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. 2020 Jul 27;17:224. doi: 10.1186/s12974-020-01899-x

Fig. 3.

Fig. 3

Myelin uptake increases CD36 expression in an NRF2-dependent manner. a, b mRNA expression (n = 9 wells) and surface protein level (n = 4 wells) of CD36 in bone marrow-derived macrophages (BMDMs) treated with vehicle, myelin, and a PPARγ antagonist (GW9662, 10 μM) for 24 h (n = 9 wells). c, d mRNA expression (n = 6 wells) and relative surface protein level (n = 4 wells) of CD36 in wild-type (wt) and Nrf2-deficient (Nrf2−/−) BMDMs treated with myelin or left untreated for 24 h. eg mRNA expression (n = 6 wells) of Ho1, Nqo1, and Nrf2 in wt and Nrf2−/− BMDMs treated with myelin or left untreated for 24 h. MFI, mean fluorescence intensity. Data are represented as mean ± s.e.m. *p < 0.05, **p < 0.01, and ***p < 0.001