This Article Abstract Full Text (PDF) All Versions of this Article: jhc.7A7308.2007v1 56/3/233    most recent Alert me when this article is cited Alert me if a correction is posted Citation Map Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Verstege, M. I. Articles by te Velde, A. A. Search for Related Content PubMed PubMed Citation Articles by Verstege, M. I. Articles by te Velde, A. A. Social Bookmarking                      What's this?

Dendritic Cell Populations in Colon and Mesenteric Lymph Nodes of Patients With Crohn's Disease

Marleen I. Verstege, Fiebo J.W. ten Kate, Susanne M. Reinartz, Cornelis M. van Drunen, Frederik J.M. Slors, Willem A. Bemelman, Florry A. Vyth-Dreese and Anje A. te Velde

Centre for Experimental and Molecular Medicine (MIV,AAtV), Department of Pathology (FJWtK), Department of Otorhinolaryngology (SMR,CMvD), and Department of Surgery, Academic Medical Centre, Amsterdam, The Netherlands (FJMS,WAB), and Department of Immunology, The Netherlands Cancer Institute, Amsterdam, The Netherlands (FAV-D)

Correspondence to: Marleen I. Verstege, Academic Medical Centre/University of Amsterdam, Centre for Experimental and Molecular Medicine G2-132, PO Box 22700, 1100 DE Amsterdam, The Netherlands. E-mail: m.i.verstege{at}amc.uva.nl

	Summary

Top Summary Introduction Materials and Methods Results Discussion Literature Cited

 
Dendritic cells (DCs) are key cells in innate and adaptive immune responses that determine the pathophysiology of Crohn's disease. Intestinal DCs migrate from the mucosa into mesenteric lymph nodes (MLNs). A number of different markers are described to define the DC populations. In this study we have identified the phenotype and localization of intestinal and MLN DCs in patients with Crohn's disease and non-IBD patients based on these markers. We used immunohistochemistry to demonstrate that all markers (S-100, CD83, DC-SIGN, BDCA1-4, and CD1a) showed a different staining pattern varying from localization in T-cell areas of lymph follicles around blood vessels or single cells in the lamina propria and in the MLN in the medullary cords and in the subcapsular sinuses around blood vessels and in the T-cell areas. In conclusion, all different DC markers give variable staining patterns so there is no marker for the DC. (J Histochem Cytochem 56:233–241, 2008)

Key Words: Crohn's disease • dendritic cell markers • immunohistochemistry

	Introduction

Top Summary Introduction Materials and Methods Results Discussion Literature Cited

 
INFLAMMATORY BOWEL DISEASES (IBD) are chronic inflammatory diseases of the gut leading to Crohn's disease (CD) or ulcerative colitis (UC). The pathogenesis of these diseases is not well understood, but evidence is increasing that dendritic cells (DCs) play an important role in the induction and maintenance of chronic inflammation (Iwasaki 2007; Lee and Iwasaki 2007). DCs of CD patients seem to have an intrinsic abnormal responsiveness to antigens from the lumen of the gut. Mutations in receptors and/or signal transduction molecules may cause altered recognition of antigens such as NOD2 mutations (Hugot et al. 2001; Ogura et al. 2001; Hampe et al. 2002; Netea et al. 2004). However, it is not yet known what DC populations are present in inflamed and control colon and mesenteric lymph nodes (MLNs).

For characterization of human DCs, a series of markers have been used. In peripheral blood, five distinct subsets of DCs have been identified (Table 1 ) (Fithian et al. 1981; Takahashi et al. 1984b; Cochran et al. 1993; Zhou and Tedder 1995; Grouard et al. 1997; Rissoan et al. 1999; Valladeau et al. 1999; Geijtenbeek et al. 2000; Dzionek et al. 2001,2002; Liu et al. 2001; MacDonald et al. 2002). In addition, myeloid and plasmacytoid DCs can be distinguished (Table 1) (Fithian et al. 1981; Takahashi et al. 1984b; Cochran et al. 1993; Zhou and Tedder 1995; Grouard et al. 1997; Rissoan et al. 1999; Valladeau et al. 1999; Geijtenbeek et al. 2000; Dzionek et al. 2001,2002; Liu et al. 2001; MacDonald et al. 2002). Baumgart et al. (2005) demonstrated that, in blood of IBD patients during flare-ups of the disease, immature DCs of both myeloid and plasmacytoid origins are reduced, probably because these cells migrate to the gut.

	Materials and Methods

Top Summary Introduction Materials and Methods Results Discussion Literature Cited

 
Patients and Tissue Samples
Colon and MLNs were obtained with informed consent from patients with CD and non-IBD-related disorders (diverticulitis, polyposis coli, or colon carcinoma) by surgical resection. Non-diseased colon mucosa samples were obtained from patients with colon cancer taken at least 7 cm from the tumor. MLNs that were devoid of cancer metastasis were also obtained from these patients (CD; n=7) and non-IBD-related disorders (n=3). Age range of the CD patients (n=9) was 26–41 years (mean age: 36 years), whereas the age range of patients with non-IBD-related disorders (n=11) was 34–84 years (mean age: 57 years). Prior to the resection procedure, six of the nine CD patients were treated with corticosteroids. After resection, colonic mucosa and MLNs were immediately snap frozen in liquid nitrogen and stored at –80C until cryostat sectioning. Alternatively, samples were fixed in 4% buffered formaldehyde, dehydrated, and embedded in paraffin.

Immunohistochemistry
Frozen Sections
BDCA-1-4 Staining
Serial cryostat sections were cut on a Cryo-Star HM560 (Microm; Walldorf, Germany) and transferred to aminopropyltriethoxysilane (APES)-coated glass slides (StarFrost; Knittel, Klinipath, Duiven, The Netherlands), dried, and stored at –80C until further processing. Tissue sections were defrosted at room temperature, dried, and fixed in ice-cold acetone for 10 min at room temperature. After fixation, tissue sections were rinsed with PBS (pH 7.8), placed in a semi-automatic stainer (Sequenza; Shandon, Breda, The Netherlands), and incubated with normal goat serum (CLB; Amsterdam, The Netherlands) to block nonspecific staining for 10 min. Sections were then incubated with primary antibody for 60 min at room temperature. Mouse anti-human monoclonal antibodies (Miltenyi Biotec; Bergisch Gladbach, Germany) directed against BDCA-1 (AD5-8E7), BDCA-2 (AC144), BDCA-3 (AD5-14H12), and BDCA-4 (AD5-17F6) were used. All primary antibodies were diluted in PBS containing 1% blocking reagent (10,961,760; Roche Diagnostics GmbH, Mannheim, Germany) to block endogenous avidin and biotin activity. Following incubation with primary antibody, sections were rinsed with PBS for 5 min and incubated with biotinylated goat anti-mouse antiserum (Biogenics; Klinipath) for 30 min at room temperature. Next, sections were rinsed with PBS and incubated with streptavidin alkaline phosphatase (ss-AP; Biogenics, Klinipath) for 30 min at room temperature. Sections were then rinsed with PBS containing Tris buffer (0.2 mol/liter, pH 8.5) and incubated with New Fuchsin (Chroma; Kongen, Germany) substrate (containing levamisole to block endogenous AP enzyme activity) for 20 min at room temperature. Sections were counterstained with Gill's hematoxylin, rinsed with distilled water, and mounted in Vecta Mount (Vector Laboratories; Burlingame, CA). Control staining was performed by substituting primary antibody with an isotypic control monoclonal antibody.

DC-SIGN and CD83 Staining
Frozen sections were stained using a standard alkaline phosphatase protocol as described previously (te Velde et al. 2003). In short, sections were incubated in 5% (v/v) normal goat serum (CLB) to block nonspecific staining for 10 min. Sections were then stained with either anti-CD83 as primary MAb (Beckman Coulter; Mijdrecht, The Netherlands) or with FITC-labeled anti-DC-SIGN (obtained from Dr. Y. van Kooyk; Free University Medical Center, Amsterdam, The Netherlands). Following incubation with primary antibody, sections were extensively rinsed in PBS and incubated with biotinylated goat anti-mouse IgG (Dako; Glostrup, Denmark). Next, FITC-labeled MAb sections were incubated with rabbit anti-FITC antibody (Dako) and goat anti-rabbit antibody (Dako). Subsequently, sections were incubated with streptavidin/biotin-conjugated alkaline phosphatase complex (ABC protocol; Dako). Color was developed using as substrate naphthol AS-MX phosphate (0.3 mg/ml) plus New Fuchsin (0.1 mg/ml; Chroma) in 0.2 M Tris–HCl buffer, pH 8.0 (ABC protocol), and sections were counterstained with hematoxylin.

Paraffin Sections
Paraffin sections were stretched and dried at 37C overnight, deparaffinized in xylene, and rehydrated in alcohol series. To block endogenous peroxidase activity, sections were treated with 3% H₂O₂ in methanol for 20 min. Sections were subjected to heat-induced epitope retrieval for 10 min at 95C. To block nonspecific binding sites, sections were incubated with normal goat serum (5% in PBS) for 10 min. Sections were then incubated with primary antibodies CD1a (1:20; Dako) and S-100 (1:4000; Dako) diluted in PBS containing 5% BSA for 1 hr. After incubation with secondary antibodies (Dako), peroxidase activity was demonstrated by using 3,3-diaminobenzidine tetrachloride (Sigma; St Louis, MO). Finally, sections were counterstained with hematoxylin, dehydrated, and mounted in Pertex (Sigma–Aldrich; Steinheim, Germany).

All sections were examined in a double-blind manner by a pathologist.

	Results

Top Summary Introduction Materials and Methods Results Discussion Literature Cited

 
Myeloid DCs
Distribution patterns of myeloid DCs in colonic mucosa and MLNs of non-CD and CD patients using the DC markers BDCA1, BDCA3, S-100, DC-SIGN, CD83, and CD1a are summarized in Table 3 .

View larger version (143K): [in this window] [in a new window]   Figure 1 Photographs of the immunohistochemical determination of the expression of the myeloid dendritic cell (DC) markers BDCA1 (A,B) and BDCA3 (C,D) in colonic tissue (A,C) and mesenteric lymph nodes (MLNs) (B,D) from Crohn's disease (CD) patients. Insets in B and D indicate the localization of the staining in MLN. Bar = 100 µm.

View larger version (156K): [in this window] [in a new window]   Figure 2 Photographs of the immunohistochemical localization of S-100 expression in colon (A,C) and MLN (B,D) of non-CD (A,B) and CD patients (C,D). Insets in B and D indicate localization of staining in MLN. Bar = 100 µm.

View larger version (80K): [in this window] [in a new window]   Figure 3 Photographs of the immunohistochemical localization of DC-SIGN (A) and CD83 (B) expression in the MLN of CD patients. Insets indicate the localization of staining in MLN. Bar = 100 µm.

Plasmacytoid DCs
Plasmacytoid DCs are characterized by the expression of BDCA2 and BDCA4. BDCA2 expression of a few cells was found in lymph follicles in colon, whereas BDCA2⁺ cells were absent in mucosa of both non-CD and CD patients (Figure 4 ). In contrast, expression of BDCA4 was strong in endothelial cells in LP of both non-CD and CD patients. In MLN, expression of both BDCA2 and BDCA4 was closely associated with high endothelial venules (HEVs).

View larger version (143K): [in this window] [in a new window]   Figure 4 Photographs of the immunohistochemical localization of expression of the plasmacytoid DC markers BDCA2 (A,B) and BDCA4 (C,D) in colonic tissue (A,C) and MLNs (B,D) of CD patients. Inset in A indicates the presence of BDCA2+ cells in follicles in the wall of the colon. Insets in B and D indicate localization of staining in MLN. Bars: A–D = 100 µm; Inset in A = 200 µm.

	Discussion

Top Summary Introduction Materials and Methods Results Discussion Literature Cited

In general, LNs contain three types of DCs, i.e., interdigitating DCs (IDCs), follicular DCs, and plasmacytoid DCs. IDCs are like Langerhans cells characterized by the expression of S-100, which is a member of the family of calcium-binding proteins (Takahashi et al. 1984a,b; Cochran et al. 1993). Based on the localization of markers, we demonstrated that S-100⁺ and also CD83⁺ cells present in the MLN are most likely IDCs, which are mature DCs from myeloid origin and capable of presenting antigens to naive T cells in the paracortical areas. Moreover, in colonic tissue, S-100 as well as CD83 demonstrated a similar expression pattern in lymph aggregates, suggesting that they are involved in similar functional processes. In contrast, S-100 expression in cervical LNs was absent in lymph follicles (Takahashi et al. 2001; Engering et al. 2004). Furthermore, only subcapsular sinuses of CD patients and not of non-CD patients harbor S-100⁺ DCs, indicating that in CD patients there is an increased influx of mature DCs of MLNs via subcapsular sinuses into the T-cell areas. An increased number of S-100⁺ DCs was also found in extrafollicular T-cell areas in hyperplastic palatine tonsils of patients with tonsillitis (Papadas et al. 2001), in several autoimmune diseases such as juvenile rheumatoid arthritis (Frosch et al. 2003), and in primary biliary cirrhosis (Demetris et al. 1989), confirming a role for S-100⁺ cells in inflammatory processes. Moreover, S-100 is expressed by nerve cells and cancer cells and is used as a marker in cases of melanoma, nerve tissue cancer, and several carcinomas (Takahashi et al. 1984a; Daimaru et al. 1985; Monda and Wick 1985; Drier et al. 1987; Wick et al. 1988; Gillett et al. 1990; Cochran et al. 1993).

BDCA3⁺ cells are likely to be IDCs, but because of their specific localization at the border of lymph follicles and sinuses they seem to belong to a myeloid cell type other than S-100⁺ and CD83⁺ DCs. These cells may be capable of interacting with B and T cells to induce humeral responses. However, BDCA3⁺ cells may be more involved in antigen-capturing processes because they are found in LP.

Follicular DCs are characterized by none of the described markers. Expression of BDCA1 in the mantle zone of B-cell follicles may be indicative of follicular DCs; however, expression is not restricted to DCs. B-cell subsets in the germinal center and mantle zone of LNs, marginal zone B cells in the spleen, and a subpopulation of B cells in the peripheral blood also express BDCA1 (Small et al. 1987; Smith et al. 1988; Plebani et al. 1993), which belongs to a family of lipid antigen-presenting molecules (Brigl and Brenner 2004). The observation that BDCA1⁺ cells were smaller and without the characteristic morphology of DCs suggests that expression of BDCA1 in MLN is due to the presence of B cells rather than DCs.

DC-SIGN is a C-type lectin involved in sampling antigens by recognition of specific carbohydrate structures of autoantigens and foreign antigens and is therefore mainly expressed by immature DCs and macrophages (Geijtenbeek et al. 2000). This is consistent with our earlier findings that DC-SIGN⁺ cells are scattered throughout colonic mucosa where these cells can encounter antigens. DC-SIGN⁺ cells were present in medullary cords of MLNs, but in contrast to cervical LNs no expression was detected in the outer zone of the paracortex (Engering et al. 2004).

Although CD1a is mainly used as a marker for Langerhans cells in the skin, expression of this marker is not restricted to this cell type because subsets of interstitial and monocyte-derived DCs also express CD1a (Tazi et al. 1993; Zhou and Tedder 1996; Yoshida et al. 1997). However, CD1a was not detectable in MLNs and colonic tissue of both non-CD and CD patients. Moreover, subsets of DCs in the superficial LNs were CD1a positive, whereas CD1a expression is absent in deeply located LNs including mesenteric, mediastinal, and para-aortic LNs (Takahashi et al. 2001). Additionally, expression of CD1a does not occur in inguinal and liver LNs (Tanis et al. 2004).

Expression of plasmacytoid DC marker BDCA2 has been observed in close association with HEVs, indicating that tissue plasmacytoid DC precursors are blood-derived cells that enter MLN in the HEVs. In agreement with these results, Yoneyama et al. (2004) demonstrated that myeloid DCs migrate via lymph vessels into draining LNs, whereas plasmacytoid DCs enter LNs via the HEVs. BDCA2⁺ DCs seem to be mainly involved in antigen-capturing processes, and BDCA2 is a C-type lectin transmembrane glycoprotein that internalizes antigens to present to T cells (Dzionek et al. 2001). BDCA2 expression was absent in colonic mucosa of both non-CD and CD patients, which coincides with the results of Middel et al. (2006). BDCA4 is a neuronal receptor of the class 3 semaphorin family and is also expressed by endothelial cells to function as a coreceptor for vascular endothelial growth factor A (Dzionek et al. 2002). This suggests that BDCA4 expression at HEVs and in the LP is related to endothelial cells instead of DCs.

In the current study we have shown that different DC markers give variable staining patterns so that there is no marker for DCs. These different ‘DC markers’ are present in different sites in the colon and MLN in CD patients, indicating that DCs are a heterogeneous group of antigen-presenting cells harboring different functions. Our data indicate that colonic tissue and MLNs harbor at least three different myeloid DC populations. One population consists of immature DCs, which express DC-SIGN and are mainly located at antigen-capturing sites in the mucosa and medullary cords. A second population of DCs expresses BDCA3 and, similar to DC-SIGN⁺ DCs, also presents as single cells in the mucosa, suggesting that BDCA3⁺ DCs may be involved in antigen-capturing processes. In the MLN, their location around the lymph follicles suggests a role in the activation of B and T cells. The third DC population consists of mature DCs that express S-100 and CD83. Their location in the T-cell areas in both the colonic lymph follicles as well as the MLN suggests that they have the capacity to present antigen to T cells. DCs from plasmacytoid origin were hardly present in the colon and MLN. Although BDCA4 expression was found around the blood vessels, its expression is probably on endothelial cells instead of DCs.

Future studies will involve the isolation of the described different DC populations for further investigation to utilize favorable results for the development of new therapeutic strategies in the treatment of CD.

	Acknowledgments

 
We thank Esther de Groot and Trees Dellemijn for performing immunohistochemical staining and Kate Cameron for carefully reading the manuscript.

	Footnotes

 
Received for publication July 6, 2007; accepted November 4, 2007

	Literature Cited

Top Summary Introduction Materials and Methods Results Discussion Literature Cited

 

Baumgart DC, Metzke D, Schmitz J, Scheffold A, Sturm A, Wiedenmann B, Dignass AU (2005) Patients with active inflammatory bowel disease lack immature peripheral blood plasmacytoid and myeloid dendritic cells. Gut 54:228–236[Abstract/Free Full Text]

Brigl M, Brenner MB (2004) CD1: antigen presentation and T cell function. Annu Rev Immunol 22:817–890[CrossRef][Medline]

Cambi A, Koopman M, Figdor CG (2005) How C-type lectins detect pathogens. Cell Microbiol 7:481–488[CrossRef][Medline]

Cochran AJ, Lu HF, Li PX, Saxton R, Wen DR (1993) S-100 protein remains a practical marker for melanocytic and other tumours. Melanoma Res 3:325–330[Medline]

Daimaru Y, Hashimoto H, Enjoji M (1985) Malignant peripheral nerve-sheath tumors (malignant schwannomas). An immunohistochemical study of 29 cases. Am J Surg Pathol 9:434–444[Medline]

Demetris AJ, Sever C, Kakizoe S, Oguma S, Starzl TE, Jaffe R (1989) S100 protein positive dendritic cells in primary biliary cirrhosis and other chronic inflammatory liver diseases. Relevance to pathogenesis? Am J Pathol 134:741–747[Abstract]

Drier JK, Swanson PE, Cherwitz DL, Wick MR (1987) S100 protein immunoreactivity in poorly differentiated carcinomas. Immunohistochemical comparison with malignant melanoma. Arch Pathol Lab Med 111:447–452[Medline]

Dzionek A, Inagaki Y, Okawa K, Nagafune J, Rock J, Sohma Y, Winkels G, et al. (2002) Plasmacytoid dendritic cells: from specific surface markers to specific cellular functions. Hum Immunol 63:1133–1148[CrossRef][Medline]

Dzionek A, Sohma Y, Nagafune J, Cella M, Colonna M, Facchetti F, Gunther G, et al. (2001) BDCA-2, a novel plasmacytoid dendritic cell-specific type II C-type lectin, mediates antigen capture and is a potent inhibitor of interferon /β induction. J Exp Med 194:1823–1834[Abstract/Free Full Text]

Engering A, van Vliet SJ, Hebeda K, Jackson DG, Prevo R, Singh SK, Geijtenbeek TB, et al. (2004) Dynamic populations of dendritic cell-specific ICAM-3 grabbing nonintegrin-positive immature dendritic cells and liver/lymph node-specific ICAM-3 grabbing nonintegrin-positive endothelial cells in the outer zones of the paracortex of human lymph nodes. Am J Pathol 164:1587–1595[Abstract/Free Full Text]

Fithian E, Kung P, Goldstein G, Rubenfeld M, Fenoglio C, Edelson R (1981) Reactivity of Langerhans cells with hybridoma antibody. Proc Natl Acad Sci USA 78:2541–2544[Abstract/Free Full Text]

Frosch M, Vogl T, Seeliger S, Wulffraat N, Kuis W, Viemann D, Foell D, et al. (2003) Expression of myeloid-related proteins 8 and 14 in systemic-onset juvenile rheumatoid arthritis. Arthritis Rheum 48:2622–2626[CrossRef][Medline]

Geijtenbeek TB, Torensma R, van Vliet SJ, van Duijnhoven GC, Adema GJ, van Kooyk Y, Figdor CG (2000) Identification of DC-SIGN, a novel dendritic cell-specific ICAM-3 receptor that supports primary immune responses. Cell 100:575–585[CrossRef][Medline]

Gillett CE, Bobrow LG, Millis RR (1990) S100 protein in human mammary tissue immunoreactivity in breast carcinoma, including Paget's disease of the nipple, and value as a marker of myoepithelial cells. J Pathol 160:19–24[CrossRef][Medline]

Grouard G, Rissoan MC, Filgueira L, Durand I, Banchereau J, Liu YJ (1997) The enigmatic plasmacytoid T cells develop into dendritic cells with interleukin (IL)-3 and CD40-ligand. J Exp Med 185:1101–1111[Abstract/Free Full Text]

Hampe J, Grebe J, Nikolaus S, Solberg C, Croucher PJ, Mascheretti S, Jahnsen J, et al. (2002) Association of NOD2 (CARD 15) genotype with clinical course of Crohn's disease: a cohort study. Lancet 359:1661–1665[CrossRef][Medline]

Hugot JP, Chamaillard M, Zouali H, Lesage S, Cezard JP, Belaiche J, Almer S, et al. (2001) Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. Nature 411:599–603[CrossRef][Medline]

Iwasaki A (2007) Mucosal dendritic cells. Annu Rev Immunol 25:381–418[CrossRef][Medline]

Jullien D, Stenger S, Ernst WA, Modlin RL (1997) CD1 presentation of microbial nonpeptide antigens to T cells. J Clin Invest 99:2071–2074[Medline]

Lee HK, Iwasaki A (2007) Innate control of adaptive immunity: dendritic cells and beyond. Semin Immunol 19:48–55[CrossRef][Medline]

Liu YJ, Kanzler H, Soumelis V, Gilliet M (2001) Dendritic cell lineage, plasticity and cross-regulation. Nat Immunol 2:585–589[CrossRef][Medline]

MacDonald KP, Munster DJ, Clark GJ, Dzionek A, Schmitz J, Hart DN (2002) Characterization of human blood dendritic cell subsets. Blood 100:4512–4520[Abstract/Free Full Text]

Middel P, Raddatz D, Gunawan B, Haller F, Radzun HJ (2006) Increased number of mature dendritic cells in Crohn's disease: evidence for a chemokine mediated retention mechanism. Gut 55:220–227[Abstract/Free Full Text]

Monda L, Wick MR (1985) S-100 protein immunostaining in the differential diagnosis of chondroblastoma. Hum Pathol 16:287–293[CrossRef][Medline]

Netea MG, Kullberg BJ, de Jong DJ, Franke B, Sprong T, Naber TH, Drenth JP, et al. (2004) NOD2 mediates anti-inflammatory signals induced by TLR2 ligands: implications for Crohn's disease. Eur J Immunol 34:2052–2059[CrossRef][Medline]

Ogura Y, Bonen DK, Inohara N, Nicolae DL, Chen FF, Ramos R, Britton H, et al. (2001) A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. Nature 411:603–606[CrossRef][Medline]

Papadas T, Batistatou A, Ravazoula P, Zolota V, Goumas P (2001) S-100 protein-positive dendritic cells and CD34-positive dendritic interstitial cells in palatine tonsils. Eur Arch Otorhinolaryngol 258:243–245[CrossRef][Medline]

Plebani A, Proserpio AR, Guarneri D, Buscaglia M, Cattoretti G (1993) B and T lymphocyte subsets in fetal and cord blood: age-related modulation of CD1c expression. Biol Neonate 63:1–7[Medline]

Rissoan MC, Soumelis V, Kadowaki N, Grouard G, Briere F, de Waal MR, Liu YJ (1999) Reciprocal control of T helper cell and dendritic cell differentiation. Science 283:1183–1186[Abstract/Free Full Text]

Sadler JE (1997) Thrombomodulin structure and function. Thromb Haemost 78:392–395[Medline]

Small TN, Knowles RW, Keever C, Kernan NA, Collins N, O'Reilly RJ, Dupont B, et al. (1987) M241 (CD1) expression on B lymphocytes. J Immunol 138:2864–2868[Abstract]

Smith ME, Thomas JA, Bodmer WF (1988) CD1c antigens are present in normal and neoplastic B-cells. J Pathol 156:169–177[CrossRef][Medline]

Takahashi K, Isobe T, Ohtsuki Y, Akagi T, Sonobe H, Okuyama T (1984a) Immunohistochemical study on the distribution of alpha and beta subunits of S-100 protein in human neoplasm and normal tissues. Virchows Arch B Cell Pathol Incl Mol Pathol 45:385–396[Medline]

Takahashi K, Isobe T, Ohtsuki Y, Sonobe H, Takeda I, Akagi T (1984b) Immunohistochemical localization and distribution of S-100 proteins in the human lymphoreticular system. Am J Pathol 116:497–503[Abstract]

Takahashi K, Kenji A, Norihiro T, Eisaku K, Takashi O, Kazuhiko H, Tadashi Y, et al. (2001) Morphological interactions of interdigitating dendritic cells with B and T cells in human mesenteric lymph nodes. Am J Pathol 159:131–138[Abstract/Free Full Text]

Tanis W, Mancham S, Binda R, Janssen HL, Bezemer G, IJzermans JN, Tilanus HW, et al. (2004) Human hepatic lymph nodes contain normal numbers of mature myeloid dendritic cells but few plasmacytoid dendritic cells. Clin Immunol 110:81–88[CrossRef][Medline]

Tazi A, Bouchonnet F, Grandsaigne M, Boumsell L, Hance AJ, Soler P (1993) Evidence that granulocyte macrophage-colony-stimulating factor regulates the distribution and differentiated state of dendritic cells/Langerhans cells in human lung and lung cancers. J Clin Invest 91:566–576[Medline]

te Velde AA, van Kooyk Y, Braat H, Hommes DW, Dellemijn TA, Slors JF, van Deventer SJ, et al. (2003) Increased expression of DC-SIGN+IL-12+IL-18+ and CD83+IL-12-IL-18- dendritic cell populations in the colonic mucosa of patients with Crohn's disease. Eur J Immunol 33:143–151[CrossRef][Medline]

Valladeau J, Duvert-Frances V, Pin JJ, Dezutter-Dambuyant C, Vincent C, Massacrier C, Vincent J, et al. (1999) The monoclonal antibody DCGM4 recognizes Langerin, a protein specific of Langerhans cells, and is rapidly internalized from the cell surface. Eur J Immunol 29:2695–2704[CrossRef][Medline]

Wick MR, Swanson PE, Rocamora A (1988) Recognition of malignant melanoma by monoclonal antibody HMB-45. An immunohistochemical study of 200 paraffin-embedded cutaneous tumors. J Cutan Pathol 15:201–207[CrossRef][Medline]

Yoneyama H, Matsuno K, Zhang Y, Nishiwaki T, Kitabatake M, Ueha S, Narumi S, et al. (2004) Evidence for recruitment of plasmacytoid dendritic cell precursors to inflamed lymph nodes through high endothelial venules. Int Immunol 16:915–928[Abstract/Free Full Text]

Yoshida A, Imayama S, Sugai S, Kawano Y, Ishibashi T (1997) Increased number of IgE positive Langerhans cells in the conjunctiva of patients with atopic dermatitis. Br J Ophthalmol 81:402–406[Abstract/Free Full Text]

Zhou LJ, Tedder TF (1995) Human blood dendritic cells selectively express CD83, a member of the immunoglobulin superfamily. J Immunol 154:3821–3835[Abstract]

Zhou LJ, Tedder TF (1996) CD14+ blood monocytes can differentiate into functionally mature CD83+ dendritic cells. Proc Natl Acad Sci USA 93:2588–2592[Abstract/Free Full Text]

CiteULike    Complore    Connotea    Del.icio.us    Digg    Reddit    Technorati    What's this?

This article has been cited by other articles:

				C. E. Angel, C.-J. J. Chen, O. C. Horlacher, S. Winkler, T. John, J. Browning, D. MacGregor, J. Cebon, and P. R. Dunbar Distinctive localization of antigen-presenting cells in human lymph nodes Blood, February 5, 2009; 113(6): 1257 - 1267. [Abstract] [Full Text] [PDF]

				M. Chichlowski and L. P. Hale Bacterial-mucosal interactions in inflammatory bowel disease--an alliance gone bad Am J Physiol Gastrointest Liver Physiol, December 1, 2008; 295(6): G1139 - G1149. [Abstract] [Full Text] [PDF]

This Article Abstract Full Text (PDF) All Versions of this Article: jhc.7A7308.2007v1 56/3/233    most recent Alert me when this article is cited Alert me if a correction is posted Citation Map Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Verstege, M. I. Articles by te Velde, A. A. Search for Related Content PubMed PubMed Citation Articles by Verstege, M. I. Articles by te Velde, A. A. Social Bookmarking                      What's this?

Guidelines | Subscriptions | About | exPRESS - Current - Archive | Business Information | Contact