1. Academic Validation
  2. CCL-34, a synthetic toll-like receptor 4 activator, modulates differentiation and maturation of myeloid dendritic cells

CCL-34, a synthetic toll-like receptor 4 activator, modulates differentiation and maturation of myeloid dendritic cells

  • Oncotarget. 2016 Mar 8;7(10):11677-86. doi: 10.18632/oncotarget.7315.
Shu-Ling Fu 1 Chun-Cheng Lin 2 Ming-Ling Hsu 3 Sheng-Hung Liu 1 Yu-Chuen Huang 4 Yu-Jen Chen 1 3 5
Affiliations

Affiliations

  • 1 Institute of Traditional Medicine, National Yang-Ming University, Taipei, Taiwan.
  • 2 Department of Chemistry, National Tsing Hua University, Hsinchu, Taiwan.
  • 3 Department of Medical Research, MacKay Memorial Hospital, Taipei, Taiwan.
  • 4 School of Chinese Medicine, College of Chinese Medicine, China Medical University, Taichung, Taiwan.
  • 5 Department of Radiation Oncology, MacKay Memorial Hospital, Taipei, Taiwan.
Abstract

CCL-34, a synthetic α-galactosylceramide analog, has been reported as an activator of Toll-like Receptor 4 (TLR4) in macrophages. TLR4 is highly expressed in dendritic cell (DC) and several TLR4 agonists are known to trigger DC maturation. We herein evaluated the effect of CCL-34 on DC maturation. Human CD14+ monocyte-derived immature DC were treated with CCL-34, its inactive structural analog CCL-44, or LPS to assess the DC maturation. CCL-34 induced DC maturation according to their characteristically dendrite-forming morphology, CD83 expression and IL-12p70 production. The allostimulatory activity of DC on proliferation of naive CD4+CD45+RA+ T cells and their secretion of interferon-γ was increased by CCL-34. Phagocytosis, an important function of immature DC, was reduced after CCL-34 treatment. All these effects related to DC maturation were evidently induced by positive control LPS but not by CCL-44 treatment. TLR4 neutralization impaired human DC maturation triggered by CCL-34. The induction of IL-12, a hallmark of DC maturation, by CCL-34 and LPS was only evident in TLR4-competent C3H/HeN, but not in TLR4-defective C3H/HeJ mice. CCL-34 could further elicit the antigen presentation capability in mice inoculated with doxorubicin-treated colorectal Cancer cells. In summary, CCL-34 triggers DC maturation via a TLR4-dependent manner, which supports its potential application as an immunostimulator.

Keywords

CCL-34; TLR4; dendritic cell; differentiation; maturation.

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