Cellular architecture shapes the naïve T cell response.
basic_science · Level V
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- Record sourced from PubMed, PMID 38843327.
- Also identified by DOI 10.1126/science.adh8967.
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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<sub>Ø</sub>) or absence (T<sub>O</sub>) of nuclear envelope invaginations, changed with maturation, activation, and differentiation. Upon T cell receptor (TCR) stimulation, naïve T<sub>Ø</sub> cells displayed increased expression of the early-response gene <i>Nr4a1</i>, dependent upon heightened calcium entry. Subsequently, in vitro differentiation revealed that T<sub>Ø</sub> cells generated effector-like cells more so compared with T<sub>O</sub> 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.
Medical subject headings
- CD8-Positive T-Lymphocytes
- Nuclear Receptor Subfamily 4, Group A, Member 1
- Receptors, Antigen, T-Cell