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• W1495294520 abstract "Salmonella enterica Typhimurium induces intestinal inflammation through the activity of type III secreted effector (T3SE) proteins. Our prior results indicate that the secretion of the T3SE SipA and the ability of SipA to induce epithelial cell responses that lead to induction of polymorphonuclear transepithelial migration are not coupled to its direct delivery into epithelial cells from Salmonella. We therefore tested the hypothesis that SipA interacts with a membrane protein located at the apical surface of intestinal epithelial cells. Employing a split ubiquitin yeast-two-hybrid screen, we identified the tetraspanning membrane protein, p53 effector related to PMP-22 (PERP), as a SipA binding partner. SipA and PERP appear to have intersecting activities as we found PERP to be involved in proinflammatory pathways shown to be regulated by SipA. In sum, our studies reveal a critical role for PERP in the pathogenesis of S. Typhimurium, and for the first time demonstrate that SipA, a T3SE protein, can engage a host protein at the epithelial surface." @default.
• W1495294520 created "2016-06-24" @default.
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• W1495294520 date "2015-01-24" @default.
• W1495294520 modified "2023-10-02" @default.
• W1495294520 title "PERP, a host tetraspanning membrane protein, is required for<scp><i>S</i></scp><i>almonella</i>‐induced inflammation" @default.
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• W1495294520 doi "https://doi.org/10.1111/cmi.12406" @default.
• W1495294520 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4915744" @default.
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