Figure 5.
Figure 5. Sensitization of cord blood Tregs toward CD95L-mediated cell death in response to TCR stimulation. FACS-sorted cord blood Tregs (CD4+CD25+) and adult Tregs (CD4+CD25hi) were incubated with anti-CD3/CD28 mAbs and IL-2 as described in “Materials and methods.” CD95 expression (A-B, •) and CD45RO expression (B, ○) were determined at the time points indicated. (C) Six days after TCR stimulation, cord blood Tregs were incubated with CD95L (1:20) for 10 hours, and specific cell death rate was determined and compared with the specific cell death rate of freshly isolated cord blood Tregs. Likewise, freshly isolated FACS-sorted CD45ROlo cord blood Tregs without CD95hi memory Tregs (Figure 3B) were incubated with CD95L (1:20) for 10 hours. (D) Proliferation assays were used to measure the inhibitory capacities of freshly isolated cord blood Tregs or 6-day activated Tregs (anti-CD3/CD28 mAbs plus IL-2). For this test, Tconvs were FACS sorted from an adult donor and incubated with cord blood Tregs as described in “Materials and methods.” (E-F) Apoptosis-resistant Tregs were incubated with anti-CD3/CD28 mAbs plus IL-2 as described in “Materials and methods.” After 6 days, CD95 sensitivity toward CD95-mediated apoptosis (E) and expression of CD95 (F) were determined. One representative experiment of at least 3 independent experiments is shown. Error bars represent SEM.

Sensitization of cord blood Tregs toward CD95L-mediated cell death in response to TCR stimulation. FACS-sorted cord blood Tregs (CD4+CD25+) and adult Tregs (CD4+CD25hi) were incubated with anti-CD3/CD28 mAbs and IL-2 as described in “Materials and methods.” CD95 expression (A-B, •) and CD45RO expression (B, ○) were determined at the time points indicated. (C) Six days after TCR stimulation, cord blood Tregs were incubated with CD95L (1:20) for 10 hours, and specific cell death rate was determined and compared with the specific cell death rate of freshly isolated cord blood Tregs. Likewise, freshly isolated FACS-sorted CD45ROlo cord blood Tregs without CD95hi memory Tregs (Figure 3B) were incubated with CD95L (1:20) for 10 hours. (D) Proliferation assays were used to measure the inhibitory capacities of freshly isolated cord blood Tregs or 6-day activated Tregs (anti-CD3/CD28 mAbs plus IL-2). For this test, Tconvs were FACS sorted from an adult donor and incubated with cord blood Tregs as described in “Materials and methods.” (E-F) Apoptosis-resistant Tregs were incubated with anti-CD3/CD28 mAbs plus IL-2 as described in “Materials and methods.” After 6 days, CD95 sensitivity toward CD95-mediated apoptosis (E) and expression of CD95 (F) were determined. One representative experiment of at least 3 independent experiments is shown. Error bars represent SEM.

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