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Formation of stress fibres in human endothelial cells infected with Bartonella bacilliformis is associated with altered morphology, impaired migration and defects in cell morphogenesis

机译:细菌芽孢杆菌感染的人内皮细胞中应力纤维的形成与形态改变,迁移受损和细胞形态发生缺陷有关

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Bartonella bacilliformis, a Gram-negative, flagellated bacterium, infects human erythrocytes (haematic phase) and endothelial cells (tissue phase), resulting in a biphasic disease. In the tissue phase of disease (verruga peruana), infection leads to infection of endothelial cells and a pronounced proliferation of these cells, resulting in characteristic skin eruptions of papules and nodules. We have studied the properties of endothelial cells infected in vitro. Extensive cytoskeletal remodelling of endothelial cells occurred after infection in vitro with B. bacilliformis. The cells became spindle shaped and contained arrays of actin stress fibres orientated parallel to the long axis of the cell. Cell-cell contacts were disrupted, along with the distribution of the plasma membrane marker protein, PECAM-1, which participates in cell-cell junctions. The prominent stress fibres terminated in an increased number of focal contacts, which were studied using immunofluorescent staining for paxillin, a cytoplasmic protein that localizes in the focal adhesions. These morphological changes are consistent with activation of intracellular Rho by B. bacilliformis. Formation of stress fibres and the increased number of focal adhesions could be prevented by preincubation of the endothelial cells with C3 exoenzyme, which inactivates intracellular Rho by ADP ribosylation. Endothelial cell motility was greatly diminished in infected cells and the cells did not respond effectively to a stimulus that would evoke motility. In addition, infection of endothelial cells interfered with their ability to form networks of capillary tubes when suspended within three-dimensional collagen matrices. If the properties of infected endothelial cells in vivo are similar, the infected cells will probably not participate effectively in angiogenesis.
机译:革兰氏阴性杆菌是一种鞭毛细菌,它会感染人的红血球(血液阶段)和内皮细胞(组织阶段),从而导致双相性疾病。在疾病的组织阶段(verruga peruana),感染导致内皮细胞感染和这些细胞的明显增殖,导致丘疹和结节出现皮肤特征性爆发。我们已经研究了体外感染的内皮细胞的特性。在体外感染了芽孢杆菌后,内皮细胞发生了广泛的细胞骨架重塑。细胞变成纺锤形,并包含平行于细胞长轴取向的肌动蛋白应力纤维阵列。细胞间的接触以及参与细胞间连接的质膜标记蛋白PECAM-1的分布都被破坏。突出的应力纤维终止于越来越多的焦点接触,使用免疫荧光染色法研究了paxillin(一种定位于粘着斑的细胞质蛋白)。这些形态学变化与芽孢杆菌对细胞内Rho的激活是一致的。可以通过将内皮细胞与C3外切酶预孵育来防止应力纤维的形成和粘着斑数量的增加,C3外切酶通过ADP核糖基化使细胞内Rho失活。在感染的细胞中内皮细胞的运动能力大大降低,并且细胞对引起运动的刺激没有有效反应。另外,当悬浮在三维胶原蛋白基质中时,内皮细胞的感染会干扰它们形成毛细管网络的能力。如果体内被感染的内皮细胞的特性相似,则被感染的细胞可能不会有效参与血管生成。

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