Figure 3
Figure 3. Intermediate (GFPlo) cells from neonates also produce greater levels of cytokine compared with intermediate (GFPlo) cells from adults. (A) CD4+ LN cells from RAG2p-GFP+/− neonates and adults were sorted into RTEs (GFPhi), intermediate (GFPlo), and resident (GFP−) populations. These purified neonatal (B) and adult (C) cells were then activated with PBαCD3 and αCD28 for 48 hours, and supernatants were harvested for cytokine-specific ELISA. (D) The data from panels B and C were regraphed to show a comparison of neonatal and adult RTEs and intermediate cells. Graphs represent pooled data from 4 or 5 independent experiments and are shown as the mean ± SEM; n = 35 to 60 neonates and 6 adults per experiment.

Intermediate (GFPlo) cells from neonates also produce greater levels of cytokine compared with intermediate (GFPlo) cells from adults. (A) CD4+ LN cells from RAG2p-GFP+/− neonates and adults were sorted into RTEs (GFPhi), intermediate (GFPlo), and resident (GFP) populations. These purified neonatal (B) and adult (C) cells were then activated with PBαCD3 and αCD28 for 48 hours, and supernatants were harvested for cytokine-specific ELISA. (D) The data from panels B and C were regraphed to show a comparison of neonatal and adult RTEs and intermediate cells. Graphs represent pooled data from 4 or 5 independent experiments and are shown as the mean ± SEM; n = 35 to 60 neonates and 6 adults per experiment.

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