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May 1, 1997Cell2,369 citationsOpen Access

The Transcription Factor GATA-3 Is Necessary and Sufficient for Th2 Cytokine Gene Expression in CD4 T Cells

WZWei-ping ZhengRFRichard A. Flavell

Key Points

  • This research aims to clarify the role of GATA-3 in the differentiation and cytokine expression of Th2 cells from naive T cell precursors.
  • Examined GATA-3 expression in Th2 and Th1 cells
  • Used antisense GATA-3 to inhibit cytokine gene expression in Th2 clones
  • Tested transgenic mice with elevated GATA-3 in CD4 T cells
  • GATA-3 was selectively expressed in Th2 cells and present in naive T cells
  • Antisense GATA-3 significantly reduced Th2 cytokine gene expression
  • Transgenic mice expressing high GATA-3 in CD4 T cells showed increased Th2 cytokine gene expression.

Abstract

CD4 T cells potentiate the inflammatory or humoral immune response through the action of Th1 and Th2 cells, respectively. The molecular basis of the differentiation of these cells from naive T cell precursors is, however, unclear. We found that GATA-3 was selectively expressed in Th2 cells. GATA-3 is expressed at a high level in naive, freshly activated T cells and Th2 lineage cells, but subsides to a minimal level in Th1 lineage cells as naive cells commit to their Th subset. Antisense GATA-3 inhibited the expression of all Th2 cytokine genes in the Th2 clone D10. GATA-3 directly activated an IL-4 promoter-luciferase reporter gene in M12 cells. In transgenic mice, elevated GATA-3 in CD4 T cells caused Th2 cytokine gene expression in developing Th1 cells. Thus, GATA-3 is necessary and sufficient for Th2 cytokine gene expression.

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Cite This Study

Zheng et al. (1997) studied this question.

synapsesocial.com/papers/6a4275bada61c7ab7247aba2https://doi.org/10.1016/s0092-8674(00)80240-8
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