GLI2 regulates TGF-β1 in human CD4+ T cells: Implications in cancer and HIV pathogenesis

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Abstract

Elevated levels of the immunoregulatory cytokine TGF-β1 in cancer and HIV infection have been linked to the suppression of protective immune responses. The transcriptional regulation of TGF-β1 is complex and still not completely understood. We report here for the first time that the transcription factor GLI2 regulates the expression of TGF-β1 in human CD4+ T cells. In silico screening revealed five novel putative GLI binding sites in the human TGF-β1 promoter. At least two of these sites within the human TGF-β1 promoter are regulated by the GLI2 activator as knockdown of GLI2 in regulatory CD4+CD25hi T cells, high producers of TGF-β1, significantly decreased TGF-β1 transcription. Additionally, naïve CD4+ T cells, low producers of TGF-β1, increased their basal level of TGF-β1 mRNA following lentiviral infection with GLI2. The transcriptional regulation of TGF-β1 by GLI2 is a new extension to Sonic Hedgehog (SHH) and TGF-β1 cross-regulation and may provide insight into the detrimental elevation of TGF-β1 leading to pathogenesis in cancer and HIV infection. © 2012 Furler, Uittenbogaart.

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Furler, R. L., & Uittenbogaart, C. H. (2012). GLI2 regulates TGF-β1 in human CD4+ T cells: Implications in cancer and HIV pathogenesis. PLoS ONE, 7(7). https://doi.org/10.1371/journal.pone.0040874

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