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<dc:title xml:lang="en">Transcriptome Profiling of Porcine Naïve, Intermediate and Terminally Differentiated CD8+ T Cells</dc:title>

  
<dc:description xml:lang="en">The pig has the potential to become a leading research model for human diseases, pharmacological and transplantation studies. Since there are many similarities between humans and pigs, especially concerning anatomy, physiology and metabolism, there is necessity for a better understanding of the porcine immune system. In adaptive immunity, cytotoxic T lymphocytes (CTLs) are essential for host defense. However, most data on CTLs come from studies in mice, non-human primates and humans, while detailed information about porcine CD8+ CTLs is still sparse. Aim of this study was to analyze transcriptomes of three subsets of porcine CD8β+ T-cell subsets by using next-generation sequencing technology. Specifically, we described transcriptional profiles of subsets defined by their CD11a/CD27 expression pattern, postulated as naïve (CD8β+CD27+CD11alow), intermediate differentiated (CD8β+CD27dimCD11a+), and terminally differentiated cells (CD8β+CD27-CD11ahigh). Cells were analyzed in ex vivo condition as well as upon in vitro stimulation with concanavalin A (ConA) and PMA/ionomycin. Our analyses show that the highest number of differentially expressed genes was identified between naïve and terminally differentiated CD8+ T-cell subsets, underlining their difference in gene expression signature and respective differentiation stages. Moreover, genes related to early (IL7-R, CCR7, SELL, TCF7, LEF1, BACH2, SATB1, ZEB1 and BCL2) and late (KLRG1, TBX21, PRDM1, CX3CR1, ZEB2, ZNF683, BATF, EZH2 and ID2) stages of CD8+ T-cell differentiation were highly expressed in the naïve and terminally differentiated CD8+ T-cell subsets, respectively. Intermediate differentiated CD8+ T-cell subsets shared a more comparable gene expression profile associated with later stages of T-cell differentiation. Genes associated with cytolytic activity (GNLY, PRF1, GZMB, FASL, IFNG and TNF) were highly expressed in terminally and intermediate differentiated CD8+ T-cell subsets, while naïve CD8+ T cells lacked expression even after in vitro stimulation. Overall, PMA/ionomycin stimulation induced much stronger upregulation of genes compared to stimulation with ConA. Taken together, we provided comprehensive results showing transcriptional profiles of three differentiation stages of porcine CD8+ T-cell subsets. In addition, our study provides a powerful toolbox for the identification of candidate markers to characterize porcine immune cell subsets in more detail.</dc:description>

  
<dc:identifier rdf:resource="https://phaidra.vetmeduni.ac.at/o:1806"></dc:identifier>

  
<dc:language>en</dc:language>

  
<edm:type>TEXT</edm:type>

  
<dc:type xml:lang="en">article</dc:type>

  
<dc:subject xml:lang="en">Cytotoxic-T; Effector; Memory; Expression; Receptor; Subsets; Virus; Lymphocytes; Infection; Responses</dc:subject>

  
<dcterms:issued>2022</dcterms:issued>

  
<dc:date>2022</dc:date>

  
<dc:creator>Lagumdzic, Emil (University of Veterinary Medicine Vienna)</dc:creator>

  
<dc:creator>Mair, Kerstin H. (University of Veterinary Medicine Vienna)</dc:creator>

  
<dc:creator>Saalmüller, Armin (University of Veterinary Medicine Vienna)</dc:creator>

  
<dc:creator>Schmitt, Michael W. (Merck Healthcare KGaA)</dc:creator>

  
<dc:creator>Olgiati, Simone (Istituto di Ricerche Biomediche &quot;A. Marxer&quot; RBM S.p.A.)</dc:creator>

  
<dc:creator>Pernold, Clara (University of Veterinary Medicine Vienna)</dc:creator>

  
<dc:creator>Viano, Marta (Istituto di Ricerche Biomediche &quot;A. Marxer&quot; RBM S.p.A.)</dc:creator>

  
<dc:publisher>Frontiers Media Sa</dc:publisher>

  
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