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. 2021 Jul 13;11:14396. doi: 10.1038/s41598-021-93831-3

Figure 5.

Figure 5

Production of inflammatory cytokines induced by arginase inhibitor diminished by co-culture with peripheral CD71+ erythroid cells derived from SoJIA patient. (a) Upregulated and downregulated genes in PBCECs compared to control neonatal cord blood. (b) Gene expression of ARG2 in CD71+ erythroid cells and CD45+ lymphocytes and monocytes extracted from mononuclear cells in peripheral blood of SoJIA patients and neonatal cord blood. (c, d) The levels of (c) interleukin-1β and (d) interleukin-6 in the culture supernatant after stimulation with lipopolysaccharide at 0, 10, and 100 ng/mL. Healthy donor monocytes are cultured without (left graph) or with PBCECs obtained from SoJIA patients at ratios of 1:0, 1:2, and 1:4 (right graph). ABH was added to the culture medium at 0, 30, and 90 μM. The experiment was repeated three times using PBCECs derived from three different patients, and each culture was performed in triplicate. Data are representative of three independent experiments. Data were represented as the mean ± SD and analyzed by the Mann–Whitney U test with Bonferroni correction. *P < 0.05; **P < 0.01; ***P < 0.001. CB cord blood, PB peripheral blood, LPS lipopolysaccharide, Mo: E ratio mixture ratio of healthy monocytes and patient-derived peripheral CD71+ erythroid cells, ABH amino-2-borono-6-hexanoic acid.