The Role of NKG2D/DAP10 in Toxoplasma gondii Infection

NKG2D/DAP10在弓形虫感染中的作用

• 批准号: 7360593
• 负责人: Rachel Margaret Presti
• 金额: $ 10.97万
• 依托单位: WASHINGTON UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-02-01 至 2011-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7360593
• 关键词: Adaptor Signaling Protein; Animal Model; Animals; Apicomplexa; Babesia; Bioterrorism; CD8B1 gene; Categories; Cell Line; Cells; Cessation of life; Cryptosporidium; Cyst; Data; Dendritic Cells; Disease; Disease Outbreaks; Dose; Environment; Epithelial Cells; Felis catus; Food; Food Supply; Genetic Models; Grant; Hematopoietic; Human; Ileitis; Immune response; Immunity; Immunohistochemistry; Immunologic Receptors; Immunology; In Vitro; Infection; Inflammation; Inflammatory; Inflammatory Bowel Diseases; Inflammatory Response; Inflammatory disease of the intestine; Ingestion; Interleukin-10; Interleukin-12; Intestinal Diseases; Intestines; Kinetics; Lead; Libraries; Ligands; Lymphocyte; Malaria; Measures; Meat; Mediating; Messenger RNA; Modeling; Mouse Strains; Mucosal Immunity; Mus; Natural Immunity; Natural Killer Cells; Nature; Necrosis; Oocysts; Oral; Parasites; Parasitic infection; Plasmodium; Predisposition; Production; Protozoa; Protozoan Infections; Public Health; Recruitment Activity; Regulation; Relative (related person); Reporter; Research Personnel; Risk; Role; Secondary to; Signal Transduction; Spleen; Stress; T-Lymphocyte; Testing; Thinking; Tissues; Toxoplasma; Toxoplasma gondii; Toxoplasmosis; United States; Wild Type Mouse; Work; antimicrobial; cell transformation; cell type; cytokine; cytotoxicity; enteritis; experience; genetic manipulation; human disease; immune function; insight; intraepithelial; macrophage; novel; novel therapeutics; oral infection; oral pathogen; pathogen; programs; receptor; response; tool; waterborne

DESCRIPTION (provided by applicant): Food and waterborne protozoal infections are a common cause of severe human disease worldwide. The Apicomplexa consist of numerous protozoa which cause disease, including Plasmodium, Toxoplasma, Cryptosporidia, and Babesia. Toxoplasma gondii is a Category B Priority pathogen which has an excellent small animal model, and is amenable to genetic manipulation. Oral infection with T. gondii in susceptible mouse strains results in inflammation and ileitis. In studies evaluating innate immunity to T. gondii, we have identified the signaling adaptor protein, DAP10, as important in protecting mice from lethal infection, toxoplasma replication, and ileitis. DAP10 is the signaling adaptor for the activating immunoreceptor NKG2D, which recognizes ligands on stressed, infected and transformed cells. Mice deficient in DAP10 express NKG2D on NK cells, but not on CD8+ T cells or gamma/delta-T cells. These mice are more susceptible to oral challenge with T. gondii. DAP10-/- mice have more severe intestinal inflammation and necrosis, higher parasite burdens in the spleen, and succumb to infection at doses of T. gondii which wild type mice routinely survive. Studies outlined in this proposal aim to determine whether the increased susceptibility of DAP10-/- mice is due to increased replication of T. gondii in the intestine due to lack of immune response by DAP10 expressing CD8+ T cells, macrophages and dendritic cells, or due to intestinal necrosis secondary to the loss of NKG2D/DAP10 mediated regulatory function of CD8+ T cells in the intestine. We will also directly test the hypothesis that the increased susceptibility in DAP10-/- mice is due to lack of NKG2D signaling. These studies will further delineate the innate immune response to oral challenge with T. gondii, and provide important insights to apicomplexan immunology as well as mucosal immunity to oral pathogens. Relevance to public health: Toxoplasma gondii is a common and important human pathogen, and is a model for other protozoal pathogens, including malaria. We have identified the activating immune receptor, NKG2D, as important for the natural, innate immune response to pathogens. Studies in this grant aim to define its role in oral infection with T. gondii.

描述（由申请人提供）：食物和水传播的原生动物感染是世界范围内严重人类疾病的常见原因。顶复合体由许多致病的原生动物组成，包括疟原虫、弓形虫、隐孢子虫和巴贝虫。刚地弓形虫是B类优先病原菌，具有优良的小动物模型，易于遗传操作。易感小鼠口腔感染弓形虫可引起炎症和回肠炎。在评估弓形虫先天免疫的研究中，我们已经确定了信号适配器蛋白DAP10在保护小鼠免受致命感染、弓形虫复制和回肠炎方面发挥重要作用。DAP10是激活免疫受体NKG2D的信号转接器，其识别应激、感染和转化细胞上的配体。缺乏DAP10的小鼠在NK细胞上表达NKG2D，而在CD8+ T细胞或γ / δ T细胞上不表达NKG2D。这些小鼠更容易受到弓形虫的口腔攻击。DAP10-/-小鼠有更严重的肠道炎症和坏死，脾脏中的寄生虫负担更高，并且在野生型小鼠通常存活的剂量下死于弓形虫感染。本提案中概述的研究旨在确定DAP10-/-小鼠易感性增加是由于表达CD8+ T细胞、巨噬细胞和树突状细胞的DAP10缺乏免疫应答导致肠道内弓形虫复制增加，还是由于NKG2D/DAP10介导的肠道内CD8+ T细胞的调节功能丧失继发于肠道坏死。我们还将直接验证DAP10-/-小鼠易感性增加是由于缺乏NKG2D信号的假设。这些研究将进一步描述弓形虫对口腔攻击的先天免疫反应，并为口腔病原体的顶复合体免疫学和粘膜免疫提供重要见解。与公共卫生的相关性：刚地弓形虫是一种常见和重要的人类病原体，是包括疟疾在内的其他原生动物病原体的模型。我们已经确定了激活免疫受体NKG2D，它对病原体的自然先天免疫反应很重要。本研究旨在确定其在弓形虫口腔感染中的作用。