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小GTP酶在克氏锥虫侵袭MDCK细胞系中的作用。

Role of small GTPases in Trypanosoma cruzi invasion in MDCK cell lines.

作者信息

Dutra J M F, Bonilha V L, De Souza W, Carvalho T M U

机构信息

Laboratório de Ultraestrutura Celular Hertha Meyer, Instituto de Biofísica Carlos Chagas Filho-CCS-UFRJ-Ilha do Fundão, 21940-900, Rio de Janeiro, Brazil.

出版信息

Parasitol Res. 2005 Jun;96(3):171-7. doi: 10.1007/s00436-005-1333-7. Epub 2005 Apr 30.

Abstract

Trypanosoma cruzi can modulate a large number of host intracellular responses during its invasion. GTPases such as RhoA, Rac1 and Cdc42 are examples of molecules that could be activated at this moment and trigger changes in the pattern of F-actin cytoskeleton leading to the formation of structures like stress fibers, lamellipodium and fillopodium, respectively. Here we investigate the role of these GTPases in the cytoskeletal rearrangement of MDCK cell transfectants expressing variants of RhoA, Rac1 and Cdc42 during T. cruzi infection. The adhesion, internalization and the survival rate were determined. Rac1 mutants showed the higher adhesion and internalization indexes but the lower survival index after 48 h of infection. Confocal laser scanning microscopy showed changes in the pattern of F-actin distribution and reorganization at the site of trypomastigote invasion. These observations suggest that these GTPases act in the signaling mechanisms that affect the F-actin cytoskeleton during T. cruzi invasion.

摘要

克氏锥虫在入侵过程中可调节大量宿主细胞内反应。诸如RhoA、Rac1和Cdc42等小G蛋白是此时可能被激活的分子实例,它们分别触发F-肌动蛋白细胞骨架模式的变化,导致形成应力纤维、片状伪足和丝状伪足等结构。在此,我们研究了这些小G蛋白在克氏锥虫感染期间对表达RhoA、Rac1和Cdc42变体的MDCK细胞转染子细胞骨架重排中的作用。测定了其黏附、内化和存活率。Rac1突变体在感染48小时后显示出较高的黏附和内化指数,但存活率较低。共聚焦激光扫描显微镜显示,在锥鞭毛体入侵部位,F-肌动蛋白分布和重组模式发生了变化。这些观察结果表明,这些小G蛋白在克氏锥虫入侵期间影响F-肌动蛋白细胞骨架的信号传导机制中发挥作用。

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