Early precursors and molecular determinants of tissue-resident memory CD8+ T lymphocytes revealed by single-cell RNA sequencing.
Nadia S KurdZhaoren HeTiani L LouisJ Justin MilnerKyla D OmilusikWenhao JinMatthew S TsaiChristella E WidjajaJad N KanbarJocelyn G OlveraTiffani TyslLauren K QuezadaBrigid S BolandWendy Jia Men HuangCornelis MurreAnanda W GoldrathGene W YeoJohn T ChangPublished in: Science immunology (2020)
During an immune response to microbial infection, CD8+ T cells give rise to distinct classes of cellular progeny that coordinately mediate clearance of the pathogen and provide long-lasting protection against reinfection, including a subset of noncirculating tissue-resident memory (TRM) cells that mediate potent protection within nonlymphoid tissues. Here, we used single-cell RNA sequencing to examine the gene expression patterns of individual CD8+ T cells in the spleen and small intestine intraepithelial lymphocyte (siIEL) compartment throughout the course of their differentiation in response to viral infection. These analyses revealed previously unknown transcriptional heterogeneity within the siIEL CD8+ T cell population at several stages of differentiation, representing functionally distinct TRM cell subsets and a subset of TRM cell precursors within the tissue early in infection. Together, these findings may inform strategies to optimize CD8+ T cell responses to protect against microbial infection and cancer.
Keyphrases
- single cell
- rna seq
- gene expression
- high throughput
- immune response
- microbial community
- induced apoptosis
- dna methylation
- patient safety
- working memory
- peripheral blood
- high grade
- quality improvement
- papillary thyroid
- stem cells
- squamous cell carcinoma
- cell cycle arrest
- mesenchymal stem cells
- inflammatory response
- toll like receptor
- bone marrow
- signaling pathway
- cell death
- cell therapy
- oxidative stress
- endoplasmic reticulum stress
- squamous cell
- single molecule
- emergency medicine
- childhood cancer