Figure 4.
Figure 4. Resistance of cord blood Tregs toward CD95L-mediated cell death. (A) FACS-sorted adult Tregs (CD4+CD25hi), cord blood Tregs (CD4+CD25+), and their respective Tconvs were incubated with CD95L (1:20) for 10 hours, and specific cell death rates were determined by FACS analysis as described previously.12 Similarly, CD4+CD25+CD45ROlo T cells (R2) as well as CD4+CD25+CD45ROhi T cells (R1) were FACS sorted as shown in panel B, and all cells were incubated with CD95L (1:20) for 10 hours. Error bars represent SEM. (B) Enrichment of naive or memory cord blood Tregs by FACS sorting. Cord blood lymphocytes were stained with fluorochrome-labeled mAbs against CD4, CD25 and CD45RO. Previous to FACS sorting, one aliquot from the sort sample was additionally stained with anti-CD95 mAb to detect CD4+CD25+CD95hi T cells. Because CD4+CD25+CD95hi T cells cosegregate with CD45ROhi T cells (arrow), the sorting gate was set on CD45ROhi cells to separate CD4+CD25+CD45ROhi CD95hi memory T cells in R1 from the naive cord blood Tregs in R2. See the penultimate paragraph of “Results” for further explanation. One representative experiment of at least 3 independent experiments is shown.

Resistance of cord blood Tregs toward CD95L-mediated cell death. (A) FACS-sorted adult Tregs (CD4+CD25hi), cord blood Tregs (CD4+CD25+), and their respective Tconvs were incubated with CD95L (1:20) for 10 hours, and specific cell death rates were determined by FACS analysis as described previously.12  Similarly, CD4+CD25+CD45ROlo T cells (R2) as well as CD4+CD25+CD45ROhi T cells (R1) were FACS sorted as shown in panel B, and all cells were incubated with CD95L (1:20) for 10 hours. Error bars represent SEM. (B) Enrichment of naive or memory cord blood Tregs by FACS sorting. Cord blood lymphocytes were stained with fluorochrome-labeled mAbs against CD4, CD25 and CD45RO. Previous to FACS sorting, one aliquot from the sort sample was additionally stained with anti-CD95 mAb to detect CD4+CD25+CD95hi T cells. Because CD4+CD25+CD95hi T cells cosegregate with CD45ROhi T cells (arrow), the sorting gate was set on CD45ROhi cells to separate CD4+CD25+CD45ROhi CD95hi memory T cells in R1 from the naive cord blood Tregs in R2. See the penultimate paragraph of “Results” for further explanation. One representative experiment of at least 3 independent experiments is shown.

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