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Low Concentrations of Curcumin Induce Growth Arrest and Apoptosis in Skin Keratinocytes Only in Combination with UVA or Visible Light  Jadranka Dujic,

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Presentation on theme: "Low Concentrations of Curcumin Induce Growth Arrest and Apoptosis in Skin Keratinocytes Only in Combination with UVA or Visible Light  Jadranka Dujic,"— Presentation transcript:

1 Low Concentrations of Curcumin Induce Growth Arrest and Apoptosis in Skin Keratinocytes Only in Combination with UVA or Visible Light  Jadranka Dujic, Stefan Kippenberger, Stephanie Hoffmann, Ana Ramirez-Bosca, Jaime Miquel, Joquin Diaz-Alperi, Jürgen Bereiter- Hahn, Roland Kaufmann, August Bernd  Journal of Investigative Dermatology  Volume 127, Issue 8, Pages (August 2007) DOI: /sj.jid Copyright © 2007 The Society for Investigative Dermatology, Inc Terms and Conditions

2 Figure 1 Cellular uptake and intracellular distribution of curcumin. HaCaT cells were incubated with 5μg/ml curcumin. (a) The uptake was determined by measuring the optical density of methanolic cell extracts after 0–6hours. Each value represents the mean of three independent experiments. (b) The fluorescent distribution is shown by confocal laser-scanning microscopy after 40minutes. Bar=5μm. Experiments were repeated with similar results. Journal of Investigative Dermatology  , DOI: ( /sj.jid ) Copyright © 2007 The Society for Investigative Dermatology, Inc Terms and Conditions

3 Figure 2 Curcumin combined with UVA or visible light inhibits cell proliferation. (a) HaCaT cells and (b) primary kerationcytes were preincubated with curcumin and irradiated in the presence of curcumin as described in Materials and Methods with 1J/cm2 UVA (▾), or 5,500lx visible light (5minutes) (•), or kept light protected (□). BrdU incorporation was determined after 24hours. The values of the control were set to 100%. Each bar represents the mean of five independent experiments (*P<0.005 vs untreated control). The experiment was repeated with similar results. Journal of Investigative Dermatology  , DOI: ( /sj.jid ) Copyright © 2007 The Society for Investigative Dermatology, Inc Terms and Conditions

4 Figure 3 Curcumin combined with UVA does not induce ROS. HaCaT cells were preincubated with dihydrorhodamine and (a) curcumin or (b) psoralen as described in Materials and Methods and then irradiated with 20J/cm2 UVA (black bars) or kept light protected (white bars). Data measured after 90minutes are shown. (c) HaCaT cells were irradiated with 0.5–20J/cm2 and rhodamine 123 fluorescence was determined as described above. The values of the control were set to 100%. Each bar represents the mean of eight independent experiments (*P<0.005 vs (a), (b) irradiated or c untreated control). Experiments were repeated with similar results. Journal of Investigative Dermatology  , DOI: ( /sj.jid ) Copyright © 2007 The Society for Investigative Dermatology, Inc Terms and Conditions

5 Figure 4 Curcumin combined with UVA does not induce toxic membrane damage. HaCaT cells were preincubated with curcumin and irradiated in the presence of curcumin as described in Materials and Methods with 1J/cm2 UVA (black bars) or kept light protected (white bars). After 24hours, lactate dehydrogenase (LDH) of the cell-free supernatants was measured. Supernatants of cells treated with 1% Triton X100 (gray bars) served as a positive control. Each bar represents the mean of three independent experiments. The experiment was repeated with similar results. Journal of Investigative Dermatology  , DOI: ( /sj.jid ) Copyright © 2007 The Society for Investigative Dermatology, Inc Terms and Conditions

6 Figure 5 Curcumin combined with UVA induces apoptotic bodies. HaCaT cells were preincubated with curcumin, then (a) kept light protected or (b) were irradiated with 1J/cm2 UVA. After 24hours, bisbenzimide staining was performed. Apoptotic bodies are marked with arrows. (c) The evaluation was carried out by counting approximately 200 cells of each probe of irradiated (black bars), or light protected (white bars) as well as 1μM staurosporine-treated cells (positive control; gray bar) (*P<0.05 vs untreated control). Bar=10μm. The experiment was repeated with similar results. Journal of Investigative Dermatology  , DOI: ( /sj.jid ) Copyright © 2007 The Society for Investigative Dermatology, Inc Terms and Conditions

7 Figure 6 Curcumin combined with UVA or visible light enhances the release of cytochrome c. HaCaT cells were preincubated with curcumin and irradiated in the presence of curcumin as described in Materials and Methods with 1J/cm2 UVA (gray bars), or 5,500lx visible light (5minutes) (black bars) or kept light protected (white bars). The positive control was incubated with 1μM Staurosporine (striped bar). After 24hours, cytoplasmic extracts were obtained and cytochrome c determination was performed. The values of the control were set to 100%. Each bar represents the mean of three independent experiments (*P<0.05 vs untreated control). The experiment was repeated with similar results. Journal of Investigative Dermatology  , DOI: ( /sj.jid ) Copyright © 2007 The Society for Investigative Dermatology, Inc Terms and Conditions

8 Figure 7 Curcumin combined with UVA activates caspases. HaCaT cells were preincubated with curcumin and irradiated in the presence of curcumin as described in Materials and Methods with 1J/cm2 UVA (lanes 4–6) or kept light protected (lanes 1–3). After 1.5 and 2hours, proteins were obtained and Western blotting was performed. The blots show the inactive procaspases and the cleaved forms (black arrows) of (left panel) caspase-9 and (right panel) caspase-8. The experiment was repeated with similar results. Journal of Investigative Dermatology  , DOI: ( /sj.jid ) Copyright © 2007 The Society for Investigative Dermatology, Inc Terms and Conditions

9 Figure 8 Curcumin combined with UVA or visible light inhibits NF-κB. (a) HaCaT cells were cotransfected with NF-κB-binding domain promoter as well as with an SV40 promotor plasmid. The next day, cells were preincubated with curcumin and irradiated in the presence of curcumin as described in Materials and Methods with 1J/cm2 UVA (gray bars), or 5,500lx visible light (5min) (black bars) or kept light protected (white bars). The positive control was incubated with 20ng/ml TNF-α (striped bar). After 24hours, cell lysates were obtained and NF-κB transactivation assay was performed. The values of the control were set to 100%. Each bar represents the mean of four independent experiments (*P<0.05 vs untreated control). The experiment was repeated with similar results. (b and c) HaCaT cells were treated with curcumin and UVA as described above. After the addition of 10ng/ml TNF-α for 30minutes, nuclear and cytosolic proteins were extracted. (b) Electrophoretic mobility shift assay was carried out with nuclear extracts of curcumin-treated (lanes 1–4) and curcumin/UVA-treated (lanes 5–8) HaCaT cells and 32P-labeled NF-κB consensus sequence. Competition (C) and supershift using a specific NFκB antibody (S) were performed as described in Materials and Methods. (c) Amounts of nuclear NFκB (p65) were detected by Western blot analysis. As loading control served Sp1. Cytosolic extracts of the same samples were used for detection of IκB-α. As loading control served β-actin. Experiments were repeated with similar results. Journal of Investigative Dermatology  , DOI: ( /sj.jid ) Copyright © 2007 The Society for Investigative Dermatology, Inc Terms and Conditions

10 Figure 9 Curcumin combined with UVA inhibits PKB/Akt, ERK1/2, and EGF-R. HaCaT cells were preincubated with curcumin and irradiated in the presence of curcumin as described in Materials and Methods with 1J/cm2 UVA (lanes 4–6) or kept light protected (lanes 1–3). Then 100ng/ml TGF-α was added to the cells. After 15minutes, proteins were obtained and Western blotting was performed with antibodies directed toward (a) phosho-PKB/Akt (Ser), phospho-PKB/Akt (Thr), PKB/Akt, (b) phospho-ERK1/2, ERK1/2, and (c) phospho-EGF-R. Detection of total PKB/Akt and ERK1/2 served as loading control. The experiment was repeated with similar results. Journal of Investigative Dermatology  , DOI: ( /sj.jid ) Copyright © 2007 The Society for Investigative Dermatology, Inc Terms and Conditions

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