Cellular architecture shapes the naïve T cell response

Author:

Hale Benjamin D.1ORCID,Severin Yannik1ORCID,Graebnitz Fabienne2ORCID,Stark Dominique2ORCID,Guignard Daniel1ORCID,Mena Julien1ORCID,Festl Yasmin1,Lee Sohyon1ORCID,Hanimann Jacob1ORCID,Zangger Nathan S.2ORCID,Meier Michelle1ORCID,Goslings David3,Lamprecht Olga3ORCID,Frey Beat M.3ORCID,Oxenius Annette2ORCID,Snijder Berend145ORCID

Affiliation:

1. Institute of Molecular Systems Biology, Department of Biology, ETH Zürich, Zürich, Switzerland.

2. Institute of Microbiology, Department of Biology, ETH Zürich, Zürich, Switzerland.

3. Blood Transfusion Service Zürich, Swiss Red Cross (SRC), Schlieren, Switzerland.

4. Swiss Institute of Bioinformatics, Lausanne, Switzerland.

5. Comprehensive Cancer Center Zurich (CCCZ), Zürich, Switzerland.

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 (T Ø ) or absence (T O ) of nuclear envelope invaginations, changed with maturation, activation, and differentiation. Upon T cell receptor (TCR) stimulation, naïve T Ø cells displayed increased expression of the early-response gene Nr4a1 , dependent upon heightened calcium entry. Subsequently, in vitro differentiation revealed that T Ø cells generated effector-like cells more so compared with T O 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.

Publisher

American Association for the Advancement of Science (AAAS)

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