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April 1, 1991The Journal of Experimental Medicine188 citationsOpen Access

Interleukin 7 induces cytokine secretion and tumoricidal activity by human peripheral blood monocytes.

MAMark R. AldersonTTTeresa W. ToughSZSteven F. Ziegler

Key Points

  • The research aims to explore how interleukin 7 affects cytokine secretion and tumoricidal activity in human peripheral blood monocytes.
  • Analyzed cytokine secretion in response to IL-7, IL-1 beta, and LPS in peripheral blood mononuclear cells.
  • Used cytokine assays (B9 hybridoma growth factor assay, enzyme-linked immunosorbent assay) and Northern hybridization for analysis.
  • Investigated the effects of IL-4 on IL-6 secretion from monocytes.
  • IL-7 induced IL-6 secretion from monocytes that was 10-fold more than IL-1 beta at optimal concentrations.
  • IL-7 also stimulated secretion of TNF-alpha, IL-1 alpha, and IL-1 beta by monocytes.
  • IL-7 prompted tumoricidal activity against melanoma cells, linking cytokine output to potential anti-tumor effects.

Abstract

Peripheral blood monocytes can be induced by stimuli such as bacterial lipopolysaccharide (LPS) to secrete an array of cytokines. We have studied the effects of interleukin 7 (IL-7) on human peripheral blood mononuclear cells (PBMC) and found that IL-7 is a relatively potent inducer of IL-6 secretion IL-6 protein levels were determined either by the B9 hybridoma growth factor assay or by enzyme-linked immunosorbent assay, and mRNA for IL-6 was analyzed by Northern hybridization. Detailed examination revealed that, among PBMC, monocytes, rather than lymphocytes, were secreting IL-6 in response to IL-7. In contrast to the low concentrations of IL-7 required to stimulate T cell growth and differentiation (as low as 0.1 ng/ml), relatively high concentrations of IL-7 were necessary to induce IL-6 secretion by monocytes (at least 10 ng/ml). An optimal concentration of IL-7 (100 ng/ml) induced monocytes to secrete 10-fold more IL-6 than an optimal concentration of IL-1 beta (10 ng/ml), and almost as much as LPS. However, significantly more IL-7 than IL-1 beta was required to induce detectable levels of IL-6. The kinetics of IL-6 secretion by monocytes were identical in response to IL-7, IL-1 beta, or LPS, with IL-6 protein detectable in culture supernatants as early as 2 h after the initiation of culture. IL-4 was found to markedly inhibit the ability of IL-7 or LPS to induce IL-6 mRNA and IL-6 secretion. In addition to promoting IL-6 production, IL-7 induced the secretion of immunoreactive IL-1 alpha, IL-1 beta, and tumor necrosis factor alpha (TNF-alpha) by monocytes. IL-7 also induced monocyte/macrophage tumoricidal activity against a human melanoma cell target, an activity that may be related to the secretion of IL-1 alpha, IL-1 beta, and TNF-alpha. Finally, we used a whole blood culture system as a bridge to in vivo analysis to demonstrate that IL-7 induces cytokine secretion in the absence of culture medium, fetal calf serum, and adherence to plastic. Our data suggest that IL-7, in addition to regulating lymphocyte growth and differentiation, has potent effects on cells of the monocytic lineage. Thus, IL-7 may be an important mediator in inflammation and in the macrophage immune response to tumors.

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Cite This Study

Alderson et al. (1991) studied this question.

synapsesocial.com/papers/6a0e1dd82a2e27e73427a807https://doi.org/10.1084/jem.173.4.923
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