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Dominique Maciejewski-Lenoir, Jeremy G

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1 Langerhans Cells Release Prostaglandin D2 in Response to Nicotinic Acid 
Dominique Maciejewski-Lenoir, Jeremy G. Richman, Yaron Hakak, Ibragim Gaidarov, Dominic P. Behan, Daniel T. Connolly  Journal of Investigative Dermatology  Volume 126, Issue 12, Pages (December 2006) DOI: /sj.jid Copyright © 2006 The Society for Investigative Dermatology, Inc Terms and Conditions

2 Figure 1 Gene expression levels of GPR109A in human tissues and cell lines. Microarray data for GPR109A were analyzed across a panel of over 100 human samples, a subset of which is shown in Figure 1. Data are the mean±SD. Journal of Investigative Dermatology  , DOI: ( /sj.jid ) Copyright © 2006 The Society for Investigative Dermatology, Inc Terms and Conditions

3 Figure 2 Mouse and human GPR109A distribution in skin. (a) Quantitative RT-PCR analysis of GPR109A mRNA transcripts in dermal or epidermal tissue isolated from mouse ear halves or human skin. (b) Quantitative RT-PCR analysis of mouse GPR109A mRNA transcripts in mouse epidermal cells cultured overnight in RPMI supplemented as indicated. The data are expressed as relative units compared with standard amounts of mouse GPR109A DNA. (c) Western blotting for GPR109A. Rabbit anti-GPR109-COOH polyclonal Ab immunoblotting of lysates (20μg protein/lane) from mouse epidermal cells or HEK293 cells transiently transfected with either GPR109A or plasmid cytomegalovirus. (d–j) Immunostaining of mouse mixed epidermal cells in culture. (d) Fluorescence staining with anti-CD1 Abs (green) and 4′,6 diamidino-2-phenylindole (DAPI) (blue). (e) Fluorescence staining with anti-GPR109-COOH Abs (green) and DAPI (blue). (f) Double fluorescence staining with anti-cytokeratin AE3 Abs (green) and anti-GPR109-COOH Abs (red). (g) Fluorescence staining with anti-GPR109-COOH Abs preincubated with a 10-fold molar excess of antigenic peptide and DAPI. (h) Fluorescence staining with anti-MHC class II 1Ad (green). (i) Fluorescence staining with anti-GPR109-COOH Abs (red). (j) Double fluorescence staining with anti-MHC class II 1Ad (green) and anti-GPR109-COOH Abs (red). Bar=25mm. Journal of Investigative Dermatology  , DOI: ( /sj.jid ) Copyright © 2006 The Society for Investigative Dermatology, Inc Terms and Conditions

4 Figure 3 Immunostaining of cultured CD34+-derived hLCs. (a) Phase contrast micrograph of cells fixed in methanol. (b) Corresponding fluorescence staining with anti-GPR109-COOH Abs. (c–j) Phase contrast and corresponding anti-GPR109-COOH and 4′,6 diamidino-2-phenylindole (DAPI) fluorescence staining of enlarged boxed cells 1 and 2 from (a, b). (g) Fluorescence staining with anti-CD1a Abs and DAPI. (h) Fluorescence staining with anti-langerin Abs. (i) Fluorescence staining with anti-PGD2 synthase Abs. (j, k) Negative control staining with only secondary anti-mouse (j) or anti-rabbit (k) IgG. Bar=10mm Journal of Investigative Dermatology  , DOI: ( /sj.jid ) Copyright © 2006 The Society for Investigative Dermatology, Inc Terms and Conditions

5 Figure 4 IFNγ stimulates GPR109A expression in CD34+-derived hLCs. (a) Quantitative RT-PCR analysis was performed in triplicate using total RNA isolated from hLC-Ls treated overnight with vehicle or IFNγ (75ng/ml). Data represent the ratio of the means of GPR109A mRNA and S9 ribosomal protein mRNA±SE of the mean. (b) Surface expression of GPR109A. hLC-Ls treated with vehicle (blue line) or INFγ (red line) were analyzed by flow cytometry using rabbit anti-GPR109-NH2 polyclonal Ab NLS-179. (c) Immunofluorescence staining of GPR109 on the plasma membrane of hLC-Ls treated with vehicle (left panel) or INFγ (right panel) using rabbit anti-GPR109-NH2 polyclonal Ab NLS-179. Bar=25mm. Journal of Investigative Dermatology  , DOI: ( /sj.jid ) Copyright © 2006 The Society for Investigative Dermatology, Inc Terms and Conditions

6 Figure 5 Nicotinic acid induces PGD2 release in mouse skin ex vivo. Dorsal ear halves were prepared as described and exposed to nicotinic acid for the indicated times. At the end of the incubation, medium was collected for PGD2 determination. Results shown are the mean±SD of quadruplicate determinations from one representative experiment replicated three times with similar results. (a) Dose–response relationship after 45minutes incubation (▪, nicotinic acid; □, nicotinic acid+10μm indomethacin). Data were analyzed using analysis of variance followed by Dunnett's post hoc test: *P<0.05; **P<0.01 when compared with control. (b) Time course (▪, nicotinic acid 1mm; □, Vehicle) *P<0.05, **P<0.01 when compared to all vehicle time points. Journal of Investigative Dermatology  , DOI: ( /sj.jid ) Copyright © 2006 The Society for Investigative Dermatology, Inc Terms and Conditions

7 Figure 6 PGD2 release from CD34+-derived hLCs. Nicotinic acid promotes release of PGD2 in IFNγ-stimulated hLC-Ls. Human LC-Ls were cultured overnight in the presence or absence of 75ng/ml IFNγ, collected, and incubated for 30minutes (25k cells/well) in the presence of increasing concentrations of nicotinic acid±indomethacin. Medium was collected for PGD2 determination. (•, nicotinic acid; ○, nicotinic acid+indomethacin; ▪, nicotinic acid+IFNγ; □, nicotinic acid+IFNγ+indomethacin). Results shown are the mean±SD of triplicate determinations from one representative experiment replicated at least three times with similar results. Analysis of variance followed by Dunnett's post hoc test: **P<0.01 when compared to control. Journal of Investigative Dermatology  , DOI: ( /sj.jid ) Copyright © 2006 The Society for Investigative Dermatology, Inc Terms and Conditions

8 Figure 7 Selectivity of nicotinic acid response. Human LC-Ls were stimulated overnight with 75ng/ml IFNγ, collected, and incubated for 30minutes (25k cells/well) in the presence of indicated compounds. Medium was collected for PGD2 determination. (a) Comparison between nicotinic acid (▪) and Acifran (▴). Open symbols represent corresponding treatments in the presence of indomethacin. Results shown are the mean±SD of triplicate determinations from one representative experiment replicated at least three times with similar results. **P<0.01 when compared to control. (b) Comparison between nicotinic acid (▪) acetic acid (•), and isonicotinic acid (♦). Open symbols represent corresponding treatments in the presence of indomethacin. **P<0.01 when compared to corresponding concentration of other compound. Journal of Investigative Dermatology  , DOI: ( /sj.jid ) Copyright © 2006 The Society for Investigative Dermatology, Inc Terms and Conditions

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