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Sonic Hedgehog Regulates Early Human Thymocyte Differentiation by Counteracting the IL-7-Induced Development of CD34⁺ Precursor Cells¹

Cruz Gutiérrez-Frías^2,*, Rosa Sacedón^2,, Carmen Hernández-López^*, Teresa Cejalvo, Tessa Crompton, Agustín G. Zapata^*, Alberto Varas and Angeles Vicente^3,

^* Department of Cell Biology, Faculty of Biology, and Department of Cell Biology, Faculty of Medicine, Complutense University, Madrid, Spain; and Department of Biological Sciences, Imperial College London, London, United Kingdom

The Hedgehog (Hh) family of signaling molecules normally functions in the development of numerous tissues by regulating cellular differentiation and proliferation. Recent results have demonstrated that the different components of the Hh signaling pathway are expressed in the human thymus. In this study, we investigate the potential role of Sonic hedgehog (Shh) in human intrathymic T cell maturation. Results show that the expression of the two components of the Hh receptor, Patched and Smoothened, is mostly restricted to CD34⁺ precursor cells that are committing to the T cell lineage. Shh significantly increased the viability of CD34⁺ T cell precursors modulating bcl-2 and bax protein expression, and also inhibited their proliferation. The treatment of chimeric human-mouse fetal thymus organ cultures with Shh resulted in an arrested thymocyte differentiation and an accumulation of CD34⁺ progenitor cells. This effect was mainly attributed to the ability of Shh to counteract the IL-7-induced proliferation and differentiation of CD34⁺ cells. Shh down-regulated in the precursor cell population the expression of IL-7R as well as stromal-derived factor-1 chemokine receptor, CXCR4, and inhibited IL-7-dependent STAT5 phosphorylation. Therefore, Shh may function as a maintenance factor for intrathymic CD34⁺ precursor cells.

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