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Environmental cues regulate epigenetic reprogramming of airway-resident memory CD8+ T cells.
Hayward, Sarah L; Scharer, Christopher D; Cartwright, Emily K; Takamura, Shiki; Li, Zheng-Rong Tiger; Boss, Jeremy M; Kohlmeier, Jacob E.
Afiliação
  • Hayward SL; Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA, USA.
  • Scharer CD; Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA, USA.
  • Cartwright EK; Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA, USA.
  • Takamura S; Department of Immunology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
  • Li ZT; Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA, USA.
  • Boss JM; Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA, USA.
  • Kohlmeier JE; Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA, USA. jkohlmeier@emory.edu.
Nat Immunol ; 21(3): 309-320, 2020 03.
Article em En | MEDLINE | ID: mdl-31953534
ABSTRACT
Tissue-resident memory T cells (TRM cells) are critical for cellular immunity to respiratory pathogens and reside in both the airways and the interstitium. In the present study, we found that the airway environment drove transcriptional and epigenetic changes that specifically regulated the cytolytic functions of airway TRM cells and promoted apoptosis due to amino acid starvation and activation of the integrated stress response. Comparison of airway TRM cells and splenic effector-memory T cells transferred into the airways indicated that the environment was necessary to activate these pathways, but did not induce TRM cell lineage reprogramming. Importantly, activation of the integrated stress response was reversed in airway TRM cells placed in a nutrient-rich environment. Our data defined the genetic programs of distinct lung TRM cell populations and show that local environmental cues altered airway TRM cells to limit cytolytic function and promote cell death, which ultimately leads to fewer TRM cells in the lung.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfócitos T CD8-Positivos / Epigênese Genética / Reprogramação Celular / Memória Imunológica / Pulmão Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfócitos T CD8-Positivos / Epigênese Genética / Reprogramação Celular / Memória Imunológica / Pulmão Idioma: En Ano de publicação: 2020 Tipo de documento: Article