Ne induced ZO-1 internalization. And morphine enhanced LTA’s effects on

Ne induced ZO-1 internalization. And morphine enhanced LTA’s effects on IEC-6 cells, further validating that TLR2 plays a more dominant role in TJ modulation in gut epithelial cells following morphine treatment. In contrast, neither LPS nor LTA showed any effect on TJ distribution in colonic CMT-93 cells, consistent with our in vivo data (Figure S4).TLR signaling modulates intestinal tight junction organization in a MLCK-dependent mannerSince our data (Figure S2) show that TLR ligands have no effect on tight junction protein expression levels, the increased permeability of epithelial cells by TLR activation may involve posttranslation mechanisms. Recent studies showed that myosin lightchain kinase (MLCK) regulates the contraction of tight junctions by phosphorylating myosin light chains [24,33,34]. Activation of MLCK induces phosphorylation of the myosin light chains, resulting in the contraction of cytoskeleton proteins such as F-actin and thus inducing the GKT137831 site internalization of associated tight junction proteins such as GSK0660 occludin and ZO-1. To determine whether MLCK is responsible, we determined the barrier function of IEC6 cells by electrical cell impedance sensing (ECIS) arrays. The cells were grown to confluence in ECIS arrays, and the trans-epithelial resistance (TER) values were measured to test whether morphine would affect epithelial barrier integrity. The baseline TER of each experiment was normalized to 1.0 to enable comparison and statistical analysis of TER changes over time following different treatments. IEC-6 cells were treated with MLCK inhibitor ML-7, and the TER values were measured in the presence of LTA (Figure 7A) and LPS (Figure 7B). Inhibition of MLCK restored the TER values to the control levels, indicating that the effects of TLR agonists on epithelial cells are dependent on MLCK. To further validate the role of MLCK in tight junction modulation, WT mice were injected with 2 mg of ML-7/kg body weight prior to morphine treatment as described previously [24]. ML-7 inhibitedMorphine Promotes Bacterial TranslocationFigure 6. TLR2/TLR4 knockout protects tight junction organization from morphine-induced disruption. (A) Occludin organization in small intestine of WT and TLRKO mice. (B) ZO-1 organization in small intestine of WT and TLRKO mice. WT, TLR2 knockout, TLR4 knockout, and TLR2/4 double knockout mice were implanted with 75 mg morphine pellet for 24 hours. The similar parts of small intestines were excised and fixed. Images were analyzed by confocal scanning microscope. (n = 5) Scale bar: 10 mm. doi:10.1371/journal.pone.0054040.gmorphine-induced bacterial translocation to MLN and liver (Figure 7C), and protected occludin and ZO-1 organization from morphine-induced disruption (Figure 7D), although it did not block constipation caused by morphine treatment (Figure S3).DiscussionIn the current study, we show that morphine mediated signaling by m-opioid receptors 1) induced bacterial dissemination into MLN and liver of WT mice; 2) compromised intestinal barrier function; and 3) disrupted tight junction organization in gut epithelial cells through a TLR- dependent mechanism. Our studies show significant bacterial translocation to the mesenteric lymph node and liver of WT mice that are morphine treated (Figure 1A and Figure S1). Over the past two decades, a large amount of studies have been conducted to investigate the effects of morphine on bacterial translocation and intestinal permeability using various rodent models.Ne induced ZO-1 internalization. And morphine enhanced LTA’s effects on IEC-6 cells, further validating that TLR2 plays a more dominant role in TJ modulation in gut epithelial cells following morphine treatment. In contrast, neither LPS nor LTA showed any effect on TJ distribution in colonic CMT-93 cells, consistent with our in vivo data (Figure S4).TLR signaling modulates intestinal tight junction organization in a MLCK-dependent mannerSince our data (Figure S2) show that TLR ligands have no effect on tight junction protein expression levels, the increased permeability of epithelial cells by TLR activation may involve posttranslation mechanisms. Recent studies showed that myosin lightchain kinase (MLCK) regulates the contraction of tight junctions by phosphorylating myosin light chains [24,33,34]. Activation of MLCK induces phosphorylation of the myosin light chains, resulting in the contraction of cytoskeleton proteins such as F-actin and thus inducing the internalization of associated tight junction proteins such as occludin and ZO-1. To determine whether MLCK is responsible, we determined the barrier function of IEC6 cells by electrical cell impedance sensing (ECIS) arrays. The cells were grown to confluence in ECIS arrays, and the trans-epithelial resistance (TER) values were measured to test whether morphine would affect epithelial barrier integrity. The baseline TER of each experiment was normalized to 1.0 to enable comparison and statistical analysis of TER changes over time following different treatments. IEC-6 cells were treated with MLCK inhibitor ML-7, and the TER values were measured in the presence of LTA (Figure 7A) and LPS (Figure 7B). Inhibition of MLCK restored the TER values to the control levels, indicating that the effects of TLR agonists on epithelial cells are dependent on MLCK. To further validate the role of MLCK in tight junction modulation, WT mice were injected with 2 mg of ML-7/kg body weight prior to morphine treatment as described previously [24]. ML-7 inhibitedMorphine Promotes Bacterial TranslocationFigure 6. TLR2/TLR4 knockout protects tight junction organization from morphine-induced disruption. (A) Occludin organization in small intestine of WT and TLRKO mice. (B) ZO-1 organization in small intestine of WT and TLRKO mice. WT, TLR2 knockout, TLR4 knockout, and TLR2/4 double knockout mice were implanted with 75 mg morphine pellet for 24 hours. The similar parts of small intestines were excised and fixed. Images were analyzed by confocal scanning microscope. (n = 5) Scale bar: 10 mm. doi:10.1371/journal.pone.0054040.gmorphine-induced bacterial translocation to MLN and liver (Figure 7C), and protected occludin and ZO-1 organization from morphine-induced disruption (Figure 7D), although it did not block constipation caused by morphine treatment (Figure S3).DiscussionIn the current study, we show that morphine mediated signaling by m-opioid receptors 1) induced bacterial dissemination into MLN and liver of WT mice; 2) compromised intestinal barrier function; and 3) disrupted tight junction organization in gut epithelial cells through a TLR- dependent mechanism. Our studies show significant bacterial translocation to the mesenteric lymph node and liver of WT mice that are morphine treated (Figure 1A and Figure S1). Over the past two decades, a large amount of studies have been conducted to investigate the effects of morphine on bacterial translocation and intestinal permeability using various rodent models.