4.5 Article

Collagen I enhances functional activities of human monocyte-derived dendritic cells via discoidin domain receptor 2

Journal

CELLULAR IMMUNOLOGY
Volume 278, Issue 1-2, Pages 95-102

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.cellimm.2012.07.004

Keywords

Human monocyte-derived dendritic cells; Collagen; Discoidin domain receptors; Interleukin-12; Maturation; Melanoma

Funding

  1. National Research Foundation of Korea (NRF)
  2. Ministry of Education, Science and Technology [2011-0013855]
  3. National Research Foundation of Korea [2011-0013855] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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We evaluated the involvement of collagen and their discoidin domain receptors (DDRs), DDR1 and DDR2, on the activation of human monocyte-derived dendritic cells (hDCs). DDR2 was markedly expressed on mature hDCs in comparison to immature ones. Collagen I enhanced the release of IL-12p40, TNF-alpha and IFN-gamma by hDCs. Additionally, hDCs exhibited enhanced expression of costimulatory molecules, and potent functional activities which, in turn, has therapeutic value. Interestingly, DDR2 depletion showed decrease in capacity of hDCs to stimulate T cells proliferation, whereas DDR1 silencing had no significant affect. These data demonstrate that DDR2 enhances hDCs activation and contributes to their functional activities. In addition, application of collagen I treated dendritic cells (DCs) vaccine reduced tumor burden giving longer survival in melanoma mice. Our study suggests that collagen I may enhance functional activities of DCs in immune response. (C) 2012 Elsevier Inc. All rights reserved.

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