胸腺基质淋巴细胞生成素
CD80
生物
细胞生物学
趋化因子
细胞因子
CD11c公司
免疫学
CD40
免疫系统
细胞毒性T细胞
遗传学
体外
表型
基因
作者
Pedro A. Reche,Vassili Soumelis,Daniel M. Gorman,Teresa Clifford,Man-Ru Liu,Marilyn Travis,Sandra Zurawski,Jim Johnston,Yong-Jun Liu,Hergen Spits,René de Waal Malefyt,Robert A. Kastelein,J. Fernando Bazán
出处
期刊:Journal of Immunology
[American Association of Immunologists]
日期:2001-07-01
卷期号:167 (1): 336-343
被引量:404
标识
DOI:10.4049/jimmunol.167.1.336
摘要
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 alpha-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-7Ralpha 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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