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. 2018 Sep 24;1(5):e201800039. doi: 10.26508/lsa.201800039

Figure 4. Proliferation and cytokine production in MOG35–55 immunized WT and HDAC11 KO mice.

Figure 4.

(A) Mice were immunized at the base of the tail, and lymph nodes were harvested 11 d later. Cells were cultured with increasing concentrations of MOG35–55 peptide for 72 h and pulsed with thymidine during the last 14 h of culture. Stimulation index is calculated by dividing mean counts per minute ± SD of stimulated cells cultured with peptide to mean counts per minute ± SD of unstimulated cells cultured without peptide (n = 6). (B, C) Mice were immunized at two sites on the back, and spleens were harvested and cultured with 20 μg MOG35–55 for 48 h. Supernatants were analyzed for cytokine production. Data shown are mean ± SD from three independent animals per genotype, *P < 0.05. (D) Mice were immunized with MOG35–55, mRNA was extracted from the lumbar region of the spinal cords at the indicated time post immunization (P.I.), and CCL2 mRNA expression was quantified by qPCR. Data shown are mean ± SD from three independent animals per genotype, of three independent experiments, and P-values were calculated by t test, *P < 0.05.