<resource xmlns:datacite="http://datacite.org/schema/kernel-4">
<creators>
<creator>
<creatorName>Lagumdzic, Emil (University of Veterinary Medicine Vienna)</creatorName>
<givenName>Emil</givenName>
<familyName>Lagumdzic</familyName>
</creator>
<creator>
<creatorName>Mair, Kerstin H. (University of Veterinary Medicine Vienna)</creatorName>
<givenName>Kerstin H.</givenName>
<familyName>Mair</familyName>
</creator>
<creator>
<creatorName>Saalmüller, Armin (University of Veterinary Medicine Vienna)</creatorName>
<givenName>Armin</givenName>
<familyName>Saalmüller</familyName>
</creator>
<creator>
<creatorName>Schmitt, Michael W. (Merck Healthcare KGaA)</creatorName>
<givenName>Michael W.</givenName>
<familyName>Schmitt</familyName>
</creator>
<creator>
<creatorName>Olgiati, Simone (Istituto di Ricerche Biomediche "A. Marxer" RBM S.p.A.)</creatorName>
<givenName>Simone</givenName>
<familyName>Olgiati</familyName>
</creator>
<creator>
<creatorName>Pernold, Clara (University of Veterinary Medicine Vienna)</creatorName>
<givenName>Clara</givenName>
<familyName>Pernold</familyName>
</creator>
<creator>
<creatorName>Viano, Marta (Istituto di Ricerche Biomediche "A. Marxer" RBM S.p.A.)</creatorName>
<givenName>Marta</givenName>
<familyName>Viano</familyName>
</creator>
</creators>
<titles>
<title>Transcriptome Profiling of Porcine Naïve, Intermediate and Terminally Differentiated CD8+ T Cells</title>
</titles>
<publisher>Frontiers Media Sa</publisher>
<publicationYear>2022</publicationYear>
<descriptions>
<description descriptionType="Other">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.</description>
</descriptions>
<resourceType resourceTypeGeneral="Text">PDFDocument</resourceType>
<language>en</language>
<dates>
<date dateType="Created">2023-07-07T07:41:54.910Z</date>
</dates>
<subjects>
<subject>Cytotoxic-T; Effector; Memory; Expression; Receptor; Subsets; Virus; Lymphocytes; Infection; Responses</subject>
</subjects>
<sizes>
<size>6679833 b</size>
</sizes>
<formats>
<format>application/pdf</format>
</formats>
<rightsList>
<rights rightsURI="http://creativecommons.org/licenses/by/4.0/">CC BY 4.0 International</rights>
</rightsList>
</resource>
