STAT3-dependent IL-21 production from T helper cells regulates hematopoietic progenitor cell homeostasis

被引:31
作者
Kaplan, Mark H. [1 ,2 ]
Glosson, Nicole L. [1 ]
Stritesky, Gretta L. [1 ]
Yeh, Norman [1 ]
Kinzfogl, John [1 ]
Rohrabaugh, Sara L. [1 ]
Goswami, Ritobrata [1 ]
Duy Pham [1 ]
Levy, David E. [3 ]
Brutkiewicz, Randy R. [1 ]
Blum, Janice S. [1 ]
Cooper, Scott [1 ]
Hangoc, Giao [1 ]
Broxmeyer, Hal E. [1 ]
机构
[1] Indiana Univ Sch Med, Dept Microbiol & Immunol, Herman B Wells Ctr Pediat Res, Indianapolis, IN 46202 USA
[2] Indiana Univ Sch Med, Dept Pediat, Herman B Wells Ctr Pediat Res, Indianapolis, IN 46202 USA
[3] NYU, Sch Med, Dept Pathol & Microbiol, New York, NY USA
关键词
TH1; CELLS; STAT3; INTERLEUKIN-21; GENERATION; MICE; DIFFERENTIATION; RESPONSES; CYTOKINE;
D O I
10.1182/blood-2011-02-334367
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The contribution of specific cell types to the production of cytokines that regulate hematopoiesis is still not well defined. We have previously identified T cell-dependent regulation of hematopoietic progenitor cell (HPC) numbers and cycling. In this report, we demonstrated that HPC activity is decreased in mice with STAT3-deficient T cells, a phenotype that is not because of decreased expression of IL-17 or ROR gamma t. STAT3 expression in T cells was required for IL-21 production by multiple T helper subsets, and neutralization of IL-21 resulted in decreased HPC activity identical to that in mice with STAT3-deficient T cells. Importantly, injection of IL-21 rescued HPC activity in mice with STAT3-deficient T cells. Thus, STAT3-dependent IL-21 production in T cells is required for HPC homeostasis. (Blood. 2011;117(23):6198-6201)
引用
收藏
页码:6198 / 6201
页数:4
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