Porcine γδ T lymphocytes can be categorized into two functionally and developmentally distinct subsets according to expression of CD2 and level of TCR
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
23359501
DOI
10.4049/jimmunol.1202890
PII: jimmunol.1202890
Knihovny.cz E-resources
- MeSH
- Antigens, CD1 genetics immunology MeSH
- CD2 Antigens genetics immunology MeSH
- CD8 Antigens genetics immunology MeSH
- Cell Differentiation immunology MeSH
- Cell Lineage immunology MeSH
- Gene Expression MeSH
- Interleukin-2 immunology MeSH
- Humans MeSH
- Mice MeSH
- Swine MeSH
- Cell Proliferation MeSH
- Receptors, Antigen, T-Cell, gamma-delta genetics immunology MeSH
- T-Lymphocyte Subsets cytology immunology MeSH
- T-Lymphocytes cytology immunology MeSH
- Thymocytes cytology immunology MeSH
- Thymus Gland cytology immunology MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Antigens, CD1 MeSH
- CD2 Antigens MeSH
- CD8 Antigens MeSH
- Interleukin-2 MeSH
- Receptors, Antigen, T-Cell, gamma-delta MeSH
Porcine γδ T cells have two levels of TCRγδ expression. Whereas TCRγδ(med) cells are mostly CD2(+)CD8(-) and CD2(+)CD8(+), TCRγδ(hi) cells are highly enriched for CD2(-)CD8(-). This distribution is independent of bacterial colonization and it is already established in the thymus prior to export of γδ cells to the periphery. Sorting and cultivation experiments revealed that CD2(-)CD8(-) γδ cells are unable to acquire CD2 and CD8, whereas CD2(+) subsets can gain or loose CD8. There is also differential susceptibility for proliferation between CD2(+) and CD2(-) γδ cells. Although CD2(-)CD8(-) almost do not proliferate, proliferation of CD2(+)CD8(-) and CD2(+)CD8(+) is substantial. Population of CD2(-) γδ cells is also absent in CD1(+) immature thymocytes. Additionally, subpopulations of CD2(+) and CD2(-) γδ cells in the thymus differ in expression of auxiliary surface molecules such as CD25, CD45RA/RC, and MHC class II. Moreover, TCRγδ(hi) cells can generate TCRγδ(med) cells but never the opposite. The only exception is the thymus, where a few TCRγδ(med) cells can be induced to TCRγδ(hi) but only under IL-2 influence. The repertoire of TCRδ is polyclonal in all subsets, indicating that there is the same extent of diversification and equal capability of immune responses. Results collectively indicate that CD2 expression determines two lineages of γδ cells that differ in many aspects. Because CD2(-) γδ cells are missing in the blood of humans and mice but are obvious in other members of γδ-high species such as ruminants and birds, our findings support the idea that circulating CD2(-) γδ T cells are a specific lineage.
References provided by Crossref.org
Guidelines for the use of flow cytometry and cell sorting in immunological studies (second edition)