Proteomic approach to identify mediators of PI3K activation by P. aeruginosa

描述（由申请人提供）：微生物病原体克服正常高度极化的宿主粘膜上皮屏障的能力是发病机制的早期和关键步骤。这是特别关键的机会致病菌，如铜绿假单胞菌（PA），其中一个最致命的机会致病菌的man. In设置上皮损伤和细胞极性的损失PA可以有效地殖民的粘膜表面，造成进一步的损害，并传播。我们最近发现PA与培养的上皮细胞的顶端（AP）表面的结合诱导细胞重编程过程，其中局部质膜从顶端（AP）转变为基底外侧（BL）膜，产生促进细菌定植和进入上皮细胞的微环境。我们已经通过大量的证据证明，磷酸肌醇3-激酶（PI 3 K）的激活是这一过程中的关键步骤。一个尚未解决的非常重要的问题是，结合后激活的信号通路是什么，导致细菌摄取和创造这种新的微环境。PI 3 K适于接受来自蛋白酪氨酸激酶或酪氨酸磷酸化蛋白的调节输入。已知上皮细胞的PA感染诱导宿主蛋白质的酪氨酸磷酸化状态的变化。我们假设PA感染上皮细胞引起酪氨酸磷酸化信号级联反应，导致PI 3 K的激活。我们的长期目标是了解PA如何与宿主细胞相互作用并导致疾病。我们的短期目标是解剖信号通路，PA利用AP转化为BL膜在AP进入上皮细胞。我们概述了两个具体的目标，剖析PA的结合和PI 3 K的激活之间的信号通路。在目标1中，我们采用候选蛋白的方法，并探讨特定的宿主受体和非受体酪氨酸激酶在PA介导的PI 3 K活化和AP膜中的变化中的作用。这些候选基因中有许多是在父母资助的RNAi筛选中鉴定出来的。在目标2中，我们概述了两种互补的方法来识别宿主蛋白质，其酪氨酸磷酸化响应于PA结合到极化MDCK细胞的AP表面而发生变化。这些研究将提供一个机制的洞察PA附着到宿主细胞上皮细胞后引发的内化过程。他们将确定细菌用来致病的宿主因素。在分子水平上阐明PA-宿主细胞相互作用将为开发新的药物打开大门，这些药物不是针对病原菌本身，而是针对其用于入侵和引起疾病的关键机制。这项研究将主要在乌拉圭蒙得维的亚巴斯德研究所与Arlinet Kierbel合作完成，作为NIH批准号R 01 AI 065902的延伸。7.公共卫生相关性：铜绿假单胞菌是人类最致命的条件致病菌之一，是多种急性和慢性感染的病原体。我们正在研究这种细菌如何通过破坏宿主细胞机制来感染上皮细胞。新发现的与假单胞菌感染相关的宿主细胞蛋白质有可能作为新的药物靶点。

DESCRIPTION (provided by applicant): The ability of microbial pathogens to overcome the normally highly polarized host mucosal epithelial barrier is an early and critical step in pathogenesis. This is particularly critical for opportunistic pathogens such as Pseudomonas aeruginosa (PA), one of the most virulent opportunistic pathogens of man. In the setting of epithelial injury and loss of cell polarity PA can effectively colonize the mucosal surfaces, cause further damage, and disseminate. We have recently discovered that binding of PA to the apical (AP) surface of cultured epithelial cells induces a cell reprogramming process in which the local plasma membrane transforms from apical (AP) to basolateral (BL) membrane, generating a microenvironment that facilitates bacterial colonization and entry into epithelial cells. We have demonstrated through a large body of evidence that activation of Phosphoinositide 3-kinase (PI3K) is a key step in this process. A very important question that has not been addressed is what is the signaling pathway that is activated upon binding that results in bacterial uptake and creation of this new microenvironment. PI3Ks are adapted to receive regulatory input from protein tyrosine kinases or tyrosine phosphorylated proteins. It is known that PA infection of epithelial cells induces changes in the tyrosine phosphorylation status of host proteins. We hypothesize that PA infection of epithelial cells causes a tyrosine phosphorylation signaling cascade leading to activation of PI3K. Our long-term goal is to understand how PA interacts with host cells and causes disease. Our short-term goal is to dissect the signaling pathway that PA utilizes to transform AP into BL membrane during AP entry into epithelial cells. We outline two specific aims to dissect the signaling pathway(s) between binding of PA and activation of PI3K. In aim 1, we take a candidate protein approach and explore the role of specific host receptor and non-receptor tyrosine kinases in PA-mediated activation of PI3K and resultant changes in the AP membrane. Many of these candidate genes were identified in the RNAi screen that was carried out in the parent grant. In aim 2, we outline two complementary approaches to identify host proteins whose tyrosine phosphorylation changes in response to PA binding to the AP surface of polarized MDCK cells. These studies will provide a mechanistic insight into the process of internalization triggered by PA after attachment to the host cell epithelium. They will identify host factors that the bacteria exploit to cause disease. The elucidation of PA-host cell interactions at the molecular level will open the door for the development of new drugs that target not the pathogenic bacteria itself but the key mechanisms that it uses to invade and cause disease. This research will be done primarily in Uruguay at Institut Pasteur de Montevideo in collaboration with Arlinet Kierbel, as an extension of NIH Grant No. R01AI065902. 7. Public Health Relevance: Pseudomonas aeruginosa is one of the most virulent opportunistic pathogens of man and is the causative agent of a variety of acute and chronic infections. We are investigating how this bacterium infects epithelial cells by subverting the host cell machinery. New identify host cell proteins involved in Pseudomonas infection can potentially be used as novel drug targets.