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Rac1、RhoA和Cdc42参与B族链球菌对HeLa细胞的侵袭过程。

Rac1, RhoA, and Cdc42 participate in HeLa cell invasion by group B streptococcus.

作者信息

Burnham Carey-Ann D, Shokoples Sandra E, Tyrrell Gregory J

机构信息

The Department of Laboratory Medicine and Pathology, The University of Alberta, Edmonton, AB, Canada.

出版信息

FEMS Microbiol Lett. 2007 Jul;272(1):8-14. doi: 10.1111/j.1574-6968.2007.00768.x. Epub 2007 May 21.

Abstract

The group B streptococcus (GBS) is an important human pathogen with the ability to cause invasive disease. To do so, the bacteria must invade host cells. It has been well documented that GBS are able to invade a variety of nonphagocytic host cell types, and this process is thought to involve a number of pathogen-host cell interactions. While some of the molecular aspects of the GBS-host cell invasion process have been characterized, many events still remain unclear. The objective of this investigation was to evaluate the role of the Rho-family GTPases Rac, Rho, and Cdc42 in GBS invasion into epithelial cells. The epithelial cell invasion process was modeled using HeLa 229 cell culture. Treatment of HeLa cells with 10 microM compactin, a pan-GTPase inhibitor, abolished GBS internalization, suggesting that GTPases are involved in the GBS invasion process. The addition of Toxin B or exoenzyme C3 to HeLa cells before GBS infection reduced invasion by 50%, further suggesting that the Rho-family GTPases are involved in GBS entry. Examining invasion of GBS into HeLa cells with altered genetic backgrounds was used to confirm these findings; GBS invasion into HeLa cells transiently transfected with dominant negative Rac1, Cdc42, or RhoA reduced invasion by 75%, 51%, and 42%, respectively. Results of this study suggest that the Rho-family GTPases are required for efficient invasion of HeLa cells by GBS.

摘要

B族链球菌(GBS)是一种重要的人类病原体,具有引发侵袭性疾病的能力。为此,该细菌必须侵入宿主细胞。已有充分文献证明,GBS能够侵入多种非吞噬性宿主细胞类型,并且这一过程被认为涉及许多病原体与宿主细胞的相互作用。虽然GBS - 宿主细胞侵袭过程的一些分子层面已得到表征,但许多事件仍不清楚。本研究的目的是评估Rho家族小GTP酶Rac、Rho和Cdc42在GBS侵袭上皮细胞中的作用。使用HeLa 229细胞培养对上皮细胞侵袭过程进行建模。用泛GTP酶抑制剂10微摩尔的康帕丁处理HeLa细胞,消除了GBS的内化,表明小GTP酶参与了GBS侵袭过程。在GBS感染前向HeLa细胞中添加毒素B或外切酶C3使侵袭减少了50%,进一步表明Rho家族小GTP酶参与了GBS的进入。通过检测GBS对具有改变遗传背景的HeLa细胞的侵袭来证实这些发现;GBS对瞬时转染显性负性Rac1、Cdc42或RhoA的HeLa细胞的侵袭分别减少了75%、51%和42%。本研究结果表明,Rho家族小GTP酶是GBS有效侵袭HeLa细胞所必需的。

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