Prenatal and Postnatal Epigenetic Programming: Implications for GI, Immune, and Neuronal Function in Autism
Figure 6
Expression of EAAT3 in CD4+ T-cells from C57BL6/J and SJL/J mice. Spleen and lymph node-derived lymphocytes were separated by FACS analysis cell sorting, followed by qRT-PCR analysis for EAAT3 (EAAC1) expression. EAAT3 expression was significantly higher in CD4+ T-cells from C57BL6/J mice versus autoimmune-prone SJL/J mice ().
