IQGAP1 in microbial pathogenesis: Targeting the actin cytoskeleton

被引:36
|
作者
Kim, Hugh [3 ,4 ]
White, Colin D. [2 ,3 ]
Sacks, David B. [1 ]
机构
[1] NIH, Dept Lab Med, Bethesda, MD 20892 USA
[2] Beth Israel Deaconess Med Ctr, Dept Pathol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Boston, MA 02115 USA
[4] Brigham & Womens Hosp, Dept Translat Med, Boston, MA 02115 USA
来源
FEBS LETTERS | 2011年 / 585卷 / 05期
基金
加拿大健康研究院; 美国国家卫生研究院;
关键词
EPEC; IQGAP1; Microbial pathogenesis; Salmonella; ENTEROPATHOGENIC ESCHERICHIA-COLI; EPITHELIAL-CELLS; PLASMA-MEMBRANE; III SECRETION; PHOSPHATIDYLINOSITOL; 3-KINASE; LISTERIA-MONOCYTOGENES; MICROTUBULE DYNAMICS; CAPTURE MICROTUBULES; SIGNAL-TRANSDUCTION; BACTERIAL INVASION;
D O I
10.1016/j.febslet.2011.01.041
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Microbial pathogens cause widespread morbidity and mortality. Central to the pathogens' virulence is manipulation of the host cell's cytoskeleton, which facilitates microbial invasion, multiplication, and avoidance of the innate immune response. IQGAP1 is a ubiquitously expressed scaffold protein that integrates diverse signaling cascades. Research has shown that IQGAP1 binds to and modulates the activity of multiple proteins that participate in bacterial invasion. Here, we review data that support a role for IQGAP1 in infectious disease via its ability to regulate the actin cytoskeleton. In addition, we explore other mechanisms by which IQGAP1 may be exploited by microbial pathogens. Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:723 / 729
页数:7
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