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Escherichia coli Cytotoxic Necrotizing Factor 1 Inhibits Intestinal Epithelial Wound Healing In Vitro after Mechanical Injury

机译:大肠杆菌细胞毒性坏死因子1抑制机械损伤后体外肠上皮伤口愈合。

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摘要

Cytotoxic necrotizing factor type 1 (CNF1) from Escherichia coli activates the small GTP-binding proteins of the Rho family (Rho, Rac, and Cdc42) by catalyzing their deamidation at a specific glutamine residue. Since RhoA, Rac, and Cdc42 play a pivotal role in cell migration during the early phase of wound repair, we investigated whether CNF1 was able to interfere with wound healing in intestinal epithelial monolayers (T84 cells). After mechanical injury, we found that CNF1 blocks epithelial wound repair within 48 h. This effect was characterized by cell elongation and filopodium formation on the leading edge, in association with permanent phosphorylation of the focal adhesion kinase (FAK) via Rho activation. Moreover, inhibition of Rho kinase with Y-27632 decreased CNF1-mediated permanent FAK phosphorylation, leading to complete restitution of wound repair within 24 h. In addition, we found that CNF1 induced upregulation of mitogen-activated protein kinases (MAPK) activation. Moreover, activation of Rac and MAPK by CNF1 increased matrix metalloproteinase 9 expression in wounded T84 monolayers. Taken together, these results provide evidence that CNF1 strongly impairs intestinal epithelial wound healing.
机译:大肠杆菌的细胞毒性坏死因子1型(CNF1)通过在特定的谷氨酰胺残基处催化脱酰胺作用,激活了Rho家族的小GTP结合蛋白(Rho,Rac和Cdc42)。由于RhoA,Rac和Cdc42在伤口修复的早期阶段在细胞迁移中起着关键作用,因此我们研究了CNF1是否能够干扰肠上皮单层(T84细胞)中的伤口愈合。机械损伤后,我们发现CNF1在48小时内阻断了上皮伤口的修复。这种作用的特征是细胞伸长和前端的假单胞菌形成,以及通过Rho激活引起的粘着斑激酶(FAK)的永久磷酸化。此外,用Y-27632抑制Rho激酶可减少CNF1介导的永久FAK磷酸化,从而在24小时内完全恢复伤口修复。此外,我们发现CNF1诱导有丝分裂原激活的蛋白激酶(MAPK)激活的上调。此外,CNF1对Rac和MAPK的激活增加了受伤T84单层中基质金属蛋白酶9的表达。综上所述,这些结果提供了证据,表明CNF1严重损害了肠上皮伤口的愈合。

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