Human thymic stromal lymphopoietin preferentially stimulates myeloid cells

PA Reche, V Soumelis, DM Gorman… - The Journal of …, 2001 - journals.aai.org
PA Reche, V Soumelis, DM Gorman, T Clifford, M Liu, M Travis, SM Zurawski, J Johnston…
The Journal of Immunology, 2001journals.aai.org
The sequence of a novel hemopoietic cytokine was discovered in a computational screen of
genomic databases, and its homology to mouse thymic stromal lymphopoietin (TSLP)
suggests that it is the human orthologue. Human TSLP is proposed to signal through a
heterodimeric receptor complex that consists of a new member of the hemopoietin family
termed human TSLP receptor and the IL-7R α-chain. Cells transfected with both receptor
subunits proliferated in response to purified, recombinant human TSLP, with induced …
Abstract
The sequence of a novel hemopoietic cytokine was discovered in a computational screen of genomic databases, and its homology to mouse thymic stromal lymphopoietin (TSLP) suggests that it is the human orthologue. Human TSLP is proposed to signal through a heterodimeric receptor complex that consists of a new member of the hemopoietin family termed human TSLP receptor and the IL-7R α-chain. Cells transfected with both receptor subunits proliferated in response to purified, recombinant human TSLP, with induced phosphorylation of Stat3 and Stat5. Human TSLPR and IL-7Rα are principally coexpressed on monocytes and dendritic cell populations and to a much lesser extent on various lymphoid cells. In accord, we find that human TSLP functions mainly on myeloid cells; it induces the release of T cell-attracting chemokines from monocytes and, in particular, enhances the maturation of CD11c+ dendritic cells, as evidenced by the strong induction of the costimulatory molecules CD40 and CD80 and the enhanced capacity to elicit proliferation of naive T cells.
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