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Central European Journal of Immunology
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vol. 39

Experimental immunology
An anti-DEC-205 monoclonal antibody stimulates binding of thymocytes to rat thymic dendritic cells and promotes apoptosis of thymocytes

Ivana Majstorović
Dragana Vučević
Bojan Pavlović
Saša Vasilijić
Miodrag Čolić

(Centr Eur J Immunol 2014; 39 (4): 411-418)
Online publish date: 2014/12/15
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T-cell differentiation and repertoire selection in the thymus are essential for the establishment and maintenance of the adaptive immune system, and play a critical role in immunological tolerance [1].
The mechanisms of positive and negative selection are central for the generation of self-tolerant T-cells, capable of recognizing foreign antigens in the context of self-MHC molecules [2]. These processes require various inputs from surrounding thymic stromal cells composed of thymic epithelial cells (TEC), thymic dendritic cells (TDC), macrophages and other cells (fibroblasts, endothelial cells, etc.) which provide an array of optimal signals to developing thymocytes. Substantial evidence now supports the notion that major inducers of positive selection of thymocytes are cortical TEC, whereas TDC and medullary TEC contribute to the negative selection [3]. Many of the signals required for different stages of intrathymic development are provided by thymic stromal cells in the form of cell surface molecules [1]. Although intrathymic T-cell differentiation and selection have been an area of intense investigation, the molecular and cellular mechanisms of these processes are not resolved yet.
Previous investigations have shown that DEC-205 (CD205), a 205 kDa integral membrane glycoprotein, positively discriminates cortical TEC [4, 5]. Expression of DEC-205 was detected also on antigen presenting cells, especially on DC in many different tissues including TDC [4, 6]. Studies investigating the CD205 expression by peripheral DC have demonstrated that CD205 operates as an antigen uptake and processing receptor [5]. Human and mouse DEC-205 antigen exhibits approximately 80% protein homology, suggesting its conserved function between species [7]. Park et al. [8] successfully generated anti-human DEC-205 monoclonal antibodies (mAbs), produced from human DEC-205-immunized DEC-205 knock-out mice, which were species cross-reactive. One of these mAbs, named HD83, was found to recognize DEC-205 antigen in rat spleen and lymph node [8]. To date, there has been no report on the expression status and the potential functional significance of DEC-205 in the rat thymus.
In an attempt to delineate the function of rat DEC-205 in thymocyte development we characterized its expression within the rat thymus by using HD83 mAb and an immunohistochemical approach. We also analyzed the adhesive interactions between thymocytes and TDC in vitro and showed that HD83 mAb enhanced the binding of thymocytes to TDC and stimulated thymocyte apoptosis.
These results suggest the possible molecular mechanisms through which DEC-205 antigen may influence T-cell development and selection in the thymus.

Material and methods


Autoshaping-operant (AO) rats, male, 6-8 weeks old, bred at the Farm for Experimental Animals, Military Medical Academy (MMA) (Belgrade, Serbia) were used in this study. The study was approved by the Ethical Committee of MMA, Belgrade, Serbia, according to the Guidelines for Animal Study, No 282-12/2002.


The following mouse anti-rat monoclonal antibodies (mAbs) were used: HD83, mouse anti-DEC-205 mAb cross-reactive with human, mouse, monkey and rat DEC-205 antigen, a kind gift from Dr. Chae Gyu Park (Severance Biomedical Science Institute, Yonsei University College of Medicine, Korea) [8] and OX-6 mAb, (anti I-A) (Serotec). As an irrelevant mAb, the isotype matching mAb VAM 4.1, reactive with Pseudorabies virus and nonreactive with rat antigens, produced at the Institute for Medical Research, MMA, Belgrade, was used. Horseradish peroxidase (HRP)-conjugated rabbit anti-mouse immunoglobulin (Ig) was purchased from Dako, Denmark.


Cryostat sections (6-8 µm) of rat thymus were fixed in acetone for 10 minutes at –20°C, air dried and rehydrated in 50 mM Tris-buffered saline (TBS) pH 7.6. Slides were then incubated overnight at 4°C with appropriate dilutions of mAbs (final concentrations 10 µg/ml for all tested mAbs) and washed in TBS. After that, incubation with HRP-conjugated rabbit anti-mouse Ig (1 : 25) in TBS containing 5% normal rat serum for 30 minutes followed. After washing in TBS the specific immunolabeling was visualized by adding 0.06% diaminobenzidine (DAB) (Serva) and 0.01% hydrogen peroxide (Sigma) in TBS. Finally, the sections were washed and then lightly counterstained with haematoxylin, prior to mounting. Micrographs of stained thymus sections were taken under the conventional light microscope (Olympus, BX 41). The specificity of immunostaining was confirmed by omission of primary mAb.


Cytospins of TDC rosettes were fixed in pararosaniline for 2 minutes, washed in TBS and incubated with appropriate dilution of HD83 mAb (10 µg/ml) for 60 minutes. After washing in TBS, slides were incubated with HRP-conjugated rabbit anti-mouse Ig (1 : 25) with addition of 5% normal rat serum. Specific immunolabeling was visualized by adding 0.06% diaminobenzidine (DAB) (Serva) and 0.01% hydrogen peroxide (Sigma) as already described. The slides were lightly counterstained with haematoxylin, prior to mounting. The control was VAM 4.1, used as an irrelevant mAb at the same concentration.

Thymic dendritic cells preparation and cultivation

Thymic dendritic cells were isolated from rat thymuses by using the method previously described by Vasilijic et al.[9]. Briefly, 4 ml of thymocyte cell suspension (3-4 × 108 cells) was overlaid on 3 ml of OptiPrep™ gradient (Nycomed Pharma AS, Oslo, Norway) (density 1.078 g/ml and osmolarity 390 mOsm). Cells were then centrifuged at 600 γ for 15 min at 4°C and TDC fraction was collected at the RPMI medium/Optiprep interface. The purity of such prepared TDC was 40%, as checked by morphology. Contaminating cells were mostly thymocytes and macrophages. To further enrich the TDC suspension, TDC were cultivated overnight in 6-well plates (Flow, ICN) at a concentration of 1.5 × 106 cells/ml of RPMI 1640 medium supplemented with 10% fetal calf serum (FCS) and 5 ng/ml mouse recombinant granulocyte macrophage-colony stimulating factor (rGM-CSF) (Genzime, Boston, USA) at 37°C and 5% CO2. Thymic dendritic cells were collected as non-adherent cells, resuspended in warm RPMI 1640 medium with 0.02% Na-EDTA and purified again over OptiPrepTM density gradient (Sigma). After washing twice in RPMI 1640 with 2% FCS, the TDC suspension was counted and analyzed in Turk’s solution under the microscope. The purity of cultivated TDC was around 80%.


To prepare thymocytes, the thymus was teased with a syringe plunge, cells were collected, filtered through a nylon mesh, centrifuged for 10 minutes at 600 × g, and washed in 1640 RPMI medium with 2% FCS. The thymocyte suspension was counted, and cell viability, which was higher than 95%, was checked by Trypan blue exclusion.

Rosette assay

Thymic dendritic cells (5 × 104) were preincubated with HD83 mAb, control VAM 4.1 mAb (both at the concentrations of 10 µg/ml), or medium alone for 15 min, then mixed with freshly isolated thymocytes (2.5 × 105), 1 : 5 ratio, in 20 µl of the complete medium, transferred into a Terasaki microwell plate and cultured in a hanging drop. After 30 minutes of incubation at 37°C and 5% CO2, the cells were gently collected and cytocentrifuged onto glass slides. Cytospins were stained with May-Grunwald Giemsa (MGG) and analyzed by light microscopy. Thymic dendritic cells that bound three or more thymocytes were scored as rosettes. For each assay 200-500 TDC were counted and each determination was performed in duplicate. Two parameters were determined: rosette formation (represented by the percentage of TDC forming rosettes in comparison with a total number of TDC) and mean number of thymocytes per rosette.

Apoptosis assays

Purified cultivated TDC were mixed with syngeneic thymocytes at 1 : 5 ratio and cultivated in RPMI 1640 medium with 10% FCS in 96-well flat bottom plates. HD83 mAb or control VAM 4.1 mAb (both 10 µg/ml) were added to TDC/thymocyte co-cultures. After 6 h incubation thymocyte apoptosis was measured. The percentage of apoptotic thymocytes, identified in TDC/thymocyte co-cultures, was determined by morphological criteria as previously described [10] and AnnexinV-FITC/Propidium Iodide (PI) method. For morphological evaluation, thymocytes cultivated with TDC were washed with PBS, fixed with Turck’s solution and analyzed by light microscopy. In each sample at least 500 cells were counted. Apoptotic cells were identified by condensation of chromatin, nuclear pyknosis and/or karyorrhexis. The results were expressed as a percentage of apoptotic thymocytes relative to total counted thymocytes. For cytometric determination of thymocyte apoptosis, cells were stained with AnnexinV-FITC/PI kit KXN50 (R&D, Abingdon, Oxon, UK). Cells from each well were stained according to the manufacturer’s instructions and analyzed using a flow cytometer (CyFlow Cube 6, Partec, Germany). Double negative cells are viable cells, AnnexinV-FITC+/PI– cells represent thymocytes in the early stage of apoptosis, double positive cells are late apoptotic/secondary necrotic thymocytes, whereas only PI+ cells are primarily necrotic cells.
Apoptosis of thymocytes within TDC rosettes on cytospins prepared after 30 minutes of incubation, was determined also based on morphological criteria. The results were expressed as % of apoptotic thymocytes within rosettes relative to total thymocytes bound to TDC.

Statistical analysis

Results were expressed as mean ± SD. Statistical analysis was performed by t-test. P < 0.05 was considered statistically significant.


Expression of DEC-205 antigen in the rat thymus

The sections of rat thymuses were stained with HD83 mAb. Results presented in Figure 1 clearly show that this antibody stains cortical epithelium and isolated stellate or ramified cells in the medulla, resembling TDC. The staining of the cortex was stronger than in the medulla, especially on the border of epithelial-free zones, which were clearly negative, and at the cortico-medullary zones. Subcapsular epithelial cells, perivascular epithelial cells in the cortex and medullary epithelial cells were DEC-205 negative. By comparing the staining of the thymus with OX-6 mAb (an anti-rat MHC class II molecule antibody), it can be seen that both cortical and medullary epithelial cells, including subcapsular/perivascular TEC, TDC in the medulla and macrophage-like cells throughout the whole section, including macrophages within epithelial-free zones, express MHC class II molecules.
The positive immunoreaction of isolated thymic nurse cells (TNC) and TDC (Fig. 2), and negative staining of both viable and apoptotic thymocytes by HD83 mAb (data not shown), confirmed the pattern expression of the DEC-205 antigen seen in situ.

HD83 mAb stimulates the formation of rosettes between thymocytes and thymic dendritic cells

To study possible functional roles of the DEC-205 antigen in the thymus, we performed a rosette assay between thymocytes and TDC in vitro. Figure 3 shows that HD83 mAb stimulates the rosette formation, compared to corresponding controls, as judged by either the percentage of TDC forming rosettes or by the mean number of thymocytes per rosette. HD83 mAb stimulates apoptosis of thymocytes Thymocytes die rapidly in culture and the apoptotic process was accelerated in co-culture with TDC. Both morphological and flow-cytometric methods gave similar results (Fig. 4A and 4B). When HD83 mAb was added to the co-culture, apoptosis of thymocytes was further increased, compared to controls. The process was more evident when early stage apoptotic cells (AnnexinV-FITC+/PI–) were analyzed (Fig. 4B). To check whether this process was associated with increased adhesiveness of thymocytes to TDC, apoptosis was measured separately in rosettes. It can be seen that the percentage of apoptotic thymocytes in rosettes was higher compared to apoptosis of total thymocytes. The percentage of apoptotic thymocytes in rosettes (stimulated in the presence of HD83 mAb) was statistically significantly higher compared to the percentage of apoptotic thymocytes in rosettes in control cultures (without HD83 mAb or in the presence of Ir mAb). This finding suggests that the increased formation of TDC/thymocyte rosettes was associated with increased apoptosis of thymocytes within these cell-to-cell clusters.


The first mAb produced against mouse DEC-205, NLDC-145, has been shown to stain cortical TEC and medullary TDC [11]. Subsequent studies confirmed the expression of DEC-205 on mouse DC in other lymphoid organs, especially on the CD8+ DC subset and weakly on other antigen-presenting cells (macrophages and B-cells) [4, 12-14]. Later on, the study in the human system showed distribution of DEC-205 on other cells, including myeloid blood DC and monocytes, but also at low levels on natural killer cells, plasmacytoid DC and T-cells [6]. Since the data related to DEC-205 expression in the rat system are very scarce [8], the first aim of this study was to characterize the expression of this molecule in the rat thymus. By using an immunohistochemical approach on rat thymus sections and isolated cells, we confirmed that the pattern expression of DEC-205 closely resembled that in the mouse thymus. Namely, cortical TEC, including TNC, and medullary TDC were strongly DEC-205 positive. It is interesting that subcapsular and perivascular epithelial cells in the cortex were DEC-205 negative. In contrast, all thymic epithelial structures, TDC and macrophages were MHC class II positive. These findings, together with negative staining of medullary TEC with HD83 mAb are in accordance with already published phenotypic heterogeneity of TEC [15]. An extensive immunohistochemical study demonstrated that subcapsular/perivascular and most medullary TEC share the same phenotype, in contrast to the cortical TEC, which express some specific markers [15]. It is obvious that such a unique cortical TEC-subset-specific marker is DEC-205.
It is known that DEC-205 belongs to the macrophage mannose receptor family of C-type lectin endocytic receptors, which behaves as an antigen-uptake/processing receptor for DC and cortical TEC [5]. Its predominant function is to direct capture of antigens from the extracellular space to a specialized antigen-processing compartment [16]. Based on these results it can be postulated that DEC-205 must have a role in endocytosis and subsequent processing of self-antigens in the thymus. Such mechanisms are important for selection processes in the thymus [17]. A paper published by Small and Kraal [18] showed an in vitro evidence for participation of DEC-205 in clearance of apoptotic thymocytes by mouse cortical TEC. Later on, such a role has been postulated for mouse CD8+ DC subset, which selectively enodocytoses dying cells in culture and in vivo [14]. This finding is very important because CD8+ DC, in contrast to CD8– DC, are specialized to capture dying cells and to cross-present cellular antigens to both CD4+ and CD8+ T-cells, where DEC-205 might have a very important role. The ligands for DEC-205 in the tissue have not been identified yet. The only paper that deals with this research area showed evidence that CpG oligonucleotides, well known pathogen associated molecular pattern and a selective TLR-9 agonist, bind to both mouse and human DEC-205 [19]. It has been recently confirmed that apoptotic thymocytes express ligands for mouse DEC-205, as demonstrated by using a DEC-205 – Ig fusion protein [20].
All these results motivated us to study the possible role of rat DEC-205 in the processes of thymocyte apoptosis. Our previous results showed that rat TDC in culture stimulated apoptosis of thymocytes. This process was associated with binding of thymocytes to TDC and was partially blocked by a LFA-1 mAb [21]. Such results were confirmed later by other authors [22] by demonstrating the involvement of TDC- and thymic macrophages-derived NO, as an important effector mechanism in apoptosis induction of rat thymocytes. To see whether DEC-205 interferes with binding of thymocytes to TDC, we performed a rosette assay and demonstrated that HD83 mAb significantly increased these cell-to-cell adhesive interactions. The process was associated with increased apoptosis of thymocytes in co-culture with TDC and with an increased percentage of apoptotic cells in rosettes.
These findings suggest an active role of TDC in induction of thymocyte apoptosis, thus mimicking the mechanisms of negative selection [17]. However, an increase in the percentage of apoptotic thymocytes in TDC/thymocyte rosettes may also suggest a role of TDC in preferential binding of apoptotic thymocytes. If this hypothesis that DEC-205 on TDC binds to apoptotic thymocytes is true, based on previously published results on cortical TEC- or CD8+ DC-thymocyte interactions [14, 18], one can expect that anti-DEC-205 mAb inhibits these processes. Our opposite results may suggest that HD83 might increase adhesion of thymocytes to TDC, including apoptotic ones, non-specifically, by modulating binding domains on DEC-205. It is known that mouse and human DEC-205 molecules, showing about 80% homology, are C-type multilectin receptors with a large extracellular portion containing an N-terminal cysteine rich domain, a fibronectin type II domain and 10 domains structurally (although not necessarily functionally) resembling C-type lectin-like domains [5, 7] also known as carbohydrate recognition domains (CRDs). At the moment it is not known whether similar domains are present in rat DEC-205 and which molecules or molecular residues on rat thymocytes, especially on apoptotic cells, bind to these domains. It has been shown only that HD83 mAb binds to an epitope on CRD1 and CRD2 on DEC-205 molecule [8].
It is also possible that HD83, upon binding to DEC-205 on TDC, modulates other adhesion molecules on these cells. Our previous results in the rat system, showed that a number of mAbs, including those to class II MHC molecules and CD45, stimulated the rosette formation between TDC and thymocytes in a LFA-1-dependent and LFA-1-independent pathway, respectively [23].
In conclusion, our results showed that the expression pattern of DEC-205 in the rat thymus is very similar to that in the mouse. In addition, we have addressed for the first time a possible role of rat DEC-205 in thymocyte apoptosis through increased TDC-thymocyte interactions. Although preliminary, these results suggest the involvement of DEC-205 in the processes of thymocyte selection in the thymus. We are grateful to Dr. Chae Gyu Park (Yonsei University College of Medicine, Korea) for a generous gift of HD83 monoclonal antibody.

The authors declare no conflict of interest.
This study is supported by the grants (ON175102) of the Ministry of Education, Science and Technological Development of R. Serbia and the project of the Ministry of Defense of R. Serbia (MFVMA/4/13-15).


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Copyright: © 2014 Polish Society of Experimental and Clinical Immunology This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
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