β-Chemokine production in CD40L-stimulated monocyte-derived macrophages requires activation of MAPK signaling pathways Article

Di Marzio, P, Sherry, B, Thomas, EK et al. (2003). β-Chemokine production in CD40L-stimulated monocyte-derived macrophages requires activation of MAPK signaling pathways . CYTOKINE, 23(3), 53-63. 10.1016/S1043-4666(03)00186-8

cited authors

  • Di Marzio, P; Sherry, B; Thomas, EK; Franchin, G; Schmidtmayerova, H; Bukrinsky, M

abstract

  • CD40 ligand is a cell surface molecule on CD4+ T cells that interacts with its receptor, CD40, on antigen presenting cells to mediate humoral and cellular immune responses. Our previous studies demonstrated that a trimeric soluble form of CD40L (CD40LT) activates macrophages to produce β-chemokines and decrease CCR5 and CD4 cell surface expression, thus inducing resistance to HIV-1 infection. However, the mechanism(s) by which CD40LT mediates these effects in primary macrophages remains unclear. In this report, we demonstrate that CD40LT induces synthesis of β-chemokines through the activation of MAPK signaling pathways. Treatment of macrophages with CD40LT results in a rapid activation of p38 and ERK1/2 mitogen-activated protein kinases. Inhibitors of these MAPKs blocked β-chemokine production, while protein kinase A and C inhibitors had little or no effect. We also provide evidence that CD40LT stimulates β-chemokine production directly, as well as indirectly via a TNF-α-dependent mechanism. At the early time points, CD40LT directly stimulated β-chemokine production, whereas at later time points the effect was mediated to some extent by TNF-α. In conclusion, our results suggest that CD40-CD40L interactions are important for the activation of monocyte-derived macrophage antiviral response affecting both viral replication and the recruitment of immune cells. © 2003 Elsevier Ltd. All rights reserved.

publication date

  • August 7, 2003

published in

Digital Object Identifier (DOI)

start page

  • 53

end page

  • 63

volume

  • 23

issue

  • 3