Interleukin-4 is chemotactic for mouse macrophages

  • Cell Immunol. 1992 Jan;139(1):72-80. doi: 10.1016/0008-8749(92)90100-4.
A A Hiester  1 D R Metcalf P A Campbell
Affiliations
  • 1. Department of Medicine, National Jewish Center for Immunology and Respiratory Medicine, Denver, Colorado 80206.
Abstract

An important component of the cell-mediated immune response often is the migration of Macrophages to the site of immune activity. Although much evidence suggests that macrophage migration is regulated by antigen-specific T cells, the influence of T cell-derived cytokines on macrophage chemotaxis has not been well studied. Here we present evidence that interleukin-4 (IL-4), a cytokine derived from T helper 2 (Th 2) cells, is chemotactic for mouse peritoneal Macrophages. In an in vitro chemotaxis assay using Boyden chambers, Recombinant IL-4 was chemotactic for mouse peritoneal exudate Macrophages. This response was inhibited in a dose-dependent manner by the anti-IL-4 antibody, 11B11. As shown here and previously, interleukin-2 (IL-2) and interferon-gamma (IFN-gamma), cytokines derived from T helper 1 cells, are not chemotactic for mouse Macrophages.

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