Innateness transcriptome gradients characterize mouse T lymphocyte populations

A fundamental dichotomy in lymphocytes separates adaptive T and B lymphocytes, with clonally expressed antigen receptors, from innate lymphocytes, which carry out more rapid responses. Some T cell populations, however, are intermediates between these 2 poles, with the capacity to respond rapidly through T cell receptor activation or by cytokine stimulation. Here, using publicly available datasets, we constructed linear mixed models that not only define a gradient of innate gene expression in common for mouse innate-like T cells, but also are applicable to other mouse T lymphoid populations. A similar gradient could be identified for chromatin landscape based on ATAC-seq (assay for transposase-accessible chromatin using sequencing) data. The gradient included increased transcripts related to many traits of innate immune responses, with increased scores related to evidence for antigen experience. While including genes typical for T helper 1 (Th1) responses, the innateness gene program could be separated from Th1, Th2, and Th17 responses. Lymphocyte populations with higher innateness scores correlated with lower calcium-dependent T cell receptor-mediated cell activation, with some downstream signaling proteins dependent on calcium or affecting metabolism prephosphorylation. Therefore, as a group, different mouse innate-like T cell populations had related gene expression programs and activation pathways that are different from naive CD4 and CD8 T cells.

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Publication Details

Journal
The Journal of Immunology
Published
2025-02-01
DOI
https://doi.org/10.1093/jimmun/vkae015
Citations
1
Primary Topic
IL-33, ST2, and ILC Pathways
Type
article
Field-Weighted Citation Impact
0.80

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article

Innateness transcriptome gradients characterize mouse T lymphocyte populations

Viankail Cedillo-Castelán, Mitchell Kronenberg, Shilpi Chandra, Hsin‐Yu Liu et al.
1 citations
The Journal of Immunology
IL-33, ST2, and ILC Pathways
0.80
article

Innateness transcriptome gradients characterize mouse T lymphocyte populations

Viankail Cedillo-Castelán, Mitchell Kronenberg, Shilpi Chandra, Hsin‐Yu Liu, Eleni Phung, M. Murray, Hilde Cheroutre, Greet Verstichel, Gabriel Ascui, Alba Mendis, C. Luna
article en
1 citations

Abstract

A fundamental dichotomy in lymphocytes separates adaptive T and B lymphocytes, with clonally expressed antigen receptors, from innate lymphocytes, which carry out more rapid responses. Some T cell populations, however, are intermediates between these 2 poles, with the capacity to respond rapidly through T cell receptor activation or by cytokine stimulation. Here, using publicly available datasets, we constructed linear mixed models that not only define a gradient of innate gene expression in common for mouse innate-like T cells, but also are applicable to other mouse T lymphoid populations. A similar gradient could be identified for chromatin landscape based on ATAC-seq (assay for transposase-accessible chromatin using sequencing) data. The gradient included increased transcripts related to many traits of innate immune responses, with increased scores related to evidence for antigen experience. While including genes typical for T helper 1 (Th1) responses, the innateness gene program could be separated from Th1, Th2, and Th17 responses. Lymphocyte populations with higher innateness scores correlated with lower calcium-dependent T cell receptor-mediated cell activation, with some downstream signaling proteins dependent on calcium or affecting metabolism prephosphorylation. Therefore, as a group, different mouse innate-like T cell populations had related gene expression programs and activation pathways that are different from naive CD4 and CD8 T cells.

The Journal of ImmunologyVol. 214(2)
La Jolla Institute for Immunology (US), University of California San Diego (US)
National Institutes of Health
Openalex Percentile: Top 31%
IL-33, ST2, and ILC Pathways
0.80
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