IL-10 induces gene expression in macrophages: partial overlap with IL-5 but not with IL-4 induced genes

R Stumpo, M Kauer, S Martin, H Kolb - Cytokine, 2003 - Elsevier
R Stumpo, M Kauer, S Martin, H Kolb
Cytokine, 2003Elsevier
The hypothesis that IL-10, in addition to down-regulating pro-inflammatory activities of
macrophages, induces an alternative state of macrophage reactivity was tested. We
therefore conducted a systematic search for genes induced by IL-10 using the method of
suppression subtractive hybridisation. Of an initial 1300 candidate clones obtained, several
screening rounds led to the identification of 51 clones which were reproducibly at least
twofold up-regulated in mouse J774 macrophages in response to treatment with IL-10. Of …
The hypothesis that IL-10, in addition to down-regulating pro-inflammatory activities of macrophages, induces an alternative state of macrophage reactivity was tested. We therefore conducted a systematic search for genes induced by IL-10 using the method of suppression subtractive hybridisation. Of an initial 1300 candidate clones obtained, several screening rounds led to the identification of 51 clones which were reproducibly at least twofold up-regulated in mouse J774 macrophages in response to treatment with IL-10. Of these, 41 genes were homologous to known genes involved in cell metabolism or immunoregulation, five contained novel sequences and another five were homologous to ESTs without known function. One major finding was that about 25% of the IL-10 genes were also found expressed in response to IFNγ, and several of these also reappeared in IL-4 or IL-5 induced mRNA species. Hence, Th1 and Th2 type cytokines may elicit a common basal activation response in macrophages. The second major finding was that 57% of IL-10 induced genes reappeared in IL-5 induced mRNA but no more than 18% were also found in IL-4 induced mRNA of J774 cells. We conclude that the gene expression response to IL-10 in macrophages is partially different from the response to IL-5 and is substantially different from the response to IL-4, which suggests an unexpected diversity of biological phenotypes induced by different Th2 type cytokines.
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