Mobilization of lysosome anti-microbial defenses by the unfolded protein response

描述（由申请人提供）：专职吞噬细胞在抗微生物防御中发挥关键作用。通过吞噬作用摄取微生物导致形成动态囊泡隔室，称为吞噬溶酶体。吞噬溶酶体在物理上和功能上定义了微生物与宿主细胞的关键分离，允许宿主将降解性抗微生物机制靶向该密闭空间。我们发现细菌感染触发未折叠蛋白反应（UPR），这是一种与ER应激和先天免疫功能相关的细胞程序。UPR的激活增加了细胞降解蛋白质的能力，但这种降解的机制还不完全清楚。我们的初步研究表明，在细菌感染过程中UPR激活的结果增加与耐甲氧西林金黄色葡萄球菌（MRSA）的降解溶酶体区室和细菌杀灭的关联。特异性UPR调节剂的抑制导致与溶酶体的结合减少和MRSA杀伤减少。该提议的中心假设是，吞噬细胞中UPR的激活导致吞噬溶酶体网络的运输和降解能力增加，导致降解功能增强，从而增强抗微生物功能。为了验证这一假设，我们将（1）使用UPR激活后的物理和功能标志物测量溶酶体网络的动员;（2）定义UPR传感器Ire 1，ATF 6和PERK在感染期间响应先天免疫信号调节溶酶体运输和功能的特定方面的作用。通过UPR调节细胞的降解能力是细胞可以响应蛋白质产生或分泌中的扰动的基本策略。我们的研究现在强调了UPR介导的降解和抗微生物功能之间的新联系，并将定义关键的可药用靶点，这些靶点塑造了巨噬细胞抗微生物武器库，用于开发抗感染策略。 公共卫生相关性：毒性病原体可能逃避宿主的抗菌防御，是全球发病和死亡的主要原因。我们的研究揭示了一种基本的细胞应激反应，它广泛地增强了宿主的防御能力，增加了免疫细胞对耐甲氧西林金黄色葡萄球菌等细菌的杀伤。这些发现强调了抗微生物防御的新机制，可能为开发抗感染疗法提供潜在靶点。

DESCRIPTION (provided by applicant): Professional phagocytes play a critical role in anti-microbial defense. Uptake of microbes by phagocytosis results in the formation of a dynamic vesicular compartment, termed the phagolysosome. The phagolysosome physically and functionally defines a critical separation of the microbe from the host cell, allowing the host to target degradative anti-microbial mechanisms to this confined space. We find that bacterial infection triggers the unfolded protein response (UPR), a cellular program associated with ER stress and innate immune function. Activation of the UPR increases the capacity of the cell to degrade proteins, but the mechanisms responsible for this degradation are incompletely understood. Our preliminary studies suggest that UPR activation during bacterial infection results in increased association of methicillin resistant Staphylococcus aureus (MRSA) with the degradative lysosomal compartment and bacterial killing. Inhibition of specific UPR regulators results in decreased association with lysosomes and decreased MRSA killing. The central hypothesis of this proposal is that activation of the UPR in phagocytes results in increased trafficking and degradative capacity of the phagolysosomal network, leading to enhanced degradative, and thus anti-microbial, function. To test this hypothesis, we will (1) measure mobilization of the lysosomal network using physical and functional markers upon activation of the UPR; (2) define the role of the UPR sensors, Ire1, ATF6 and PERK in regulating specific aspects of lysosomal trafficking and function in response to innate immune signals during infection. Regulation of the degradative capacity of the cell by the UPR is a fundamental strategy by which cells can respond to perturbations in the production or secretion of proteins. Our studies now highlight a novel connection between UPR-mediated degradation and anti-microbial function, and will define key druggable targets that shape the macrophage anti-microbial arsenal for development of anti-infective strategies. PUBLIC HEALTH RELEVANCE: Virulent pathogens may evade host-antimicrobial defenses and are a major cause of morbidity and mortality worldwide. Our studies have revealed a fundamental cellular stress response that broadly enhances host defense, increasing killing of bacteria such as methicillin-resistant Staphylococcus aureus by immune cells. These findings highlight a new mechanism for anti-microbial defense that may provide potential targets for development of anti-infective therapies.