Shin Sooan, Kim Kwang Sik
Division of Pediatric Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
Biochem Biophys Res Commun. 2006 Jun 23;345(1):538-42. doi: 10.1016/j.bbrc.2006.04.130. Epub 2006 May 2.
Type III group B streptococcus (GBS) has been shown to invade human brain microvascular endothelial cells (HBMEC), which constitute the blood-brain barrier, but the underlying mechanisms remain incompletely understood. In the present study, we showed that the geranylgeranyl transferase I inhibitor, GGTI-298, not the farnesyltransferase inhibitor, FTI-277 inhibited type III GBS invasion of HBMEC. The substrates for GGTI-298 include Rho family GTPases, and we showed that RhoA and Rac1 are involved in type III GBS invasion of HBMEC. This was shown by the demonstration that infection with type III GBS strain K79 increased the levels of activated RhoA and Rac1 and GBS invasion was inhibited in HBMEC expressing dominant-negative RhoA and Rac1. Of interest, the level of activated Rac1 in response to type III GBS was decreased in HBMEC expressing dominant-negative RhoA, while the level of activated RhoA was not affected by dominant-negative Rac1. These findings indicate for the first time that activation of geranylgeranylated proteins including RhoA and Rac1 is involved in type III GBS invasion of HBMEC and RhoA is upstream of Rac1 in GBS invasion of HBMEC.
B族链球菌III型(GBS)已被证明可侵入构成血脑屏障的人脑微血管内皮细胞(HBMEC),但其潜在机制仍未完全了解。在本研究中,我们发现香叶基香叶基转移酶I抑制剂GGTI-298而非法尼基转移酶抑制剂FTI-277可抑制GBS III型对HBMEC的侵袭。GGTI-298的底物包括Rho家族GTP酶,我们发现RhoA和Rac1参与GBS III型对HBMEC的侵袭。这通过以下证明得以体现:GBS III型菌株K79感染可增加活化的RhoA和Rac1水平,且在表达显性阴性RhoA和Rac1的HBMEC中GBS侵袭受到抑制。有趣的是,在表达显性阴性RhoA的HBMEC中,对GBS III型反应的活化Rac1水平降低,而活化的RhoA水平不受显性阴性Rac1的影响。这些发现首次表明,包括RhoA和Rac1在内的香叶基香叶基化蛋白的激活参与GBS III型对HBMEC的侵袭,且在GBS对HBMEC的侵袭中RhoA位于Rac1的上游。