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Cellular architecture shapes the naïve T cell response.
Hale, Benjamin D; Severin, Yannik; Graebnitz, Fabienne; Stark, Dominique; Guignard, Daniel; Mena, Julien; Festl, Yasmin; Lee, Sohyon; Hanimann, Jacob; Zangger, Nathan S; Meier, Michelle; Goslings, David; Lamprecht, Olga; Frey, Beat M; Oxenius, Annette; Snijder, Berend.
Affiliation
  • Hale BD; Institute of Molecular Systems Biology, Department of Biology, ETH Zürich, Zürich, Switzerland.
  • Severin Y; Institute of Molecular Systems Biology, Department of Biology, ETH Zürich, Zürich, Switzerland.
  • Graebnitz F; Institute of Microbiology, Department of Biology, ETH Zürich, Zürich, Switzerland.
  • Stark D; Institute of Microbiology, Department of Biology, ETH Zürich, Zürich, Switzerland.
  • Guignard D; Institute of Molecular Systems Biology, Department of Biology, ETH Zürich, Zürich, Switzerland.
  • Mena J; Institute of Molecular Systems Biology, Department of Biology, ETH Zürich, Zürich, Switzerland.
  • Festl Y; Institute of Molecular Systems Biology, Department of Biology, ETH Zürich, Zürich, Switzerland.
  • Lee S; Institute of Molecular Systems Biology, Department of Biology, ETH Zürich, Zürich, Switzerland.
  • Hanimann J; Institute of Molecular Systems Biology, Department of Biology, ETH Zürich, Zürich, Switzerland.
  • Zangger NS; Institute of Microbiology, Department of Biology, ETH Zürich, Zürich, Switzerland.
  • Meier M; Institute of Molecular Systems Biology, Department of Biology, ETH Zürich, Zürich, Switzerland.
  • Goslings D; Blood Transfusion Service Zürich, Swiss Red Cross (SRC), Schlieren, Switzerland.
  • Lamprecht O; Blood Transfusion Service Zürich, Swiss Red Cross (SRC), Schlieren, Switzerland.
  • Frey BM; Blood Transfusion Service Zürich, Swiss Red Cross (SRC), Schlieren, Switzerland.
  • Oxenius A; Institute of Microbiology, Department of Biology, ETH Zürich, Zürich, Switzerland.
  • Snijder B; Institute of Molecular Systems Biology, Department of Biology, ETH Zürich, Zürich, Switzerland.
Science ; 384(6700): eadh8697, 2024 Jun 07.
Article de En | MEDLINE | ID: mdl-38843327
ABSTRACT
After antigen stimulation, naïve T cells display reproducible population-level responses, which arise from individual T cells pursuing specific differentiation trajectories. However, cell-intrinsic predeterminants controlling these single-cell decisions remain enigmatic. We found that the subcellular architectures of naïve CD8 T cells, defined by the presence (TØ) or absence (TO) of nuclear envelope invaginations, changed with maturation, activation, and differentiation. Upon T cell receptor (TCR) stimulation, naïve TØ cells displayed increased expression of the early-response gene Nr4a1, dependent upon heightened calcium entry. Subsequently, in vitro differentiation revealed that TØ cells generated effector-like cells more so compared with TO cells, which proliferated less and preferentially adopted a memory-precursor phenotype. These data suggest that cellular architecture may be a predeterminant of naïve CD8 T cell fate.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Récepteurs aux antigènes des cellules T / Lymphocytes T CD8/ / Membre-1 du groupe A de la sous-famille-4 de récepteurs nucléaires Limites: Animals / Humans Langue: En Journal: Science Année: 2024 Type de document: Article Pays d'affiliation: Suisse Pays de publication: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Récepteurs aux antigènes des cellules T / Lymphocytes T CD8/ / Membre-1 du groupe A de la sous-famille-4 de récepteurs nucléaires Limites: Animals / Humans Langue: En Journal: Science Année: 2024 Type de document: Article Pays d'affiliation: Suisse Pays de publication: États-Unis d'Amérique