Dynamic regulation of Gata1 expression during the maturation of conventional dendritic cells

Objectives

To identify the regulatory sequences driving Gata1 expression in conventional dendritic cells (cDC).

Materials and Methods

The number and expression levels of Gata1, Gata1-target genes and hypersensitive site (HS) 2 (the eosinophil-specific enhancer)−driven green fluorescent protein (GFP) reporter of cDCs from mice lacking HS1 (the erythroid/megakaryocytic-specific enhancer, Gata1^low mutation) and wild-type littermates, as well as the response to lipopolysaccharide of ex vivo−generated wild-type and Gata1^low DCs were investigated.

Results

cDC maturation was associated with bell-shaped changes in Gata1 expression that peaked in cDCs precursors from blood. The Gata1^low mutation did not affect Gata1 expression in cDC precursors and these cells expressed the HS2-driven reporter, indicating that Gata1 expression is HS2-driven in these cells. By contrast, the Gata1^low mutation reduced Gata1 expression in mature cDCs and these cells did not express GFP, indicating that mature cDCs express Gata1 driven by HS1. In blood, the number of cDC precursors expressing CD40/CD80 was reduced in Gata1^low mice, while CD40^pos/CD80^pos cDC precursors from wild-type mice expressed the HS2-GFP reporter, suggesting that Gata1 expression in these cells is both HS1- and HS2-driven. In addition, the antigen and accessory molecules presentation process induced by lipopolysaccharide in ex vivo−generated wild-type DC was associated with increased acetylated histone 4 occupancy of HS1, while ex vivo−generated Gata1^low cDCs failed to respond to lipopolysaccharide, suggesting that HS1 activation is required for cDC maturation.

Conclusion

These results identify a dynamic pattern of Gata1 regulation that switches from an HS1 to an HS2-dependent phase during the maturation of cDCs associated with the antigen-presentation process in the blood.