immunological functions.
Purpose of the Study:
- To investigate the expression of the mannose receptor (MR) in major histocompatibility complex (MHC) class II-positive APCs within non-lymphoid organs of mice.
- To determine the cellular localization and potential function of MR in these peripheral APCs.
Main Methods:
- Immunohistochemistry and confocal microscopy were used to identify and localize MR-expressing cells.
- Co-expression analysis with myeloid and dendritic cell markers (macrosialin, sialoadhesin, CD11c, DEC-205) was performed.
- Analysis of tissue lysates for distinct MR ligands was conducted.
Main Results:
- MR-positive APCs were detected in various peripheral organs, including skin, liver, muscle, and tongue.
- In salivary glands, thyroid, and pancreas, MR-positive cells co-expressed MHC class II and myeloid markers but not DC markers.
- MR and MHC class II colocalization suggested a primary role in antigen capture, with identified tissue ligands supporting this function.
Conclusions:
- The tissue and subcellular distribution of MR indicate its suitability as a high-efficiency antigen uptake receptor for APCs.
- MR expression in peripheral APCs suggests a significant role in initiating immune responses against encountered antigens in non-lymphoid tissues.
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