1. Academic Validation
  2. Macrophage-colony stimulating factor and interleukin-34 induce chemokines in human whole blood

Macrophage-colony stimulating factor and interleukin-34 induce chemokines in human whole blood

  • Cytokine. 2010 Dec;52(3):215-20. doi: 10.1016/j.cyto.2010.08.005.
Hiroyuki Eda 1 Jian Zhang Robert H Keith Marshall Michener David R Beidler Joseph B Monahan
Affiliations

Affiliation

  • 1 Discovery Biology, Global Research and Development, St. Louis Laboratories, Pfizer Inc., 700 Chesterfield Parkway West, Chesterfield, MO 63017, USA. [email protected]
Abstract

The aim of this study is to investigate if macrophage-colony stimulating factor (M-CSF) or interleukin-34 (IL-34) induces cytokines or chemokines using human whole blood (HWB) and if an M-CSF- or IL-34-induced cytokine or chemokine production from HWB is inhibited by soluble M-CSF receptor or c-Fms kinase inhibitors. Among eight cytokines or growth factors tested, only IL-6 level was increased by up to 6-fold by M-CSF or IL-34 in HWB. In contrast, chemokine levels (IP-10/CXCL10, IL-8/CXCL8, and MCP-1/CCL2) were dramatically increased by M-CSF or IL-34 in HWB while exhibiting a large variation among donors. Variability of the MCP-1 signal induced by M-CSF or IL-34 was relatively less among donors compared to the IP-10 and IL-8 signals. The elevation of these chemokine levels was significantly decreased by soluble M-CSF receptor, indicating the elevation of these chemokines was mediated by M-CSF or IL-34. Furthermore, GW2580, a c-Fms kinase inhibitor, inhibited the induction of MCP-1 by M-CSF or IL-34 in a concentration dependent manner. These indicate MCP-1 is the most appropriate chemokine target for a chemokine release assay to evaluate the potency of c-Fms kinase inhibitors and MCP-1 release assay using HWB would be useful, relevant tool for translational pharmacology of c-Fms kinase inhibitors.

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