Characterization of transcription factor phenotypes within antigen-specific CD4+ T cells using qualitative multiplex single-cell RT-PCR

Current research on antigen specific CD4+ T cells indicates that there is functional and phenotypic heterogeneity within these populations, but the extent of this heterogeneity is poorly described. The CD134/CD25 assay allows live isolation of antigen specific cells in vitro for down-stream molecula...

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Veröffentlicht in:PloS one 2013-10, Vol.8 (10), p.e74946-e74946
Hauptverfasser: Phetsouphanh, Chansavath, Xu, Yin, Amin, Janaki, Seddiki, Nabila, Procopio, Francesco, Sekaly, Rafick Pierre, Zaunders, John J, Kelleher, Anthony D
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Sprache:eng
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Zusammenfassung:Current research on antigen specific CD4+ T cells indicates that there is functional and phenotypic heterogeneity within these populations, but the extent of this heterogeneity is poorly described. The CD134/CD25 assay allows live isolation of antigen specific cells in vitro for down-stream molecular analysis. Antigen specific CD4+ T cells were examined at the molecular level by lineage specific transcription factor profiling using qualitative multiplex single cell RT-PCR and Lock Nucleic Acid (LNA) probes allowed unbiased amplification and delineation of expression of Tbx21, Gata3, Rorc, Foxp3 and Bcl-6. It overcomes the limitations of previous assays by allowing identification of transcription factor mRNA in single antigen specific cells with high sensitivity (down to 10 femtograms) and specificity. Patterns of responses can be robustly characterized using
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0074946