Difference in the expression of TGFb1 in relation to Hp infection, Lauren’s classification, or lymph node involvement. Activated TGF-b1 was abundant in the mucosa of Hp-infected patients, however, there was no significant difference compared to Hp-negative patients [35]. In addition, our results also showed that some stromal cells were stained positive for TGF-b1. Similarly, mononuclear cells in lamina propria were reported to be the major source of TGF-b1 [36]. Comerci et al [37] revealed that TGF-b1 secreted into or produced by supporting stromal order 1948-33-0 elements might indirectly promote tumor progression. Ottaviano et al [38] showed that the crosstalk between cancer cells and stromal elements mediated by TGF-b1 influenced cell surface- and pericellular matrix-degrading Tartrazine web potential in vitro. We therefore conclude that the secretion of TGF-b by tumor cells and stromal cells might play important roles in occurring and maintaining of tumor microenvironment. The results revealed 25331948 that TGF-b was also pronounced in the peripheral system, since the serum concentrations of TGF-b1 and TGF-b2 in GC patients were higher than those in controls.TGF-b Roles in Tumor-Cell Interaction with PBMCsFigure 3. Changes in TGF-b1 and TGF-b2 expression in a coculture model. (A) TGF-b1 and TGF-b2 mRNA levels in GC cells after direct cocultures were increased compared to monoculture, but there were no significant differences in TGF-b1 and TGF-b2 mRNA levels in GC cells, irrespective of the origin of the PBMCs (GC patients or controls). (B) TGF-b1concentrations in the cell supernatant of cocultures were significantly increased compared to those in PBMCs or GCs cultured alone in a FBS-free environment (P,0.05). Its levels in the direct coculture group were significantly higher than those in the indirect group (P = 0.029). TGF-b2 levels were also increased in direct cocultures, but the differences after cocultures were not significant. (C) Cytokine production levels were significantly increased in indirect coculture groups after the addition of FBS (P,0.05), but no obvious change was detected in direct coculture ones. The experiment was conducted twice. All data are shown as means 6 SD of triplicates. (D) Origin of cytokines. In GC cells, TGF-b1 mRNA levels were increased approximately 3-fold in the direct coculture and increased 2-fold in the indirect one compared to monocultures; TGF-b2 mRNA levels were significantly increased after direct coculture but not statistically changed after indirect one. In PBMCs, TGF-b1 mRNA levels were significantly decreased and TGF-b2 levels were remarkably increased after cocultures. Levels were normalized to GAPDH, and levels in the monoculture group were defined as 1.0. All data are shown as means 23977191 6 SD. (E) The mRNA levels of Smad2 and Smad3 in GC cells were significantly increased after cocultures (P,0.05), which were higher in the direct coculture than those in the indirect one,TGF-b Roles in Tumor-Cell Interaction with PBMCsbut there was no statistic difference in the levels of Smad4. (F) Cell-IQ showed that the addition of exogenous TGF-b1 (25 ng/mL) to GC cells suppressed the growth and division of tumor cells, but with no significant difference. Eight images from different visual field were analyzed for each group. (G) Cell Counting Kit-8 (CCK-8) assay showed that TGF-b1 (25 ng/mL) inhibited the viability of PBMCs significantly at 72 h. The line shows the inhibition ratio of TGF-b1 stimulated cells compared to untreated controls. G.Difference in the expression of TGFb1 in relation to Hp infection, Lauren’s classification, or lymph node involvement. Activated TGF-b1 was abundant in the mucosa of Hp-infected patients, however, there was no significant difference compared to Hp-negative patients [35]. In addition, our results also showed that some stromal cells were stained positive for TGF-b1. Similarly, mononuclear cells in lamina propria were reported to be the major source of TGF-b1 [36]. Comerci et al [37] revealed that TGF-b1 secreted into or produced by supporting stromal elements might indirectly promote tumor progression. Ottaviano et al [38] showed that the crosstalk between cancer cells and stromal elements mediated by TGF-b1 influenced cell surface- and pericellular matrix-degrading potential in vitro. We therefore conclude that the secretion of TGF-b by tumor cells and stromal cells might play important roles in occurring and maintaining of tumor microenvironment. The results revealed 25331948 that TGF-b was also pronounced in the peripheral system, since the serum concentrations of TGF-b1 and TGF-b2 in GC patients were higher than those in controls.TGF-b Roles in Tumor-Cell Interaction with PBMCsFigure 3. Changes in TGF-b1 and TGF-b2 expression in a coculture model. (A) TGF-b1 and TGF-b2 mRNA levels in GC cells after direct cocultures were increased compared to monoculture, but there were no significant differences in TGF-b1 and TGF-b2 mRNA levels in GC cells, irrespective of the origin of the PBMCs (GC patients or controls). (B) TGF-b1concentrations in the cell supernatant of cocultures were significantly increased compared to those in PBMCs or GCs cultured alone in a FBS-free environment (P,0.05). Its levels in the direct coculture group were significantly higher than those in the indirect group (P = 0.029). TGF-b2 levels were also increased in direct cocultures, but the differences after cocultures were not significant. (C) Cytokine production levels were significantly increased in indirect coculture groups after the addition of FBS (P,0.05), but no obvious change was detected in direct coculture ones. The experiment was conducted twice. All data are shown as means 6 SD of triplicates. (D) Origin of cytokines. In GC cells, TGF-b1 mRNA levels were increased approximately 3-fold in the direct coculture and increased 2-fold in the indirect one compared to monocultures; TGF-b2 mRNA levels were significantly increased after direct coculture but not statistically changed after indirect one. In PBMCs, TGF-b1 mRNA levels were significantly decreased and TGF-b2 levels were remarkably increased after cocultures. Levels were normalized to GAPDH, and levels in the monoculture group were defined as 1.0. All data are shown as means 23977191 6 SD. (E) The mRNA levels of Smad2 and Smad3 in GC cells were significantly increased after cocultures (P,0.05), which were higher in the direct coculture than those in the indirect one,TGF-b Roles in Tumor-Cell Interaction with PBMCsbut there was no statistic difference in the levels of Smad4. (F) Cell-IQ showed that the addition of exogenous TGF-b1 (25 ng/mL) to GC cells suppressed the growth and division of tumor cells, but with no significant difference. Eight images from different visual field were analyzed for each group. (G) Cell Counting Kit-8 (CCK-8) assay showed that TGF-b1 (25 ng/mL) inhibited the viability of PBMCs significantly at 72 h. The line shows the inhibition ratio of TGF-b1 stimulated cells compared to untreated controls. G.
