The presence of several glycolytic enzymes in PCM and not in BCM supports the notion that central metabolic processes are in different states in find more planktonic and biofilm cultures and that those different metabolic states likely have a large impact on the observed pathogenic effects on HKs described here. Functional annotation clustering of upregulated transcripts revealed over-represented annotation

clusters associated with response to bacteria, regulation of transcription, inflammation, and signal transduction (Figure 2). The gene ontology term mTOR inhibitor review “”response to glucocorticoid stimulus”" was interesting as glucocorticoids are anti-inflammatory hormones. Genes involved in cyclic adenosine monophosphate (cAMP) signaling were also interesting since cAMP is involved in several fundamental cellular processes and may be partially responsible for the observed effects induced by BCM. Functional annotation clustering of downregulated

transcripts revealed over-represented annotation clusters associated with transcription and metabolism. The downregulation of genes associated with these processes may indicate a general cessation in BCM treated cells. Transcriptional responses of HKs to BCM revealed the upregulation of pro-inflammatory genes, including transcripts for pro-inflammatory transcription factors, cytokines, and apoptosis related genes. Among these were members of the AP-1 family of transcription factors and regulators of the NFkB pro-inflammatory transcription factor, TNFAIP3 (A20) and NFkBIA. Expression of these genes indicated active regulation of the NFkB pathway. NFkB regulates the expression this website of many

genes involved in immune and inflammatory responses (i.e. cytokine and chemokine genes) and often acts in synergy with AP-1 to mediate inflammatory responses [33, 34]. NFkB and AP-1 are activated by pro-inflammatory cytokines such as TNF-α and IL-1β which act through MAPK-dependent signal cascades resulting in the production of additional cytokines [35–38]. The transcription factor egr1, which was highly upregulated 3-mercaptopyruvate sulfurtransferase in BCM treated HKs, is also involved in the regulation of pathophysiologically important genes relating to inflammation, apoptosis, and differentiation [39–41]. The upregulation of these early response transcription factors indicates that four hours of treatment with BCM induces a swift inflammatory response in HKs relative to PCM. We previously investigated BCM induced apoptosis and HK migration in a scratch wound model [20]. In agreement with that study, S. aureus BCM induced apoptosis in HKs while PCM did not induce a significant amount of apoptosis. BCM mediated induction of apoptosis is discussed in detail in [20]. This striking dissimilarity between PCM and BCM would undoubtedly have substantial impacts on several aspects of wound healing. Cytokine production induced by PCM and BCM were normalized to adherent non-apoptotic HKs.