amazonensis-induced parasitophorous vacuoles in both BALB/c and CBA macrophages. Comparison of differential gene expression by C57BL/6 and CBA macrophages in response to L. amazonensis infection To gain deeper insight into the differences between the respective responses of C57BL/6 and CBA macrophages to infection, the authors attempted to identify specific genes observed to be significantly modulated

in a divergent pattern as a result of L. amazonensis infection. However, the baseline gene expression signatures measured prior to infection present a challenge to this TPX-0005 type of analysis, as inherent transcriptomic differences may interfere with the accurate identification of differentially expressed gene sets. Firstly, all gene expression values were normalized by subtracting the expression levels by infected macrophages from the corresponding mean expression levels (log2-scale) by uninfected cells within a given mouse strain. Thereafter, a direct comparison of normalized gene expression levels was performed using SAM Tideglusib nmr analysis to identify the genes that were differentially expressed between these two mouse strains. Finally, IPA® was used to highlight possible connections between C57BL/6 and CBA macrophages responses to L. amazonensis infection. Networks were constructed from the total number of differentially expressed genes

(n = 114), considering both strains of click here mice. The cell cycle network (See Additional file 6: Figure S2) had the highest probability of interrelated genes being modulated together. This network contains of 35 genes (score 36), with 16

out of the 114 genes that were modulated by either C57BL/6 or CBA macrophages in response to L. amazonensis. Ten of the 16 modulated genes encode proteins involved in several cellular processes: usp3, which encodes an enzyme involved in ubiquitination; phb and polr2a, which encode proteins implicated in the transcription process; elf4b, involved in the translational process; gstp1, which participates in detoxification; rps6ka1 and sipa1, both involved in cellular signaling; cd72, s1pr2 and ptafr, which encode surface receptors. Of these, cd72, s1pr2 and ptafr were found to be up-regulated in C57BL/6 macrophages infected with L. amazonensis (data not shown). These genes encode receptors, which are expressed on macrophage surfaces. Moreover, the modulation of these receptors and subsequent down-regulation of the macrophage proinflammatory response has been previously described [46, 47] and is in accordance with the ability of C57BL/6 macrophages to control L. amazonensis infection [3]. Cd72 has been described as a costimulatory molecule found to be up-regulated in macrophages during the activation of a Th1-type immune response [48].