We analyzed T-cell subpopulations in Pim1TgγcKO LN and spleen, but found that neither γδ T cells, CD25+FoxP3+ Treg-cells, or NKT cells
were recovered (Fig. 5A–C). Also, CD8α+ IELs were drastically reduced and the IL-15-dependent CD8αα IEL population was completely absent (Fig. 5D), suggesting a nonredundant role of γc cytokines in generation and maintenance of these cells. We also failed to observe any γδ T cells in the IEL population (Fig. 5E). Altogether, Pim1 was sufficient to restore peripheral CD4+ αβ T-cell numbers and to improve CD8+ T-cell survival in the absence of γc. However, it was insufficient to restore other T-lineage selleck chemical cells, including γδ T cells, NKT cells, CD8αα IELs, and FoxP3+ Treg cells. Thus, CD4+ T cells are unique in that Pim1-mediated survival effect was sufficient to meet their γc signaling requirement. To understand the extent to which Pim1 can replace the γc requirement, we analyzed Pim1TgγcKO LN T cells in further detail. We found that all LN T cells had downregulated IL-7R-α and CD103 expression that resembles
an activated/memory phenotype (Fig. 6A). In agreement, most Pim1TgγcKO CD4+ and CD8+ T cells expressed high levels of the memory marker CD44 (Fig. 6B). Thus, Pim1 promotes T-cell survival in the absence of γc, but it fails to maintain a naïve T-cell pool. Interestingly, surface CD8 see more protein levels on Pim1TgγcKO CD8+ T cells were significantly lower than on WT CD8+ T cells (Fig. 6C). Since in vivo CD8 surface and mRNA levels are determined by IL-7 signaling , reduced CD8 surface and mRNA levels suggested that Pim1 cannot replace the CD8 regulatory arm of γc signaling (Fig. 6C and Supporting Information Fig. 3D). Along this line, we found that expression of the CD8 lineage specifying factor Runx3, but not Runx1, was significantly reduced in Pim1TgγcKO CD8+ T cells (Supporting Information Fig. 3D). Taken together, these data indicate that Pim1 is limited in its ability to replace in vivo effects of γc signaling, and that additional γc signaling pathways are necessary to maintain CD8+ T-cell homeostasis. To test whether γc signaling is
required for Th function, next we analyzed surface CD40L expression on activated Pim1TgγcKO CD4+ T cells. Thiamine-diphosphate kinase Overnight TCR stimulation upregulated CD5 and CD40L expression on both WT and Pim1TgγcKO CD4+ T cells (Fig. 6D). CD40L expression was CD4+ T-cell specific since activated CD8+ T cells failed to express CD40L (Supporting Information Fig. 3E). These results indicate that CD4+ Th function can be acquired in the absence of γc. On the other hand, Th lineage differentiation was dependent on γc signaling. Stimulation of Pim1TgγcKO CD4+ T cells under Th1 or Th2 cell differentiating conditions failed to produce Th1 or Th2 cells based on intracellular IFN-γ and IL-4 expression, respectively (Fig. 6E). However, IL-17a producing Th17-cell differentiation, which is mediated by the non-γc cytokines IL-6 and TGF-β, was intact in Pim1TgγcKO CD4+ T cells (Fig. 6E, bottom).