Prenatal and Postnatal Epigenetic Programming: Implications for GI, Immune, and Neuronal Function in Autism
Figure 3
Expression of EAAT3 in murine lymphocyte subsets. Spleen and lymph node-derived lymphocytes were separated by magnetic cell sorting, followed by qRT-PCR analysis for EAAT3 (EAAC1) expression. (a) EAAT3 expression was significantly higher () in CD4+ T cells as compared to unseparated lymphocytes (UNSEP), CD8+ T cells, or B cells. (b) EAAT3 expression was significantly higher () in FoxP3+ Treg cells.
