Figure 3
From: Preferential uptake of antioxidant carbon nanoparticles by T lymphocytes for immunomodulation

PEG-HCCs internalization is improved in activated T cells but is not biased towards major T cell subsets.
(a) PEG-HCC internalization in naïve (CD3+CD62L+) and memory (CD3+CD62L−) rat splenic T cells, analyzed by FCM (n = 3 splenic preparations). (b) PEG-HCC internalization in helper (CD3+CD4+, left) and cytotoxic (CD3+CD8+, right) rat splenic T cells, analyzed by FCM (n = 3 splenic preparations). A separate group of rat splenocytes cells were also stimulated with the mitogen, concanavalin A (1 μg/mL). (c) PEG-HCC internalization in the δγ T cell subset (CD3+δγ+) as compared to non-δγ T cells (CD3+δγ−) from rat splenocytes, analyzed by FCM (n = 3 splenic preparations). (d) PEG-HCC internalization in primary CD3+CD4+, TH1-polarized effector memory rat T cells, analyzed by FCM (n = 3 splenic preparations). Mean ± s.e.m. *P < 0.05, **P < 0.01, ***P < 0.001.