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Paracrine IL-2 Is Required for Optimal Type 2 Effector Cytokine Production.
Olson, Matthew R; Ulrich, Benjamin J; Hummel, Sarah A; Khan, Ibrahim; Meuris, Brice; Cherukuri, Yesesri; Dent, Alexander L; Janga, Sarath Chandra; Kaplan, Mark H.
Afiliação
  • Olson MR; Department of Pediatrics, Herman B Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN 46202; olsonmr@iupui.edu mkaplan2@iupui.edu.
  • Ulrich BJ; Department of Pediatrics, Herman B Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN 46202.
  • Hummel SA; Department of Pediatrics, Herman B Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN 46202.
  • Khan I; Department of Pediatrics, Herman B Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN 46202.
  • Meuris B; Department of Pediatrics, Herman B Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN 46202.
  • Cherukuri Y; School of Informatics and Computing, Indiana University-Purdue University Indianapolis, Indianapolis, IN 46202; and.
  • Dent AL; Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, IN 46202.
  • Janga SC; School of Informatics and Computing, Indiana University-Purdue University Indianapolis, Indianapolis, IN 46202; and.
  • Kaplan MH; Department of Pediatrics, Herman B Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN 46202; olsonmr@iupui.edu mkaplan2@iupui.edu.
J Immunol ; 198(11): 4352-4359, 2017 06 01.
Article em En | MEDLINE | ID: mdl-28468971
ABSTRACT
IL-2 is a pleiotropic cytokine that promotes the differentiation of Th cell subsets, including Th1, Th2, and Th9 cells, but it impairs the development of Th17 and T follicular helper cells. Although IL-2 is produced by all polarized Th subsets to some level, how it impacts cytokine production when effector T cells are restimulated is unknown. We show in this article that Golgi transport inhibitors (GTIs) blocked IL-9 production. Mechanistically, GTIs blocked secretion of IL-2 that normally feeds back in a paracrine manner to promote STAT5 activation and IL-9 production. IL-2 feedback had no effect on Th1- or Th17-signature cytokine production, but it promoted Th2- and Th9-associated cytokine expression. These data suggest that the use of GTIs results in an underestimation of the presence of type 2 cytokine-secreting cells and highlight IL-2 as a critical component in optimal cytokine production by Th2 and Th9 cells in vitro and in vivo.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Citocinas / Interleucina-2 / Interleucina-9 / Células Th2 / Comunicação Parácrina Limite: Animals Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Citocinas / Interleucina-2 / Interleucina-9 / Células Th2 / Comunicação Parácrina Limite: Animals Idioma: En Ano de publicação: 2017 Tipo de documento: Article