Amongst the upregulated genes, the p62 (also known as sequestosome 1) (SQSTM1) is an adaptor protein that has a role in inflammation, neurogenesis, osteoclastogeneis, adipogenesis and T-cell differentiation [21]. Our data indicated that p62 is induced by TLR-2 and NOD-1 activation at both mRNA and protein levels. Elucidating the pathways that control selleck products p62 levels in MSC will add another layer of detail to our understanding of the cell differentiation cascades in which p62

is involved. In addition to p62, VEGF and CXCL-10 were upregulated in response to NOD-1 and TLR-2 signalling. Human MSC released VEGF in response to TLR-2 and NOD-1 ligands as a potentially beneficial paracrine response. It will be interesting to investigate which mechanisms are involved in VEGF upregulation and secretion in MSC. Notably, previous studies have suggested a direct contribution of MSC to the blood vessel formation, as differentiation of MSC

into endothelial cells has been demonstrated [22, 23]. In contrast to NOD-1, TLR-2 signalling Doramapimod also upregulated the expression of several important genes such as interleukin-1 receptor-associated kinase 2 (IRAK-2), involved in TLR signalling, NOTCH-1 and Gal-3 involved in innate and adaptive immunity. Notably, Notch pathway is highly conserved in evolution and is generally involved in cell fate decisions during cell differentiation [24]. A recent study showed that the inhibition of Notch signalling in MSC can hinder their suppressive activity on T-cell proliferation [13]. In addition to binding to glycan structures that are expressed by host cells, galectins can also recognize β-galactoside carbohydrates that are common structures on many pathogens [25], and therefore they are considered as a soluble pathogen recognition receptor. Within

the immune system, galectins are expressed Urease by virtually all immune cells, either constitutively or in an inducible fashion [17]. Also, they can be expressed by a spectrum of normal and tumour cells. As found in this study, Gal-3 is constitutively expressed by MSC and upregulated in response to TLR-2 ligation. Of note, high levels of Gal-3 protein are found in MSC culture supernatants; thus, it may participate in extra cellular matrix (ECM)-cell interactions and modulation of surrounding immune cells. Results from knockdown experiments showed that the immunosuppressive effects of MSC on T cells was lower than that from cells expressing Gal-3, suggesting a possible involvement of Gal-3 in MSC immunosuppressive function. This observation would fit with the demonstrated inhibitory effect of Gal-3 on T-cell proliferation [19, 20]. Also, a more recent study showed that tumour-associated Gal-3 contributes to tumour immune escapes by inhibiting the function of tumour-reactive T cells [26]. Some studies demonstrated that the MSC immunoregulatory properties are at least in part mediated by the production of cytokines, such TGF-β and hepatocyte growth factors [27].