Aepfelbacher M, Heesemann J
Max-von-Pettenkofer Institut für Hygiene und Medizinische Mikrobiologie, München, Germany.
Int J Med Microbiol. 2001 Sep;291(4):269-76. doi: 10.1078/1438-4221-00130.
Pathogenic species of the genus Yersinia employ a type III secretion apparatus to inject up to six effector proteins (Yersinia outer proteins; Yops) into host cells. Thereby yersiniae disarm the immune cell system of the host to proliferate extracellularly. At least four of the Yop effectors (YopE, YpkA/YopO, YopT and YopH) are involved in the rearrangement of the actin cytoskeleton: YopE, YopT and YpkA/YopO modulate the activity of actin-regulating Rho GTP-binding proteins, whereas YopH dephosphorylates phospho-tyrosine residues in focal adhesion proteins. In this review we will focus on recent evidence implicating Rho GTPases and the actin cytoskeleton as major targets of Yersinia Yops.
耶尔森氏菌属的致病菌种利用III型分泌装置将多达六种效应蛋白(耶尔森氏菌外蛋白;Yops)注入宿主细胞。由此,耶尔森氏菌解除宿主免疫细胞系统的武装,以便在细胞外增殖。至少四种Yop效应蛋白(YopE、YpkA/YopO、YopT和YopH)参与肌动蛋白细胞骨架的重排:YopE、YopT和YpkA/YopO调节肌动蛋白调节Rho GTP结合蛋白的活性,而YopH使粘着斑蛋白中的磷酸酪氨酸残基去磷酸化。在本综述中,我们将聚焦于近期的证据,这些证据表明Rho GTP酶和肌动蛋白细胞骨架是耶尔森氏菌Yops的主要靶点。