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Requirement of Endogenous Stem Cell Factor and Granulocyte-Colony-Stimulating Factor for IL-17-Mediated Granulopoiesis
Author(s) -
Paul Schwarzenberger,
Weitao Huang,
Ye Peng,
Peter Oliver,
Misty Manuel,
Zili Zhang,
Gregory Bagby,
Steve Nelson,
Jay K. Kolls
Publication year - 2000
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.164.9.4783
Subject(s) - granulopoiesis , neutrophilia , haematopoiesis , granulocyte colony stimulating factor , myelopoiesis , stem cell factor , granulocyte , immunology , myeloid , progenitor cell , biology , stem cell , cytokine , interleukin 3 , microbiology and biotechnology , t cell , immune system , interleukin 21 , genetics , chemotherapy
IL-17 is a novel, CD4+ T cell-restricted cytokine. In vivo, it stimulates hematopoiesis and causes neutrophilia consisting of mature granulocytes. In this study, we show that IL-17-mediated granulopoiesis requires G-CSF release and the presence or induction of the transmembrane form of stem cell factor (SCF) for optimal granulopoiesis. However, IL-17 also protects mice from G-CSF neutralization-induced neutropenia. G-CSF neutralization completely reversed IL-17-induced BM progenitor expansion, whereas splenic CFU-GM/CFU-granulocyte-erythrocyte-megakaryocyte-monocyte was only reduced by 50% in both Sl/Sld and littermate control mice. Thus, there remained a significant SCF/G-CSF-independent effect of IL-17 on splenic granulopoiesis, resulting in a preservation of mature circulating granulocytes. IL-17 is a cytokine that potentially interconnects lymphocytic and myeloid host defense and may have potential for therapeutic development.

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