Figure 5 Effect of MSCs on T cell apoptosis. Flk-1+CD31-CD34- MSCs at 1:10 ratios (MSCs to T cells); the data are expressed as mean ± S.D. of triplicates of five separate experiments with similar results. The test was conducted by Annexin-V and PI double staining and analyzed by flow cytometry. Apoptosis of T cells was analyzed in T cells alone (Ts), normalMSC coCUDC-907 clinical trial cultured with activated T cells (MSC + Ts), and CML patient-derived MSC cocultured with activatedT cells (CMLMSC + Ts). Annexin V+means the cells were PI negative and Annexin V positive. Data are shown as means ± S.D. of five independent CP-690550 molecular weight experiments (*p < 0.05 vs. Ts) Efficient extinction of

MMP-9 expression in HT1080 cells by RNAi strategy and the concomitantly upregulation of s-ICAM-1 We used an RNAi method to target MMP-9 in the CML MSC and the constructs we designed encoded an RNA that targets the MMP-9 mRNA. The target sequence had no homology with other members of the MMP family. The ds-RNA and Silencer negative control si-RNA (snc) were each tested for their ability to suppress MMP-9 specifically. We first TH-302 in vitro assessed whether RNAi was dose and time-dependent. A MMP-9 dependent ds-RNA-mediated inhibition was observed in a dose and time dependent manner (Figure 6A). The time-course assay performed with 20 nM ds-RNA-transfected CML MSC showed that the induced MMP-9 silencing could be maintained for at least 3 days (Figure

6B). Besides, serum ICAM-1 was concomitantly changing with MMP-9. The Western blotting results were confirmed by enzyme-linked immunoadsorbent assay. CML

snc-RNA-transfected cells cultured up to 3 days spontaneously released high amount of MMP-9 into the culture conditioned medium whereas ds-RNA-transfected cells showed a marked time- and dose- dependent inhibition in MMP-9 protein levels. Importantly, levels of s-ICAM-1 were also affected with ds-RNA transfection (Figure 6C). Figure 6 Efficient inhibition of MMP-9 in CML MSC using RNAi. (A) The cDNAs from snc-RNA (20 nM) and ds-RNA (1-20 nM) cells cultured for up 3 days were used as templates for PCR reactions using specific primers for MMP-9 and ICAM-1. (B) The cDNAs from snc-RNA (20 nM) and ds-RNA (20 nM) cells cultured for up 4 days were used as templates for PCR reactions using specific selleckchem primers for MMP-9 or 18 S ribosomal RNA. (C) MMP-9 and s-ICAM-1 production (ng/ml) in the culture supernatants of CML snc-RNA (20 nM) or ds-RNA (1-20 nM) cells were determined by enzymelinked immunosorbent assays. Discussion MSC isolated from different tissues had immune regulation ability not only in vivo but in vitro and it might consist the “”immune protection site”" in human body[25, 26]. Considering their richness in source, availability for expansion, and most importantly, their robust immuno-modulatory activity, MSCs appear to be a primary candidate for cellular therapy in immune disorders[12, 16, 27].