Figure 4 Adhesion abilities of E. coli to HEp-2 cells. (A) Adhesion of FITC-conjugated ET2, and ET3 to HEp-2 cells. The adhesion ability is expressed as the ratio of florescence from adherent bacteria to that from inoculated bacteria. Bacteria were treated with proteinase K before FITC conjugation. Data represent means of five experiments with triplicate samples in each experiment. ET2, E. coli expressing vector only. ET3, AZD5153 purchase E. coli expressing Scl1. (B) SDS-PAGE and western blot analysis of purified recombinant Scl1 protein. Lane 1 indicates the SDS-PAGE of purified rScl1. Lane 2 indicates the purified rScl1 protein confirmed by western blot analysis using anti-Scl1 antibody. rScl1 is indicated by a
48 kDa band. (C) Inhibition of binding by rScl1 protein and anti-Scl1 antibody. Prior to the adhesion assay, HEp-2 cells were QNZ purchase pre-treated with rScl1 protein and ET3 were pre-treated with anti-Scl1 antibody and mouse IgG, respectively. **, P < 0.01 and ***, P < 0.001. To directly address the role of Scl1 in the binding process, we performed
competition studies using anti-Scl1 antibodies and recombinant Scl1 (rScl1) protein. Polyclonal anti-Scl1 antibodies were generated in 4-week-old BALB/c mice. The full-length rScl1 protein containing sequences shown in Figure 1A was generated and confirmed by SDS-PAGE as a single band of approximately 48 kDa (Lane 1, Figure 4B) and by Florfenicol western blot analysis with anti-Scl1 antibodies (Lane 2, Figure 4B). Both pre-incubation of HEp-2 cells with rScl1 and pre-incubation of ET3 bacteria with anti-Scl1 antibodies significantly blocked the adherence of E. coli ET3 to human epithelial cells (Figure 4C). The adherence of E. coli ET3 to HEp-2 cells was not affected by pre-incubation of ET3 bacteria with non-specific mouse IgG. These results reveal both the importance and sufficiency of Scl1 in mediating the adherence of bacteria to human epithelial cells. Adherence through protein receptor(s) on epithelial cells Our previous
data showed that the adhesion was affected when Scl1-expressed E. coli was pre-incubated with proteinase K, suggesting that the adhesion is mediated through a protein-like molecule on the bacteria. To further determine the corresponding side of surface molecules on epithelial cells mediating this binding process, HEp-2 cells were treated with pronase and phospholipase A2 to Dasatinib modify the protein and lipid contents on the cell membrane, respectively [19]. Treatment of pronase significantly inhibited the binding of ET3 to epithelial cells in a dose-dependent manner (Figure 5A). In contrast, treatment of phospholipase A2 did not affect the binding of ET3 to epithelial cells (Figure 5A). These results suggest that a protein receptor for Scl1 on epithelial cells is likely to mediate this binding event. Figure 5 Adherence through protein receptors on HEp-2 cells. (A) Adhesion of E.
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