T cell interleukin-17 induces stromal cells to produce proinflammatory and hematopoietic cytokines
Autor: | Smina Ait-Yahia, François Fossiez, Claude Gaillard, Eric Garcia, C Maat, B Das Mahapatra, Jean-Jacques Pin, Leopoldo Flores-Romo, E Rouvier, Pierre Golstein, Sem Saeland, Pierre Garrone, Odile Djossou, D Blanchard, Jacques Banchereau, Serge Lebecque, Pascale Chomarat |
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Rok vydání: | 1996 |
Předmět: |
T-Lymphocytes
Arthritis Rheumatoid Mice Reference Values Granulocyte Colony-Stimulating Factor Immunology and Allergy Cytotoxic T cell Lymphocytes Skin Interleukin-17 Synovial Membrane Interleukin Articles Recombinant Proteins Cell biology medicine.anatomical_structure Cytokines Interleukin 17 endocrine system Macromolecular Substances T cell Molecular Sequence Data Immunology Biology Transfection Dinoprostone Herpesvirus 2 Saimiriine Proinflammatory cytokine Interferon-gamma Open Reading Frames Viral Proteins Immune system Antigen medicine Animals Humans Amino Acid Sequence Interleukin 8 Inflammation Base Sequence Sequence Homology Amino Acid Interleukin-6 Tumor Necrosis Factor-alpha Interleukins Interleukin-8 Fibroblasts Hematopoietic Stem Cells Hematopoiesis Endothelium Vascular Stromal Cells |
Zdroj: | The Journal of Experimental Medicine |
ISSN: | 1540-9538 0022-1007 |
DOI: | 10.1084/jem.183.6.2593 |
Popis: | Analysis of the cDNA encoding murine interleukin (IL) 17 (cytotoxic T lymphocyte associated antigen 8) predicted a secreted protein sharing 57% amino acid identity with the protein predicted from ORF13, an open reading frame of Herpesvirus saimiri. Here we report on the cloning of human IL-17 (hIL-17), the human counterpart of murine IL-17. hIL-17 is a glycoprotein of 155 amino acids secreted as an homodimer by activated memory CD4+ T cells. Although devoid of direct effects on cells of hematopoietic origin, hIL-17 and the product of its viral counterpart, ORF13, stimulate epithelial, endothelial, and fibroblastic cells to secrete cytokines such as IL-6, IL-8, and granulocyte-colony-stimulating factor, as well as prostaglandin E2. Furthermore, when cultured in the presence of hIL-17, fibroblasts could sustain the proliferation of CD34+ hematopoietic progenitors and their preferential maturation into neutrophils. These observations suggest that hIL-17 may constitute (a) an early initiator of the T cell-dependent inflammmatory reaction; and (b) an element of the cytokine network that bridges the immune system to hematopoiesis. |
Databáze: | OpenAIRE |
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