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Science ; 384(6700): eadh8697, 2024 Jun 07.
Article in English | 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.


Subject(s)
CD8-Positive T-Lymphocytes , Nuclear Receptor Subfamily 4, Group A, Member 1 , Receptors, Antigen, T-Cell , Animals , Mice , Calcium/metabolism , CD8-Positive T-Lymphocytes/immunology , CD8-Positive T-Lymphocytes/ultrastructure , Cell Differentiation , Immunologic Memory , Lymphocyte Activation , Mice, Inbred C57BL , Nuclear Envelope/metabolism , Nuclear Receptor Subfamily 4, Group A, Member 1/genetics , Nuclear Receptor Subfamily 4, Group A, Member 1/metabolism , Receptors, Antigen, T-Cell/immunology , Receptors, Antigen, T-Cell/metabolism , Microscopy, Fluorescence , Fluorescent Antibody Technique , Humans
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