Research Paper
Maturation and upregulation of functions of murine dendritic cells (DCs) under the influence of purified Aromatic-Turmerone (AR)
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Volume 8, Issue 10 October 2012
Pages 1416 - 1424
http://dx.doi.org/10.4161/hv.21526
Keywords: AR, BMDCs, maturation, modulation
Authors: Tan Yonggang, Meng Yiming, Zhang Heying, Sun Cheng, Wang Qiushi, Yang Xianghong, Zheng Wei, Zhou Huawei and Fengping Shan
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- Tan Yonggang
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Corresponding author: fpshan@mail.cmu.edu.cn
Department of Oncology; Shengjing Hospital; China Medical University; Heping District, Shenyang, P.R. China
- Meng Yiming
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Department of Immunology; School of Basic Medical Science; China Medical University; Heping District, Shenyang, P.R. China
- Zhang Heying
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Department of Oncology; Shengjing Hospital; China Medical University; Heping District, Shenyang, P.R. China
- Sun Cheng
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Department of Oncology; Shengjing Hospital; China Medical University; Heping District, Shenyang, P.R. China
- Wang Qiushi
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Department of Oncology; Shengjing Hospital; China Medical University; Heping District, Shenyang, P.R. China
- Yang Xianghong
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Department of Oncology; Shengjing Hospital; China Medical University; Heping District, Shenyang, P.R. China
- Zheng Wei
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Department of Oncology; Shengjing Hospital; China Medical University; Heping District, Shenyang, P.R. China
- Zhou Huawei
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Department of Oncology; Shengjing Hospital; China Medical University; Heping District, Shenyang, P.R. China
- Fengping Shan
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Department of Immunology; School of Basic Medical Science; China Medical University; Heping District, Shenyang, P.R. China; Institute of pathology and pathophysiology; School of Basic Medical Science; China Medical University; Heping District, Shenyang, P.R. China
Abstract:
The aim of this work is to evaluate the effects of purified aromatic-turmerone(ar-turmerione, AR) on murine dendritic cells (DCs). These impacts of AR on DCs from bone marrow derived DCs(BMDCs) were assessed with use of conventional scanning electron microscopy (SEM), fluorescence activated cell sorting (FACS), transmission electron microscopy (TEM), cytochemistry assay, FITC-dextran, bio-assay and enzyme linked immunosorbent assay (ELISA). We found that AR induced phenotypic maturation as evidenced by increased expression of CD86, CD40, CD83, CD80 and major histocompatibility complex II (MHC II). The functional tests showed the activity of acidic phosphatase (ACP) inside the DCs were downregulated after treatment with AR (which occurs when phagocytosis of DCs were decreased). Finally, we proved that AR increased the production of IL-12 and tumor necrosis factor α (TNF-α). These data suggested that AR could promote phenotypic and functional maturation of DCs and this adjuvant-like activity may have potential therapeutic value. It is therefore concluded that AR could exert positive modulation on murine DCs.
Received: May 29, 2012; Accepted: July 18, 2012; Published Online: October 1, 2012
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