(B) IDO gene integration and transcription by PCR and RT-PCR. (C) Western blot analysis of IDO protein expression in CHO-IDO cells using anti-IDO antibody. In transfected group, CHO cells transfected with IDO expressed the 42 kDa IDO protein, indicating that CHO cells stably transfected with IDO could produce IDO protein. (D) Analysis of free amino acids in culture
supernatant. Amino acid level in CHO cells 72 h after IDO transfection: (His) 33.75 mg/L, (Kyn) 7.03 mg/L, (Trp) < 3 pmol. Amino acid level in CHO cells with pIRES2-EGFP transfection 72 h after culturing: (His) 38.12 mg/L, (Trp) 5.63 mg/L, (Kyn) < 3 pmol. His: histidine; Trp: trytophan; Kyn: kynurenine. Effect of IDO+ CHO cells on CD3+T cell find more apoptosis After 72 h of co-culture PF-02341066 order of CD3+T cells and IDO+ CHO selleck chemicals cells, 79.07 ± 8.13% of CD3+T cells were apoptotic compared with 59.80 ± 11.46% of CD3+ T cells co-cultured with CHO/EGFP cells, and 32.40 ± 6.40% of CD3+ T cells that were cultured alone. The differences were statistically significant (P < 0.05), indicating that IDO+ CHO cells could induce significant T cell apoptosis. Furthermore, after added the 1-MT, the specific inhibitor of IDO in co-culture of CD3+T cells and IDO+ CHO cells, the apoptosis could not be induced (only 33.1 ± 4.87% of CD3+T cells were apoptotic) (Figure 2). Figure 2 Effect of IDO + CHO cells
on CD3 + T cell apoptosis. (A) Representative FACS Immune system scatter plots of CD3+T cells apoptosis 72 h after culture with 200 U/ml human recombinant IL-2. (B) Representative FACS scatter plots of CD3+T cells apoptosis 72 h after co-culture with CHO/EGFP cells. (C) Representative FACS scatter plots of apoptotic CD3+T cells 72 h after co-culture with CHO cells transfected with IDO. (D) Representative FACS scatter plots of apoptotic CD3+T cells 72 h after co-culture with CHO cells transfected with IDO and inhibitor 1-MT. (Q4 region represents cells
in the early process of apoptosis; P5 represents the total population of apoptotic CD3+T cells) (E) Relative percentages of apoptotic cells (Annexin V positive and PI negative cells). The columns showed the average (%) ± SD from 3 independent experiments. The differences were statistically significant (P < 0.05), indicating that CHO cells with IDO transfection can significantly induce apoptosis in T cells. In vitro induction of peripheral CD4 + CD25 + CD127- T cells by IDO+ CHO cells in the peripheral blood of breast cancer patients Mononuclear cells isolated from the peripheral blood of breast cancer patients were incubated with IDO+ CHO cells to assess the effect of IDO expression on Treg cells. After 7 days of incubation of 2 × 106 CD3+ T cells in media containing 200 U/ml IL-2, CD4+CD25+CD127- Tregs were 3.43 ± 1.07% of the CD3+T cell population. However, after 7 days of co-culture of 1 × 105 CHO cells expressing IDO or EGFP and 2 × 106 CD3+ T cells, CD4+CD25+CD127- Tregs were 8.98 ± 1.