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

Author:

Kaplan Mark H.12,Glosson Nicole L.1,Stritesky Gretta L.1,Yeh Norman1,Kinzfogl John1,Rohrabaugh Sara L.1,Goswami Ritobrata1,Pham Duy1,Levy David E.3,Brutkiewicz Randy R.1,Blum Janice S.1,Cooper Scott1,Hangoc Giao1,Broxmeyer Hal E.1

Affiliation:

1. Departments of Microbiology and Immunology, and

2. Pediatrics, Herman B Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN, and

3. Department of Pathology and Microbiology, New York University School of Medicine, New York, NY

Abstract

Abstract 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 RORγt. 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.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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